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Regarding sample size and sampling methods. It is a common practice by

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us Indians that whenever we go to the grocery store or whenever

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we go to the vegetable or fruits market, before buying a whole

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lot of vegetables, we are tend to examine a

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sample of the whole lot of the things that we need to

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buy. Say for example, in this case, in this photograph, the person

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is trying to assess the quality of the wheat by taking

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few grains of wheat. Okay, so this is nothing but what is

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the concept of sampling in medical research. In medical research, what

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we want to do is we want to check the

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sample for doing medical research. Okay, whenever whenever we have

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a target population and we want to do a research related to

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any particular medical uh field. For example, say

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one doctor wants to conduct a research on the diabetes and

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say the foot ulcers in diabetes. Okay, so the target population will

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be the adult cases of diabetes and he

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wants to check how many diabetes cases they have foot

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ulcers. So what he will do? It is not necessary to target

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all the diabetes cases in his field practice area. Say for example,

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he is practicing in a city of Mumbai. So in the city

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of Mumbai, there will be thousands and lakhs of people who will

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be having diabetes. We just want to check how how much is

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the percentage of diabetes cases who are having foot ulcers. So what

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he will do? He will gather few of the patients from

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the Mumbai who are already diagnosed diabetic and he will conduct his

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research. he or she will conduct his the research on this few

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number of cases of diabetes. So this is the concept of sampling.

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In sampling, we want to do a particular research regarding a particular

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medical topic or any medical or social or any topic that we

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want to do research in that community, in that population. It is

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not necessary, it is not important to include all the patients or

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all the participants from the population. We can just take few of

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them and we conduct the research. Sampling, it is a scientific method

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by which some members of the population are selected as representatives

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of the entire population. It is a significant stage of scientific work

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and if ignored, the results may become invalid and futile. So it

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is one of the core part of research of in the medical

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field. So if we avoid scientific sampling method and if we

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fail to mention how the sample was sample size was calculated and

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how we came to a conclusion for this research that this much

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sample is sufficient, then it may be invalid and all

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the research may go in vain. The common terms in the sample

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sampling technique is the population. Population is the entire set of individual

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or objects having some common characteristics. Finite population, all units

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can be counted before sampling. Infinite all units cannot be enlisted.

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Now population is the whole method in which the sampling sample

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size can be there. Sampling is a small section or

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a subset of population selected to participate in the study. Now

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what is mean by sampling? Sample is a small section and sampling

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is the process of selecting subjects who are representative of the population.

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That is the difference between sample and sampling. Sample is the exact

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number of cases, exact number of participants that we will be taking

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into our study while sampling is the process of selecting these cases

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or process of selecting these samples. So here we have the target

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population in which that study will be done. Here we have

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study population which will be accessible. Study population is the population

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that will be accessible, will be available to be included in the

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study and from this study population, we will include this sample,

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these few cases in our research. Okay, so that is the basic

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concept behind selecting the number of cases, number of participants for a

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research in the sampling. So the target population is

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the population where we want to generalize our finding. Say for example,

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in that diabetes foot ulcer study in the city of Mumbai, the

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doctor finds out that out of the 200 cases of diabetes studied,

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there were 40 cases of foot ulcers. That means the foot ulcer

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percentage is 20% in the diabetic cases. And this 20%

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prevalence of foot ulcer in diabetic, it can be generalized in the

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target population of the all the diabetes cases in the city of

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Mumbai. So we can say that in the city of Mumbai, there

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is a prevalence of 20% of diabetic foot ulcers in

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the cases of diabetes. Even though we have just studied 200 cases

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of diabetes, there can be thousands and lakhs of cases in the

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city of Mumbai. Similarly, we can generalize this on even larger

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scale. The study population is the population that you get access to

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and the sample is the exact number of cases, the person

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that we have conducted the study on. Study population depends on the

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research question, how many injections do people receive each year in India?

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Okay, so what will be the study population in this case? It

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will be the population of India. If the study population we

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need to see how many needle stick healthcare workers experience each

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year in India. So what are the needle stick injuries? Say for

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example, a nurse is collecting blood sample of a patient. Accidentally,

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what happens is after collecting the blood sample, the needle gets pricked

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to the hand of the nurse. So what is this? This is

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a needle stick injury. So we want to know how many needle

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stick injuries are there to the healthcare workers each

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year. So the study population will be healthcare workers of India. If

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we want to know how many hospitals have a needle stick prevention

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policy in India, what will be the study population? It will be

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the number of hospitals in India. So this is the way we

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from the research question, we can decide what will be our study

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population. Why sampling is required? It is required to obtain information from

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large populations and to ensure the efficiency of a study. To

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obtain more accurate information, we we do the sampling. The

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sampling terms are sampling unit or basic sampling unit which is the

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elementary unit that will be sampled. Okay, so this sampling unit in

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the study where we wanted to know how many hospitals have

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the needle stick injury policy. Here the sampling unit will be a

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single hospital. Okay, a single hospital will be the elementary unit.

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It will not be any patient in that hospital or any doctor

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in that hospital because our research question is how many hospitals have

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needle stick injury policy. So here elementary unit will be the one

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single hospital. In the in the study of the diabetic foot foot

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ulcers in the city of Mumbai, elementary unit of the research will

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be one patient of diabetes in the state in the city of

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Mumbai. Okay. So these are these can be people, these can be

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healthcare workers, these can be hospitals. Okay, so as I have explained

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what is the sampling frame? It is the list of all sampling

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units in the population. The sampling scheme, it is the method used

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to select sampling units from the sampling frame. So now we know

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what is sampling unit. Sampling frame, we need to have a list

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of all the sampling units in the population. If we want to

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study the number of hospitals with needle stick injury policy, we need

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to have a list of all the hospitals in that particular area

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where we want to conduct our study. Say for example, in India,

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we need to have list of all the hospitals in India. If

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we want to study the diabetic foot foot ulcer, we need to

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have a list of all the diabetes cases in the city of

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Mumbai. Sampling scheme is the method used to select sampling units from

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the sampling frame. So sampling scheme is how exactly we are going

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to select those 200 diabetes cases from the city of Mumbai who

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who may have thousands and lakhs of diabetes patients. Okay. So how

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exactly are we going to select this diabetes cases? Is

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the sample representative one in terms of time, place and person? What

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does it mean representative? That means the 200 cases that

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we have chosen in our study for diabetes, it should be similar

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to all the say for example, there are 200,000 cases of diabetes

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in the study of in the city of Mumbai. Out of 200,000

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diabetes cases, we have we have taken the 200 cases of diabetes

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for our research. So we are taking 0.1% of

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the whole number of diabetes cases. 200,000 200 divided by 200,000

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into 100 taken into percentage is 0.1

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percent. Okay. So in terms of time, whether all

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have diabetes for a similar duration, whether all are residing in

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the urban like urban slums or in the high rise area

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or in the high income group areas. And in the terms of

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person, whether the male and female distribution, age distribution is similar in

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the 200 cases that we are going to study as compared to

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the 200,000 population. So it is the whether the sample is representative

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one. For example, the Ministry of Health of a country X wants

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to estimate the proportion of children in elementary schools who have been

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immunized against childhood infectious diseases. So we have various childhood infectious

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diseases and in a country the Ministry of Health wants

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to see how many percentage of children in elementary schools are

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immunized. The task must be completed in a month. We have only

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one month. The objective is to estimate the proportion of immunized children.

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The types of sampling. So here what is the challenge, biggest challenge

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is in just one month, we cannot see the

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whole country. The whole country will have lakhs and crores of

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children going to the elementary school. but in one month, we can

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just do a few number of schools and we can check few

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number of children only. The types of sampling are broadly classified into

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probability sampling and non-probability sampling. Probability sampling we have simple random

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sampling, stratified random sampling, systematic sampling and cluster sampling,

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multi-phase and multi-stage sampling. Non-probability sampling we have purposive, quota,

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snowball sampling, sequential sampling, convenience sampling. Okay. So this is

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the basic difference between probability and non-probability sampling. As the

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name suggests, probability sampling it has got a every

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person, every individual, every unit, every sampling unit in the sampling

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frame will have a nth probability

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of getting selected in the probability sampling. While non-probability sampling, there is

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no any such probability that there is no any particular

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formula or particular figure where the samples will be selected. Okay, so

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that is the basic difference. What is probability sampling? Sampling method where

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every member of the population has an equal chance of being selected

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as a sample. Only sampling method that allows to draw valid conclusions

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about a population. Random sampling which is the first in

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case of probability sampling. It removes possibility of bias in selection of

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subjects. Okay, what is bias? Bias is the mistake that can occur

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in the selection of subjects. Random sampling ensures that each subject has

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a known probability of being chosen and it allows application of statistical

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theory. The sampling error no sample is perfect mirror image of the

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population. Magnitude of error can be measured in probability samples expressed

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as a standard error of mean proportions or differences and functions of

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sample size and variability in measurement can be done by sampling error.

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What is simple random sampling principle? There is equal chance for each

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sampling unit procedure. First, we need to number all the units and

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then we need to randomly draw units. Okay, so we have 200,000

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cases of diabetes in the city of Mumbai. What we do is

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we enlist and we number all the 200,000 cases of diabetes from

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1 to 200,000 and if our sample size is 200, what we

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do is we randomly draw the 200 numbers in from

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these 200,000 samples. Okay. Advantage it is a simple and sampling

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either is easily measured. Disadvantages we need complete list of units and

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it does not achieve best representation. Okay. So there is a a

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simple random sampling and the random numbers can be obtained

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from the biostatistics books, research methodology books where the random numbers list

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will be provided or we can just go to the software for

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biostatistical research, medical research which is EP info and

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the website calculations are also available online on the EP info. So

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after the end of this lecture, we will see how we can

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get the random number list from the EP info software and

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we will also do one sample size calculation in the software.

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Okay, so this is the example of simple random sampling. Here we

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have 1 to 48 list and out of these 1 to 48

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randomly we are selecting these four cases. So number nine Dennis, number

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18 Frank, number 32 Mike, number 40 LM we are selecting

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in our sample. What is systematic sampling? A unit drawn every

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K unit. So here we have a number which repeats and

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we take every that number. Equal chance of being drawn

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from each unit procedure. First, we need to calculate the sampling interval.

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K is equal to N by N. So what is this sampling

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interval? For example, in the diabetes studies, we have 200,000 diabetes cases.

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Capital N is the whole population. It is 200,000. Small N is

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our sample size. It is 200. So 200,000 by 200 that will

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be 1,000. We need to see a random number of less than

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K that is less than 1,000 for starting. Say for example, our

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random number is 125. So this is a random number 125.

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Every K unit from the first unit, we can select and we

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can prepare a sample. So 125 plus

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the first patient will be 125 number. Second patient will be

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1,125. Third patient will be 2,125. Fourth

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number will be 3,125 because K or the sampling interval

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here is 1,000. That means out of 200,000 patients, we need

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to have 200 diabetes cases and for that sampling interval of 1,000

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is there. When we have selected a random number of 125 after

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125 which which is the first case, first patient to be included

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in the study. Every 1,000 case we will be adding to our

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research. Advantages ensures representativeness across list and easy to implement.

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Disadvantage dangerous if the list has got cycles. Example of systematic sampling

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if we want to study households which have got supply of clean

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drinking water. We have selected the a colony

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and we have found our sampling interval which is eight house or

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the sampling interval is eight. We started with the third house or

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the number three house and we went to the three plus eight.

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1 2 3 4 5 6 7 8. This is the 11th

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house. So this is the sampling interval eight 11th house we will

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be adding. Again, we will go eight house one 1

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2 3 4 5 6 7 8. 19th house we will add

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again the 27th house, then 35th house,

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then 43rd house, then 51st house. So upper like

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this every eighth house we will be adding in our research. Now

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what is stratified sampling? So this was systematic random sampling. Okay. This

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is now stratified sampling. What is stratified sampling? Principle is to classify

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population into homogeneous groups like strata. Draw a sample in each strata

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and combine these results of all strata. Advantages it is a more

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precise if variable associated with the strata. All subgroups are represented

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allowing separate conclusions about each of them. Disadvantage sampling error is difficult

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to measure. Loss of precision if small numbers sampled in individual

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strata. Example of stratified sampling are to estimate vaccination

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coverage in a country. One sample drawn in each region and then

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estimate calculated for each strata. Okay, so we need to divide the

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sample into different strata. So for vaccination coverage

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in the country, we have to draw one sample from each region

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in region of Northern India, Western India, Eastern India, Southern India, Northeast

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states. So we have divided five regions and we take samples

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from each region and we calculate the estimate from

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each strata. Each strata weighed into obtain estimate for

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a country. Now what is cluster sampling? Principle is the random samples

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of groups or clusters of units are to be included in the

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study. All or proportion of units are included from the selected clusters.

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Advantage it is simple, no list of units required and less travel

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or resources are required. Let me give you an example of a

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cluster sampling for our Indra Dhanush project that we have done a

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few years back. What we needed to do is we need we

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needed to check the immunization status of a district. What we

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did was we made a clusters of seven villages

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in that district and from the each cluster we selected 30 cases

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of children under five years of age. So what what was the

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advantage? We didn't require any list of all the children of all

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the villages. We just selected seven random villages and we went into

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those villages and we selected 30 random children of less than five

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years of age from each village. So this is a cluster sampling

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where we are taking the clusters of seven different villages and in

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that one cluster we are taking 30 cases. Disadvantages imprecise

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if clusters are homogeneous and sampling either is difficult to measure. The

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sampling unit is not a subject but a group of subjects. So

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that every group of 30 children under five from the villages was

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the sampling unit. It is assumed that the variability among clusters is

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minimal. The variability within each cluster is what is observed in the

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general population. Two stages of cluster sampling first stage is probability proportional

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to the size. Select the number of clusters to be included. Compute

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a cumulative list of the populations in in each unit with a

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grand total. Divide the grand total by the number of clusters and

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obtain the sampling interval. So how exactly we come to know

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about how many villages are to be included? For that, we need

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to have the number of clusters, the total number of villages that

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will be available in that district. Say for example, there were 140

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villages in that district. And we we got

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the sampling interval of 20. So for every

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one village, for every 20 villages, we had to study one village

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for that particular study. The sampling interval being 20 and total number

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of villages in the district was 140. So we divided 140 by

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the sampling interval 20. So we got a cluster sample of seven.

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Okay. Choose a random number and identify the plus first cluster. So

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we name all the number, all the villages 1 to 140

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and we start with the third village and every seventh every 20th

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village we go and we take the sample. So third, 23rd,

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43rd, 63rd, 83rd like that we chose seven

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villages. Add the sampling interval and identify the second cluster. By repeating

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the same procedure, identify all the clusters. And the second stage is

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in each cluster select a random sample using a sampling frame of

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subjects or households. So same way in the village also we can

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select by different random number sample. You can select those

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30 cases each. This was all regarding the cluster sampling. Now what

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is multi-stage sampling? As the name suggests, it has got stages. So

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this is the stage one some part of those who are in

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the stage one will go to the stage two. Some part of

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those who are in the stage two will go to the stage

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three. So this is a stage wise sampling. Principle is several

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chained samples are required and several statistical units are required. Advantage is

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no complete list of population is required and more feasible approach for

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large population. Disadvantage several sampling lists we have to make and sampling

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error is difficult to measure. So this multi-stage camp sampling

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we from India, we choose three states 1 2 3 and

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we exclude these two states and from this one state we choose

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three districts 1 to 3 and from these three districts we choose

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one district and we include these three villages from that district from

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the whole country of India. So this is from the India we

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choose. So out of total 27 villages we have chose

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these three villages from these nine districts from these total three states

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in the country of India. So this is the way we go

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in the multi-stage sampling. Multi-phase sampling, sampling is done in different phases.

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Part of information is collected from whole sample and part of information

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from sub-sample. Here each sample is adequately studied before another sample is

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drawn from it. Example a tuberculosis study. Tuberculosis multi-phase

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study phase one first Mantoux test was done to all

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the cases who are suspected of tuberculosis. Out of those who are

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Mantoux positive, we will conduct X-ray, chest X-ray.

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So what will happen? Mantoux test will be positive in suspected cases

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of tuberculosis. Those who are negative Mantoux test, we will not add

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them in the phase two. We will add only those who are

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Mantoux test positive for the phase two. In the phase two, we

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will do their chest X-ray. For phase three, those who are chest

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X-ray positive only we will go for the sputum examination.

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It will be either sputum microscopy or it will be the CBNAAT

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assessment of the sputum which is the cartridge-based nucleic acid amplification test.

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So this is the phase-wise sampling. Those who need sputum examination will

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be small as compared to to all the cases that we have

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studied by doing the Mantoux test, okay? So the difference between multiplex

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and multi-stage is multi-stage sampling frame is different at each state while

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multi-phase is samples are drawn from the same phase. It is used

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when insufficient budget to collect data from the whole sample is available.

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So this was all about the probability sampling. Now coming to the

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non-probability sampling, please remember for hospital-based studies,

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the most common type of sampling method used are non-probability sampling. For

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community studies, for epidemiological studies, for field research, it is very important

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that the type of sampling method used is probability sampling. A community-based

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study which is being which is used which is done using non-probability

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sampling is not a very good type of medical research. So for

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community-based studies, probability sampling are the best method of sampling to be

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used and for hospital-based studies, we can use non-probability sampling or

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for few of the particular studies also we use non-probability sampling. We

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will just go through them. It is a non-scientific sampling method. Every

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member of the population is not given a chance to be part

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of the sample. Choice depends on judgment of the researcher. What is

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judgment sampling? It is a purposive or deliberate sampling. Quota

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sampling, selecting 10 patients from each port. So quota sampling is we

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need to see what is the patient satisfaction regarding the services provided

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in the hospital. So for that, what we do is we select

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10 cases from each ward, 10 from the medicine male ward, 10

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from the medicine female ward, 10 from the gynecology ward, 10 from

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the surgery male, surgery female, 10 from the ortho male, orthopedic female,

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10 from the pediatric male and female. So we have this quota

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sampling. This is stratified sampling minus randomization. Sequential

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sampling, it is a consecutive sampling. Number of samples are drawn one

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after another from the population. We need to study what are the

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complications in diabetes. So so

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sequential sampling, what we do? The complications in the cases of diabetes

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in a hospital we want to study. What we will do? We

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will we will take the patients patients of diabetes as they come

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in the hospital one hour after the another. Now what is snowball

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sampling? Initial sample is selected by probability method and additional samples are

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obtained by referral from the initial respondent. So snowball sampling is a

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first a small proportion of samples we select by probability

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method and because of the rare form of these cases

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or the difficult to get the samples, we what we do is

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we refer the other cases to known cases from this first

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initial sample, okay? So I remember a snowball sampling method that we

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had done for the adolescent boys who are involved in

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the intravenous drug abuse in the urban slums of Mumbai. So that

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was one of the researches that we carried out and what we

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did is we identified four or five boys by the probability sampling

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method who were known intravenous drug abusers and

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we took them into confidence. We told them that no

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any legal action will be taken. We are just doctors. We want

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to inquire why you are all behind this and we want to

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help you, okay? So then they opened up and then they told

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okay, so I have two friends living in this jhopdi. I have

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two friends living in this gully. They also are habituated for

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the intravenous drug abuse. So this is how the number of samples

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by this referral from these close circuits went on increasing

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and this is how we conducted this snowball sampling. It is useful

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in locating rare cases. Then we have census sampling or universe sampling.

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A study using all available elements or members of a population. Say

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for example, we need to know what is the average

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height of the medical students admitted to a medical

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college. So what we will do? We will include all the MBBS

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00:31:00.530 --> 00:31:04.130
students who have been admitted in a particular medical college in a

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city. Say for example, there are 200 per batch and there are

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00:31:08.930 --> 00:31:13.030
four MBBS batches and one interns batch. So we have 1,000 medical

392
00:31:13.030 --> 00:31:16.430
students in that medical college. So what we will do? We will

393
00:31:16.530 --> 00:31:20.830
use universal method of sampling and we will include all the 1,000

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00:31:20.830 --> 00:31:25.630
cases, all the 1,000 medical students for checking their mean height. When

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00:31:25.630 --> 00:31:30.630
your population is very small, when you have extensive resources and

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00:31:30.630 --> 00:31:34.030
when you don't expect a very high response. So what will you

397
00:31:34.030 --> 00:31:38.430
do? We include all of them in the study. Convenience sampling, what

398
00:31:38.430 --> 00:31:42.430
we mostly use in our studies? The samples are included as per

399
00:31:42.430 --> 00:31:48.730
the convenience of the researcher and so the merits of probability

400
00:31:49.130 --> 00:31:53.830
the convenience sampling are it is easy to obtain the sample and

401
00:31:53.830 --> 00:31:57.830
effective in testing the instruments and used in qualitative studies and demerits

402
00:31:57.830 --> 00:32:02.930
of non-probability sampling are they lack generalization, no representativeness and there

403
00:32:02.930 --> 00:32:06.830
is a sampling error. Now before going to the sample size calculation,

404
00:32:06.830 --> 00:32:11.930
there is a question. Diya asked where the biases

405
00:32:11.930 --> 00:32:16.930
which may arise in systematic sampling especially with periodic patterns

406
00:32:16.930 --> 00:32:21.230
in the population. So what happens is whenever there is a systematic

407
00:32:21.230 --> 00:32:25.830
sampling we are going to conduct, still it may not be a

408
00:32:25.930 --> 00:32:30.130
total representative of the population because even if we are doing it

409
00:32:30.130 --> 00:32:34.730
systematically, even if we try to remove all the biases, there is

410
00:32:34.730 --> 00:32:38.830
a chance that the samples that we have collected, they are not

411
00:32:38.830 --> 00:32:45.330
exactly the representation of the whole sample, okay? So now just

412
00:32:45.930 --> 00:32:50.130
as I have told you that we need to get the random

413
00:32:50.130 --> 00:32:55.530
numbers from for the random sampling, okay?

414
00:32:55.530 --> 00:33:00.830
So systematic random sampling we need to have

415
00:33:01.430 --> 00:33:05.830
the random numbers, okay? So I'll just share all of you. Please

416
00:33:05.830 --> 00:33:11.530
open your web browsers so that you can also do it in

417
00:33:11.530 --> 00:33:16.630
real time, okay? I hope you all can see my screen. So

418
00:33:16.630 --> 00:33:25.330
here you have to go and type open API. Okay,

419
00:33:25.430 --> 00:33:28.630
so this is a menu for open API. It is a very

420
00:33:29.230 --> 00:33:34.630
nicely prepared software. It is also available online website for various

421
00:33:35.430 --> 00:33:44.130
statistical tools. Here we have the random numbers, okay? So

422
00:33:44.330 --> 00:33:48.030
if we want to this is an example, the random number general

423
00:33:48.030 --> 00:33:53.230
they have explained this module generates a specified number

424
00:33:53.230 --> 00:33:57.630
of random integrates within a given range. To obtain decimal results, generate

425
00:33:57.630 --> 00:34:01.030
integrates and then move the decimal point as needed. We don't need

426
00:34:01.130 --> 00:34:05.530
decimal results. What we need is we need a random set of

427
00:34:05.530 --> 00:34:10.830
numbers in a particular population, okay? So the random

428
00:34:10.830 --> 00:34:16.330
number generator lowest value will be one, highest value will be how

429
00:34:16.330 --> 00:34:21.730
many cases you need, okay? So say for example, we

430
00:34:21.730 --> 00:34:27.130
need a total of 200 cases from 1,000

431
00:34:27.130 --> 00:34:30.830
population. So the lowest value will be one, highest value will be

432
00:34:30.830 --> 00:34:36.230
1,000. How many cases are required? We require 200 cases and

433
00:34:36.230 --> 00:34:39.930
format into how many columns? So five columns is okay and then

434
00:34:39.930 --> 00:34:44.630
we say calculate. So here is a list of 200 random numbers

435
00:34:44.830 --> 00:34:49.930
from one to 1,000 population. So if in the 1,000

436
00:34:49.930 --> 00:34:55.430
medical students we want to conduct a study using simple random sampling,

437
00:34:55.630 --> 00:35:00.530
we can just enumerate the number of 1,000 number of students from

438
00:35:00.530 --> 00:35:05.230
one to 1,000. We need to add the roll number and name

439
00:35:05.330 --> 00:35:09.830
the students one to 1,000 and we can use this random sample

440
00:35:09.830 --> 00:35:14.430
generator from open API and you can code this in your research,

441
00:35:14.530 --> 00:35:18.730
okay? In the methodology, you need to code that for my research,

442
00:35:18.830 --> 00:35:24.030
I used random number generator from open API. You can just

443
00:35:24.030 --> 00:35:29.030
copy-paste this link and you can just copy-paste a screenshot

444
00:35:29.030 --> 00:35:33.030
of this in your project or you or for your article publication,

445
00:35:33.030 --> 00:35:38.030
you can just mention that you used the random numbers generated

446
00:35:38.030 --> 00:35:43.330
from the open API. Okay, let's take another example of the

447
00:35:43.330 --> 00:35:48.530
diabetes study. We want to include 200 cases. The highest value

448
00:35:48.530 --> 00:35:53.930
is 2 lakh. We have 2 lakh cases of diabetes. So

449
00:35:54.030 --> 00:35:58.130
one to 2 lakh and we need to calculate 200 cases of

450
00:35:58.130 --> 00:36:03.130
diabetes, okay? So here we have if we

451
00:36:03.130 --> 00:36:07.830
have a list of 2 lakh patients of diabetes and we want

452
00:36:07.830 --> 00:36:12.830
to include 200 cases here we can just include these numbers.

453
00:36:12.830 --> 00:36:17.830
So like number 41,976, number 4,499 will be

454
00:36:17.830 --> 00:36:21.830
included in the study. So this is the random number generator and

455
00:36:21.830 --> 00:36:27.030
that we need to okay. So there is one another question.

456
00:36:27.630 --> 00:36:32.730
How to account for variability in outcomes when calculating sample sizes for

457
00:36:32.830 --> 00:36:38.130
multi-center study, okay? So this is a very technical

458
00:36:38.130 --> 00:36:43.130
statistical question. It will require a long lecture

459
00:36:43.130 --> 00:36:48.230
or even longer lecture for the variability outcome calculator when

460
00:36:48.230 --> 00:36:53.230
calculating the sample sizes for multi-center study. But in multi-center studies

461
00:36:53.230 --> 00:36:58.430
also you can use different type of sampling method

462
00:36:58.430 --> 00:37:04.330
and that can be used for the multi-center study, okay? So

463
00:37:04.330 --> 00:37:10.030
next we will come we will do a small

464
00:37:10.130 --> 00:37:15.130
sample size calculation for a

465
00:37:15.130 --> 00:37:20.430
probability sampling and for a prevalence study, okay? So

466
00:37:20.730 --> 00:37:25.630
for sample sample size calculation for descriptive study, the formula for sample

467
00:37:25.630 --> 00:37:30.030
size calculation for a descriptive study is n is equal to p

468
00:37:30.730 --> 00:37:35.830
into one minus p in the bracket z by e squared, okay?

469
00:37:35.930 --> 00:37:39.230
So what are these symbols? We will come to know about that.

470
00:37:42.330 --> 00:37:47.430
p here is the estimate of expected proportion with the variable

471
00:37:48.230 --> 00:37:53.730
of interest in the population. So p

472
00:37:54.330 --> 00:38:00.130
what we have as a p is the estimate of expected proportion

473
00:38:00.130 --> 00:38:04.930
with the variable, okay? It can be a number. Say for example

474
00:38:05.230 --> 00:38:10.230
for the study of diabetic foot ulcers, we have the cases

475
00:38:10.230 --> 00:38:14.930
of diabetes. For that, we need either the proportion of diabetes in

476
00:38:14.930 --> 00:38:19.530
India or in urban slums or in in the Indian metropolitan city

477
00:38:19.830 --> 00:38:23.330
or the proportion of diabetes in the whole world. So any of

478
00:38:23.330 --> 00:38:26.430
these proportions we can use as a p. If it is in

479
00:38:26.430 --> 00:38:31.930
the form of percentage for 10 % we will use 0.1. For

480
00:38:32.030 --> 00:38:37.130
15.4 % we will use 0.154,

481
00:38:37.230 --> 00:38:42.330
okay? q here mentioned here will be the

482
00:38:42.430 --> 00:38:46.330
one minus p, okay? So the q stands for one minus p.

483
00:38:47.130 --> 00:38:51.030
e squared is e is nothing but the precision level. We can

484
00:38:51.030 --> 00:38:56.430
take the precision of 5%, 7% or 10% more

485
00:38:56.430 --> 00:39:01.330
than 10% we should not take the e or the precision level.

486
00:39:01.330 --> 00:39:05.130
5% is the ideal level of precision that can be included for

487
00:39:05.130 --> 00:39:10.330
the sample size calculation. Four is nothing but the z squared. z

488
00:39:10.330 --> 00:39:15.530
is the statistics for desired level of confidence that is 0.05

489
00:39:15.630 --> 00:39:20.730
which comes to 1.96 for 95% confidence interval.

490
00:39:20.730 --> 00:39:25.330
z is nothing but 1.96 which is rounded off to two. So

491
00:39:25.330 --> 00:39:29.830
the z square as per this formula z square will become four.

492
00:39:30.430 --> 00:39:34.830
So this formula in simple terms it is sample size n is

493
00:39:34.830 --> 00:39:38.830
equal to four into p into one minus p which is the

494
00:39:38.830 --> 00:39:43.030
q and divided by e square, okay? So this is the formula

495
00:39:43.030 --> 00:39:48.030
that you can mention in your research methodology that sample

496
00:39:48.030 --> 00:39:52.230
size calculation you will be using the formula for sample size calculation

497
00:39:52.230 --> 00:39:55.430
from the proportion which will be n is equal to four pq

498
00:39:55.430 --> 00:40:00.230
by e square. So majority of the studies that you conduct this

499
00:40:00.330 --> 00:40:05.330
formula will be applicable. Example, if we want to study the prevalence

500
00:40:05.330 --> 00:40:10.730
of diabetic retinopathy in an urban slum, the required proportion or

501
00:40:10.730 --> 00:40:14.130
p that we will be using either the prevalence of diabetes or

502
00:40:14.130 --> 00:40:19.130
prevalence of diabetes diabetic retinopathy from a research article and

503
00:40:19.330 --> 00:40:23.430
we can code this research article in your methodology in the sample

504
00:40:23.430 --> 00:40:28.430
size calculation that a research article conducted by in this

505
00:40:28.430 --> 00:40:33.230
case a kumar at all they have reported the prevalence of diabetes

506
00:40:33.230 --> 00:40:37.530
of 10.5 % which is the p is equal to 10.5 %

507
00:40:37.930 --> 00:40:43.130
which is equal to 0.105. q will be one minus p which

508
00:40:43.130 --> 00:40:48.330
will be 0.895 and considering the absolute error

509
00:40:48.330 --> 00:40:53.530
of 5% which will be 0.05. The sample size calculation here

510
00:40:53.530 --> 00:40:57.030
will be n is equal to four pq by e square. It

511
00:40:57.030 --> 00:41:03.730
will be four into 0.105 into 0.895

512
00:41:03.830 --> 00:41:09.130
divided by e square. The e that is 0.05 or 5%

513
00:41:09.130 --> 00:41:15.030
it will come to around 151. So we will code that a

514
00:41:15.030 --> 00:41:19.830
kumar at all reported prevalence of diabetes of 10.5 and we are

515
00:41:19.930 --> 00:41:24.030
taking the sample size for this prevalence of diabetic retinopathy in an

516
00:41:24.030 --> 00:41:29.430
urban slum. Sample size that will be taken is 151 or any

517
00:41:30.330 --> 00:41:35.730
any number larger than 151, okay? So if we have 160 eligible

518
00:41:35.730 --> 00:41:39.530
cases, we will include all the 160 cases. We will just add

519
00:41:39.530 --> 00:41:44.430
one line that the sample size calculated was 151 but we got

520
00:41:44.430 --> 00:41:49.230
larger number of cases than 151 like 160. So we included all

521
00:41:49.230 --> 00:41:53.230
the 160 cases or 200 cases in our study. The sample size

522
00:41:53.530 --> 00:41:57.730
calculated from this formula it should be the minimum sample size. At

523
00:41:57.730 --> 00:42:01.830
least 151 cases of diabetes should be included in the study. Less

524
00:42:01.830 --> 00:42:05.230
than that you cannot include but more than that yes we can.

525
00:42:06.330 --> 00:42:11.730
Okay? So the take home message for from this will be

526
00:42:11.730 --> 00:42:16.730
we cannot study the whole population. So we reduce it by in

527
00:42:16.730 --> 00:42:20.630
the terms of samples. Taking a sample leads to sampling error which

528
00:42:20.630 --> 00:42:25.830
is measurable, good design and quality assurance ensure validity and appropriate sample

529
00:42:25.830 --> 00:42:30.730
size will ensure precision. Probability samples are the only one that allow

530
00:42:30.730 --> 00:42:35.330
use of statistics as we know them and for further reading you

531
00:42:35.330 --> 00:42:40.330
can go and read textbook of on research guide

532
00:42:41.730 --> 00:42:45.830
where we have topics of sample size calculation and sampling methods in

533
00:42:45.830 --> 00:42:50.830
the research. Okay? So let's just take another example for

534
00:42:51.130 --> 00:42:56.330
the sample size calculation using the open API software, okay?

535
00:42:56.330 --> 00:43:01.530
So same website open API you can just mention you can just

536
00:43:01.530 --> 00:43:05.030
take a screenshot of this. For sample size calculation, you will be

537
00:43:05.030 --> 00:43:11.030
using openapi.com for random number calculation. You will also be using openapi.com,

538
00:43:11.030 --> 00:43:16.030
okay? So I'll just the same example we will take. I'll show

539
00:43:16.030 --> 00:43:20.430
you how we came to know about the prevalence of diabetes 10.5%

540
00:43:20.630 --> 00:43:25.030
using this article by a kumar at all review article by a

541
00:43:25.030 --> 00:43:30.230
kumar at all using Google Scholar and 151 we have come from

542
00:43:30.230 --> 00:43:34.230
using this formula but using EP info it will be a little

543
00:43:34.230 --> 00:43:39.430
bit less. So we'll just go and try. So stay with me

544
00:43:39.430 --> 00:43:44.430
for few more minutes. So

545
00:43:44.430 --> 00:43:49.630
we want to do an article. We want to do

546
00:43:50.530 --> 00:43:56.330
sample size. We want to check the sample size from the

547
00:43:56.430 --> 00:44:01.930
open API, okay? So here first I search

548
00:44:01.930 --> 00:44:06.430
about prevalence of diabetes in India in Google Scholar. Okay, this is

549
00:44:06.430 --> 00:44:09.930
not normal Google. This is Google Scholar or same way you can

550
00:44:09.930 --> 00:44:14.930
search in the PubMed. So we got different articles about epidemiology of

551
00:44:14.930 --> 00:44:19.130
type two diabetes, prevalence and trends of diabetes, high prevalence of diabetes,

552
00:44:19.430 --> 00:44:23.530
epidemiology of type two diabetes in India and this is the article

553
00:44:23.730 --> 00:44:26.730
by a kumar at all where there is a prevalence of diabetes

554
00:44:26.730 --> 00:44:31.230
in India reviews of ID of diabetes atlas 10th edition. When we

555
00:44:31.230 --> 00:44:35.030
open this link by a kumar at all, we got the prevalence

556
00:44:35.030 --> 00:44:41.530
of diabetes in India and they have reported that worldwide

557
00:44:41.530 --> 00:44:47.030
prevalence diabetes affects estimated 537 million adults worldwide,

558
00:44:47.030 --> 00:44:52.130
okay? And it is around 10.5% of all adults in this age

559
00:44:52.130 --> 00:44:57.430
range. So this is the 10.5% prevalence for diabetes

560
00:44:57.430 --> 00:45:01.130
in whole world, okay? So we can use this prevalence but more

561
00:45:01.230 --> 00:45:06.830
precise will be the number of diabetes cases in India, okay? Using

562
00:45:06.830 --> 00:45:10.630
this prevalence, what we will do is we will go to the

563
00:45:10.830 --> 00:45:14.930
open API menu. We will go to the sample size. We will

564
00:45:14.930 --> 00:45:20.830
go to the proportion. In the proportion, we

565
00:45:20.830 --> 00:45:23.730
will enter new data. So this is the sample size of a

566
00:45:23.730 --> 00:45:29.330
proportion and here they have explained how this module calculates

567
00:45:29.330 --> 00:45:33.930
the sample size from the proportion, okay? Now we go to the

568
00:45:34.230 --> 00:45:39.530
enter new data. For here we need population size. It is not

569
00:45:39.530 --> 00:45:44.530
important. It is not required to change this population size. If we

570
00:45:44.530 --> 00:45:48.430
know exact population, say for example in a city of Mumbai, you

571
00:45:48.430 --> 00:45:52.130
know that Mumbai city 2 crore people are there. You can enter

572
00:45:52.130 --> 00:45:56.430
2 crore people, okay? Or just leave it as it is. Anticipate

573
00:45:56.630 --> 00:46:02.630
anticipated frequency here. We have got anticipated frequency of 10.5%.

574
00:46:02.730 --> 00:46:08.830
So here it is in the percentage, okay? 10.5%. Confidence level, limit,

575
00:46:09.330 --> 00:46:14.030
percent or absolute precision. So this is absolute precision e which is

576
00:46:14.030 --> 00:46:18.730
5%. We need to keep it that way and this design effect

577
00:46:18.730 --> 00:46:24.330
also one we had to we have to keep see. So

578
00:46:24.430 --> 00:46:30.230
for a confidence interval of 95% the sample size comes to 145.

579
00:46:30.330 --> 00:46:35.330
What we calculated was 151. It was because we have

580
00:46:35.430 --> 00:46:40.530
taken z square as four, okay? Actually z

581
00:46:40.530 --> 00:46:46.330
square is 1.96 into squared which comes to around 3.84

582
00:46:46.330 --> 00:46:51.230
some, okay? But because of that this five six number of cases

583
00:46:51.230 --> 00:46:55.830
more we have got by that formula four pq by e square.

584
00:46:55.930 --> 00:47:00.030
So this is the 95% sample size that we have got is

585
00:47:00.530 --> 00:47:05.630
145. If we want to go further to 97% confidence

586
00:47:05.630 --> 00:47:10.830
interval, sample size will be 177 or 99% confidence interval,

587
00:47:10.930 --> 00:47:16.330
sample size will be 250. So these way we can just calculate

588
00:47:16.330 --> 00:47:22.230
sample size for various research. For example, if you want to conduct

589
00:47:22.230 --> 00:47:26.630
a study for prevalence of anemia in pregnancy or any topic of

590
00:47:26.730 --> 00:47:31.830
anemia in pregnancy, we just search for research articles

591
00:47:31.930 --> 00:47:36.330
in Google Scholar. What is the prevalence of anemia in pregnancy? So

592
00:47:36.830 --> 00:47:42.430
we will just try to open if the prevalence is mentioned anywhere

593
00:47:42.830 --> 00:47:47.030
and we need to find out a number which quotes the prevalence

594
00:47:47.130 --> 00:47:51.230
that this much is the prevalence of anemia in the pregnancy. So

595
00:47:51.230 --> 00:47:55.230
here they have got overall prevalence of anemia in the pregnant woman

596
00:47:55.230 --> 00:48:00.730
of 36.8%, okay? Which is around 38%, 37%,

597
00:48:00.730 --> 00:48:06.030
sorry. So we can code this study by Muhammad

598
00:48:06.030 --> 00:48:09.530
Karami at all. So this is M Karami at all. If we

599
00:48:09.530 --> 00:48:14.030
want to cite this article, you can just click on cite and

600
00:48:14.030 --> 00:48:18.830
you can just copy the Vancouver style citations from here and you

601
00:48:18.830 --> 00:48:23.030
can just a control c or copy it and you can copy

602
00:48:23.930 --> 00:48:28.430
and paste it to your references. So M Karami at all says

603
00:48:28.430 --> 00:48:34.230
that the global prevalence of the anemia in pregnancy it is 37%.

604
00:48:34.530 --> 00:48:39.430
Now we want to calculate sample size for prevalence of anemia and

605
00:48:39.430 --> 00:48:44.030
pregnancy. We will go to the open API menu, sample size, proportion.

606
00:48:44.130 --> 00:48:48.430
In the proportion, we will go to enter new data. Anticipated frequency

607
00:48:48.430 --> 00:48:54.030
is 37%, confidence interval, confidence limit or absolute precision is 5%

608
00:48:54.330 --> 00:48:59.130
and we will just hit calculate. For 95% confidence interval, we need

609
00:48:59.130 --> 00:49:04.230
to include 359 cases of anemia, okay?

610
00:49:04.330 --> 00:49:08.330
So this is how the sample size will be calculated for various

611
00:49:08.330 --> 00:49:13.030
studies and if you have any questions or if you want me

612
00:49:13.030 --> 00:49:19.430
to guide you regarding sample size calculation, yes. So

613
00:49:21.830 --> 00:49:26.030
what is the impact of anticipated attrition rate on sample size? Yes.

614
00:49:26.030 --> 00:49:30.130
So this is a very good question by an attendee. So the

615
00:49:30.130 --> 00:49:35.630
for anticipated attrition rate, you can just include 10%

616
00:49:35.630 --> 00:49:40.730
more samples in your study. Say for example, in this particular sample

617
00:49:40.730 --> 00:49:44.830
size for this particular study, we got sample size of 359. You

618
00:49:44.830 --> 00:49:48.430
just add one line to compensate for the attrition rate or to

619
00:49:48.430 --> 00:49:52.830
compensate for the loss of data, loss of follow-up. We will include

620
00:49:52.830 --> 00:49:58.030
10% more cases. That will be 359 plus 10% will be around

621
00:49:58.030 --> 00:50:02.200
36 cases and that will be total around 400 cases. So for

622
00:50:02.200 --> 00:50:07.400
this particular study you can include 10% more cases

623
00:50:07.400 --> 00:50:11.900
and you can justify the sample size modified sample size as 400

624
00:50:11.900 --> 00:50:17.100
total number of cases. So that's all regarding different sampling techniques

625
00:50:17.100 --> 00:50:22.200
and the sample size calculation hands-on training. I again

626
00:50:22.500 --> 00:50:27.800
thank you very much assimilate by meta university and Dr. madam for

627
00:50:28.100 --> 00:50:32.700
conducting and for organizing this research. So thank you so much Dr.

628
00:50:32.700 --> 00:50:35.800
Superna ma'am and thank you so much all the participants for the

629
00:50:35.800 --> 00:50:38.100
questions and for patient listening.
