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HOW TO DO A STUDY

BY DUNCAN SAUNDERS

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59,

INTRODUCTION.

In the first article in CRITICAL HEALTH, Number 2, on the use of epidemiology in South Africa, which appeared the following was discussed :-

(i) The scope of epidemiology;

(ii) Some issues relating to the decision to do a particular study;

(tit) Examples of ways in which epidemiology can be used (using mainly South African studies).

This article is intended as an introduction for people who may want to do a study but feel uncertain of how to go about doing

it. The techniques described may be used for studies of many things that ere not necessarily medical but may be

health-related. Examples d.re studies of housing conditions or of level of literacy in a community,

The first section outlines the stages common to all types of studies. The second section deals with some of the

methodological issues to be considered when doing a descrip- tive study.

Stages of a Study:

Table 1 shows the stages of a study as listed by Abramson.

Each stage is dependant on the preceding one.

1. Preliminary Steps:

The first steps in converting an interest in doing a study into a concrete proposal are taken by answering the follow ing questions ?

(i) What is the purpose of the study ? (ii) What aspect of a health problem am I

going to investigate ?

Hypertension (high blood pressure) may be a common problem in the area in which one is working.

A number of different kinds of study may usefully be done e.g.

(i) Studies of the prevalence of hypertension in the area,

(ii) Studies looking at factors associated with hyper- tension,

(iii) Studies looking at interventions aimed at reducing

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STAGES OF A STUDY.

1. Preliminary Steps

2. Planning.

3. Preparing for data collection.

4. Collecting the data.

5. Processing and analysing the data.

6. Writing a Report.

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61.

hypertension. This type of study may also be useful to decide on what sorts of health care services are needed to deal with the problem.

In addition one may have different reasons for doing any particular kind of study. A prevalence study may be done to help estimate the size of the problem so that appropri- ate interventions may be planned. Alternatively, the

purpose may be to monitor the effect of rapid urbanization on blood pressure. The purpose of the study has impli- cations for the planning of the study such as the choice of population to be studied and the sample size required.

Having decided what one is going to investigate, and why, planning of the study can begin.

Planning the Study:

The value of a study depends on careful planning. This stage may take longer than any of the other stages or all the other stages combined. Some of the issues to be

considered in planning a descriptive study will be discus- sed in the second part of this article. By the end of this stage one should have a written protocol (outline) which describes what information is needed and how it is

to be collected and analysed.

Preparing for data collection:

Having finalised a plan for a study one needs to test the methods used and to make various practical arrangements.

Pretesting of methods is always necessary. Sometimes all that is required is to look at a few clinic cards to see whether certain information is routinely collected. At

other times a pilot study or "dress rehearsal" needs to be done. The pilot study should be done in exactly the same

way as you are planning to do the main study. In this

way you can pick up problems with your study (e.g. questions that are not phrased clearly) before you actually start the study itself. At times one is testing to see whether any unforeseen difficulties crop up. Time after time major flaws are detected in apparently well constructed question- naires. At other times one is looking for particular

information. Many studies are inconclusive because sample are too small. A pilot study can help onedecide on the

size of the sample needed to answer the question one is asking.

Practical arrangements for the main study may need to be

made at this stage, including :-

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( i i i ) Obtaining equipment and p r i n t i n g q u e s t i o n n a i r e s . ( i v ) Obtaining informed consent and co-operation from

p a r t i c i p a n t s . 4. C o l l e c t i n g the Data:

A f t e r the s t i m u l a t i o n of planning the study comes the often r a t h e r d u l l period of c o l l e c t i n g the data i n a systematic manner. At t h i s stage one needs to monitor two aspects of

the study.

( i ) A record should be kept of p a r t i c i p a n t s and non- p a r t i c i p a n t s ( i . e . those who do not answer the q u e s t i o n n a i r e ) . For example people who do not

p a r t i c i p a t e ( r e p l y ) i n a questionnaire on l e v e l of l i t e r a c y may i n f a c t be i l l i t e r a t e . I n t h i s way one can a c t e i t h e r t o o b t a i n improved p a r t i c i p a t i o n i n the study or one can c o l l e c t i n f o r m a t i o n to

enable one t o assess the sample bias caused by the n o n - p a r t i c i p a t i o n .

( i i ) The q u a l i t y of the data being c o l l e c t e d should be checked.

5. Processing and I n t e r p r e t i n g the Data:

Processing the data involves f i r s t l y , l o o k i n g at the data

f o r possible e r r o r s of recording and i n d e x i n g . Following t h i s the data are arranged i n the format one needs t o

i n t e r p r e t i t . During the planning stage i t is useful t o construct dummy tables of the data to be c o l l e c t e d . At a n a l y s i s stage one then f i l l s i n the data obtained from the survey i n these t a b l e s . I n t e r p r e t i n g the data involves making sense of them and deciding what the p r a c t i c a l i m p l i -

cations a r e .

6. W r i t i n g a Report:

Even i f the r e s u l t s are only o f i n t e r e s t t o the i n v e s t i g a - t o r , no study i s complete u n t i l a r e p o r t has been w r i t t e n . PART TWO.

Planning a Descriptive Study:

A descriptive study is designed to find out the size of a

health problem. The design of descriptive studies is rela-

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'its NoT

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y i e l d , i . e . the o b j e c t i v e of the study. This can u s e f u l l y be \ set out in the form of a question w i t h the f o l l o w i n g c h a r a c t e r i s e

t i c s . ' 1. I t can be answered by a number.

2. Each term i n the question i s c l e a r l y d e f i n e d .

e . g . What is the prevalence of hypertension i n population Y at time X ?

The main issues involved i n the design of a study to answer such

a question are shown i n f i g u r e 1 . ]

1. The Study Population:

The choice of study population is often i m p l i c i t i n the ? purpose of the study. How generalizable one wants the

study to be is important i n d e f i n i n g a study population.

I t is inappropriate to use c l i n i c attenders to measure the prevalence of hypertension in the surrounding area. How- ever, t h i s population would be appropriate i f one was

interested i n the hypertension prevalence of c l i n i c attenders.

I f one wanted to measure the prevalence of hypertension i n a p a r t i c u l a r community, one would have to randomly study members of the community and not only those attending the

c l i n i c .

Sample Selection:

To measure the blood pressure of every person i n a large

c i t y is a d i f f i c u l t t a s k . The e f f o r t and expense involved i n measuring the prevalence of hypertension can be reduced by sampling. However, the disadvantage of sampling i s that one can only estimate the size of the health problem.

By using c e r t a i n sampling methods one can make a statement about the prevalence c f hypertension in the whole population w i t h measurable confidence and p r e c i s i o n . I f one measured

the blocd pressures on the v/hcle population one could say t h a t the prevalence of hypertension i n the population was e . g . 2U7-. However, i f a random sample of people from t h i s

population had blood p r ^ s u r e s taken QTI£ would only be able to sa> e . g . t h a t on? is 95? confident t h a t tho prevalence of hypertension is between \T% and 23<.'>.

I t i s important t o seek s t a t i s t i c a l advice about the sample size required f o r a p a r t i c u l a r study. At t h i s stage one

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FIGURE 1

DESCRIPTIVE STUDY DESIGN.

; A J ;

DESIGN: ISSUES

Study Population

Defined ?

Generalizable Size

Sample Random ?

Size ?

Measurements

Valid ?

Repeatable ?

Response Rate

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ned. The purpose of this study was to estimate the number of tuberculosis sufferers in the community not known to the T.B. service. However, if positive sputum tests were found at a rate of 7/1000 in the sample one could be

95% confident that the population prevalence rate was

between 4/1000 and 11/1000. This estimate was too impre- . cise to be of help and therefore other methods were

developed to find out how adequately the T.B. service was finding tuberculosis sufferers.

3. Measurements:

To be u s e f u l , measurements should be v a l i d and repeatable.

V a l i d i t y i s the extent t o which the measurements r e f l e c t what one i s t r y i n g t o measure. With regard t o blood

pressure the question i s : - does an i n d i r e c t blood

pressure reading (sphygnomanometer reading) r e f l e c t the i n t r a - a r t e r i a l pressure ?

R e a l i a b i l i t y i s the extent t o which s i m i l a r i n f o r m a t i o n i s obtained by repeated measurements. Blood pressure readings on one person may vary e i t h e r because of v a r i a t i o n s i n the blood pressure, the instrument or the observers. Reada- b i l i t y can be enhanced i n t h i s instance by adapting a

standard procedure f o r t a k i n g the blood pressure, regular checking of the sphygnomanometers (blood pressure meters) used and t r a i n i n g the observers r e s p e c t i v e l y .

4 . Response Rate:

As non respondents are often d i f f e r e n t from respondents i t i s important t h a t a high response rate i s o b t a i n e d . As a r u l e a 80% response r a t e i s acceptable. I f the response r a t e i s lower than t h i s one should i n v e s t i g a t e whether the non-respondents are l i k e l y t o be d i f f e r e n t to

the respondents f o r the v a r i a b l e being s t u d i e d . CONCLUSION:

The i n t e n t i o n of t h i s a r t i c l e was t o serve as an i n t r o d u c t i o n , f o r people who were uncertain how t o go about doing a study.

The books by Abramson and Barker are h i g h l y recommended f o r those who would l i k e t o learn more about t h i s .

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57 In p a r t i c u l a r Abramson deals thoroughly w i t h a l l aspects of study design and i l l u s t r a t e s points made w i t h numerous

examples and references.

R E F E R E N C E S :

1. Abramson, G.H. (1979)

Survey Methods in Community Medicine.

An introduction to Epidemiological and Evaluative Studies Churchill Livingstone, Edinburgh, 2nd Ed.

2. Barker, P.G.P. (1976).

Practical Epidemiology.

Churchill Livingstone, Edinburgh, 2nd Ed.

NOTE:

People i n t e r e s t e d i n doing a study on issues of concern to communities and who r e q u i r e f u r t h e r advice on how t o do i t

are welcome to send t h e i r queries t o C r i t i c a l Health and the editors w i l l put them i n t o contact w i t h resource people t h a t _wiIL_b£_ahle_ t o a s s i s t them.

% > * . ' - • A * "SkiJEifl-.V-J

HEALTH CARE

aon P I 1980

Gastroenteritis:

prevention and cure

Available froe from:Health Care 17 Main Road

Mowbray, Cape Town

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