ID: 56621
Added: 2004-03-03 13:10
Modified: 2004-11-03 9:58
Refreshed: 2012-02-10 18:32
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| Module 12: PLAN FOR DATA COLLECTION |

Document(s) 18 of 27

NB: Development of a research process is a cyclical process. The double-headed arrows indicate that the process is never linear. Module 12: PLAN FOR DATA COLLECTIONOBJECTIVES At the end of this session, you should be able to: - Identify and discuss the most important points to be considered when starting to plan for data collection.
- Determine what resources are available and needed to carry out your study.
- Describe typical problems that may arise during data collection and how they may be solved.
- Prepare a plan for data collection for the research proposal you are developing.
- Introduction
- Stages in the data collection process
I. INTRODUCTIONWhere are we now in the development of our research proposal?Look again at the flowchart in Module 7 that introduces research design. We have just finished four crucial theoretical sessions, in which we have defined: - what information we want to collect to answer the research questions implied by our objectives (Module 8: Variables)
- what approach we will follow to collect this information (Module 9: Study types)
- what techniques and tools we will use to collect it (Module l0: Data collection techniques)
- where we want to collect the data, how we will select our sample and how many subjects we will include in our study (Module 11: Sampling)
Now we enter a new phase in the development of our research methodology: planning our fieldwork. We have to plan concretely how we will collect the data we need (Modules 12 and 1 5), how we will analyse it (Module 13), and how we can test the most crucial parts of our methodology (Module 14). Finally, we will have to develop a work plan to budget the resources necessary to carry out the study (Module 16). A PLAN FOR DATA COLLECTION can be made in two steps: - Listing the tasks that have to be carried out and who should be involved, making a rough estimate of the time needed for the different parts of the study, and identifying the most appropriate period in which to carry out the research (the present module).
- Actually scheduling the different activities that have to be carried out each week in a work plan (Module 15).
Before the proposal development workshop is finished, a pre-test of the data collection and data analysis procedures should be made. The advantages of conducting a pre-test before we finalise our proposal is that we can draft the work plan and budget based on more realistic estimates, as well as revise the data collection tools before we submit the proposal for approval. However, further pre-testing and planning of the research have to be done in the field (Module 14). Why should you develop a plan for data collection?A plan for data collection should be developed so that: - you will have a clear overview of what tasks have to be carried out, who should perform them, and the duration of these tasks;
- you can organise both human and material resources for data collection in the most efficient way; and
- you can minimise errors and delays which may result from lack of planning (for example, the population not being available or data forms being misplaced).
It is likely that while developing a plan for data collection you will identify problems (such as limited manpower), which will require modification of the proposal. Such modifications might include adjustment of the sample size or extension of the period for data collection. II. STAGES IN THE DATA COLLECTION PROCESSWhat are the main stages in the data collection process?Three main stages can be distinguished: Stage 1: Permission to proceed Stage 2: Data collection Stage 3: Data handling Stage 1: PERMISSION TO PROCEEDConsent must be obtained from the relevant authorities, individuals and the community in which the project is to be carried out. This may involve organising meetings at national or provincial level, at district and at village level. For clinical studies this may also involve obtaining written informed consent. Most likely the principal investigator will be responsible for obtaining permission to proceed at the various levels. The Health Research Unit in the Ministry of Health or the institution organising the course may assist in obtaining permission from the national level. Note: In many countries research proposals have to be screened for scientific and ethical integrity by national research councils. However, proposals developed during workshops may be exempted from this procedure if the research is considered as a training exercise and the research council is assured that the course facilitators and Health Research Unit have screened the methodology during the workshop. Stage 2: DATA COLLECTIONWhen collecting our data, we have to consider: - Logistics: who will collect what, when and with what resources
- Quality control
1. Logistics of data collectionWHO will collect WHAT data? When allocating tasks for data collection, it is recommended that you first list them. Then you may identify who could best implement each of the tasks. If it is clear beforehand that your research team will not be able to carry out the entire study by itself, you might plan to look for research assistants to assist in relatively simple but time-consuming tasks. For example, in a study into the effects of improvements in delivery care on utilisation of these services the following task division could be proposed:

HOW LONG will it take to collect the data for each component of the study?Step 1: Consider: - The time required to reach the study area(s);
- The time required to locate the study units (persons, groups, records); If you have to search for specific informants (e.g., users or defaulters of a specific service) it might take more time to locate informants than to interview them.)
- The number of visits required per study unit. For some studies it may be necessary to visit informants a number of times, for example if the information needed is sensitive and can only be collected after informants are comfortable with the investigator or if observations have to be made more than once (for example, follow-up of pregnant mothers or malnourished children). Time needed for follow-up of non-respondents should also be considered.
Step 2: Calculate the number of interviews that can be carried out per person per day (e.g., 4) Step 3: Calculate the number of days needed to carry out the interviews. For example: - you need to do 200 interviews,
- your research team of 5 people can do 5 x 4 = 20 interviews per day,
- you will need 200:20 = 10 days for the interviews.
Step 4: Calculate the time needed for the other parts of the study, (for example, 10 days) Step 5: Determine how much time you can devote to the study. Since the research team usually consists of very busy people, it is unlikely that team members can spend more than 30 working days on the entire study: - 5 days for preparation (including pre-testing and finalising questionnaires),
- 20 days actual field work,
- 5 days data processing + preliminary analysis.
If the team has 20 days for fieldwork, as in the example above, it could do the study without extra assistance. However, if the research team has only five days available for the interviews, they would need an additional five research assistants to help complete this part of the study.
Note: The recruitment of research assistants for data collection may, on the one hand, relieve the research team, but, on the other hand, the training and supervision of research assistants require time (see Annex 12.1). The team has to carefully weigh advantages and disadvantages. If none of the team members has previous research experience, they might prefer designing a study, which they can carry out themselves, without or with only minimal assistance. If research assistants are required, consider to what extent local health workers can be used. They have the advantage of knowing the local situation. They should never be involved, however, in conducting interviews to evaluate the performance of their own health facility. Local staff from related services (teachers, community development) or students might help out. Sometimes village health workers or community members can collect certain parts of the data.
Note: It is always advisable to slightly overestimate the period needed for data collection to allow for unforeseen delays. In WHAT SEQUENCE should data be collected?In general, it is advisable to start with analysis of data that is already available. This is essential if the sample of respondents is to be selected from the records. Another rule of thumb is that qualitative research techniques (such as key informant interviews, focus group discussions) that are devised to focus the content of questionnaires for interviewing larger groups of informants should be carried out before finalisation of these questionnaires. FGDs designed to provide feedback on issues raised in larger surveys, should, logically, be conducted after preliminary analysis of the questionnaires. To use time and transport efficiently, data to be drawn from different sources but in one locality should be collected at the same time. (For example, interviews with health staff in a Health Centre, observations of equipment available in the Health Centre and interviews with mothers living around the Health Centre should be scheduled together.) WHEN should the data be collected?The type of data to be collected and the demands of the project will determine the actual time needed for the data to be collected. Consideration should be given to: - availability of research team members and research assistants,
- the appropriate season(s) to conduct the field work (if the problem is season-related or if data collection would be difficult during certain periods),
- accessibility and availability of the sampled population, and
- public holidays and vacation periods.
Note: The field visit to obtain consent from local authorities for the research may also be used to obtain necessary details about the best period for data collection and availability of local resources (research assistants, transport), if required. 2. Ensuring qualityIt is extremely important that the data we collect are of good quality, that is, reliable and valid. Otherwise we will come up with false or misleading conclusions. In the previous modules possible sources of data distortion (bias) have been discussed which we should try to prevent. They include: - Deviations from the sampling procedures set out in the proposal.
- Variability or bias in observations or measurements made because:
— Our study subject changes his/her behaviour as a consequence of the research. For example, a subject may act more positively while being observed; blood pressure and pulse may increase when the subject is apprehensive. — We use unstandardised measuring instruments. For example, we may use unstandardised weighing scales or imprecise or no guidelines for interviewing. — Researchers themselves vary in what they observe or measure (observer variability). For example, researchers may be selective in their observations (observer bias); measure, question or note down answers with varying accuracy or follow different approaches (one being more open, friendly, probing than the other). - Variations in criteria for measurement or for categorising answers because we changed them during the study.
There are a number of possible measures that can be taken to prevent and to partly correct such distortions. Remember: prevention is FAR better than cure!! Cure is usually surgery: you may have to cut out the bad parts of your data or, at best, devise crutches. Measures to help ensure good quality of data: - Prepare a field work manual for the research team as a whole, including:
— Guidelines on sampling procedures and what to do if respondents are not available or refuse to co-operate.(See Module 11, section II-3), — A clear explanation of the purpose and procedures of the study which should be used to introduce each interview, and — Instruction sheets on how to ask certain questions and how to record the answers. - Select your research assistants, if required, with care. Choose assistants that are:
— from the same educational level; — knowledgeable concerning the topic and local conditions; — not the object of study themselves; and — not biased concerning the topic (for example, health staff are usually not the best possible interviewers for a study on alternative health practices). - Train research assistants carefully in all topics covered in the field work manual as well as in interview techniques (see Annex 12.1 and Module 10B part V) and make sure that all members of the research team master interview techniques such as:
— asking questions in a neutral manner; — not showing by words or expression what answers one expects; — not showing agreement, disagreement or surprise; and — recording the answers precisely as they are provided, without sifting or interpreting them. - Pre-test research instruments and research procedures with the whole research team, including research assistants (see Module 14).
- Take care that research assistants are not placed under too much stress (requiring too many interviews a day; paying per interview instead of per day).
- Arrange for on-going supervision of research assistants. If, in case of a larger survey, special supervisors have to be appointed, guidelines should be developed for supervisory tasks.
- Devise methods to assure the quality of data collected by all members of the research team. For example, quality can be assured by:
— requiring interviewers to check whether the questionnaire is filled in completely before finishing each interview; — asking the supervisor to check at the end of each day during the data collection period whether the questionnaires are filled in completely and whether the recorded information makes sense; and — having the researchers review the data during the data analysis stage to check whether data are complete and consistent.
Stage 3: DATA HANDLINGOnce the data have been collected and checked for completeness and accuracy, a clear procedure should be developed for handling and storing them: At some stage questionnaires and other research tools will have to be numbered. Decide if this should be done at the time of the interview or at the time the questionnaires are stored. Usually each tool used will get its own numbers starting from 1. However, if some data sets are linked, e.g., you interview leprosy patients as well as their relatives and neighbours to analyse their interaction and possible stigma from different perspectives, you better link the numbers. For example, if you have interviewed a patient, P9, his neighbour will be N9 and his wife or son/daughter will be R9. Identify the person responsible for storing data and the place where it will be stored. Decide how data should be stored. Record forms should be kept in the sequence in which they have been numbered.
GROUP WORK (1¾ hours) Make a plan for data collection, considering the points below: - Permission to proceed (10 minutes)
- Which organisations or individuals should be approached to obtain permission to proceed with the research project?
- Who will ask for permission? When? What procedures will be followed?
- Data Collection (1-¼ hours)
- List the different components of your study and the number of interviews, observations or measurements required.
- Calculate for each component how many interviews or observations one person can do per day.
- Decide if you need extra assistance, considering the fact that you, as a research team, will probably not be able to spend more than approximately 20 working days per person in the field and 5 days per person for preparation of the fieldwork.
- If you need research assistants: For which components of the research? How many research assistants? Who would be the right persons to assist you and for how many days will you need them?
- How will you train them? (place, timing, content, duration, trainers)
- How will you ensure their supervision?
- How will the quality of the data be checked and by whom?
- Data handling (5 minutes)
- How will the questionnaires/checklists be numbered?
- How will the data be stored and who has the final responsibility for storing the data?
- Ethical considerations (15 minutes)
Take care that your data collection process is ethical in all respects: - How have you planned to obtain informed consent from your informants? Are there any categories of informants that need special consideration (e.g., children, sick persons, mentally disabled individuals)?
- Are certain parts of the research focused on sensitive issues? How will you handle problems that may arise?
- Do certain parts of your research require extra attention to assure confidentially? How will you handle the issue?
- Summarise the outcome of your group work on a flip chart. Record the details of your discussions so that you can use them for the development of your work plan (Module 15).
Annex 12.1: Training research assistants (as well as other research team members with little research experience)1. Interviewers’ tasksDuring the fieldwork interviewers (or research assistants) may work independently or together with one of the researchers. If they go out independently they may have to carry out the following tasks: - Do the sampling in the field (for example sampling of households within a village and/or sampling of individuals to be interviewed within households).
- Give a clear introduction to the interviewee concerning the purpose and procedures of the interview and ask for permission to interview. (An introductory sheet should be prepared and attached to interview guide or questionnaire, so that each research team member approaches the informants in a similar way.)
- Perform the interviews. Usually it is best to give research assistants more or less structured questionnaires to administer with clear instructions for open questions. It is not wise to assign the more difficult tasks of performing highly flexible interviews or focus group discussions to research assistants unless they are mature, experienced persons.
It is imperative that the researchers train their research assistants so they can carry out their tasks accurately and correctly, according to the procedures developed by the researchers. Research assistants should not be left to develop their own procedures; otherwise bias will be almost certain to result. The training of the research team may take 2 to 3 days. The first day may be devoted to theory, followed by 1 or 2 days of practical training, depending on the local circumstances and the nature of the study. 2. Theoretical trainingResearch assistants must be thoroughly familiar with the objectives of the research project and the methodology. Therefore, it is recommended that they be provided with copies of the research protocol and that the most relevant sections be discussed thoroughly, including: - statement of the problem,
- objectives,
- data collection tools to be used (an overview),
- sampling procedures (if sampling has to be done in the field),
- plan for data collection, and
- plan for data analysis.
It is important at this stage that the research assistants get an ample opportunity to ask questions. Then a more in-depth discussion should follow concerning the data collection tools (interview FGD guides, questionnaires and possibly checklists) that are to be used by the research-team members. For each and every question all should know WHY the information is required. Research assistants should be taught basic interview techniques, such as - asking questions in a neutral manner;
- not showing by words or expression what answers one expects;
- not showing agreement, disagreement or surprise; and
- recording answers to open questions precisely as they are provided, without sifting or interpreting them.
Clear instructions should be given as well, concerning to what extent an interviewer is allowed to alter the phrasing of questions, if it seems necessary, and whether he/she should probe for answers. For questions which have pre-categorised answers it should be made clear whether the possible answers should be mentioned by the interviewer during the interview or not. (Usually they are not to be mentioned.) There should be no misunderstandings concerning how to record answers and observations. Finally, explanations should be given concerning how an interviewer should introduce him or herself to the interviewee, what to say concerning the purpose of the study, how to ask for consent, and how to close the interview. 3. Practical trainingPractical training in interviewing is essential. This may be provided in two stages. (See Module 10B part V, interview exercise.) Firstly, role-plays can be performed, during which one trainee assumes the role of the interviewer and another plays the interviewee. Other trainees and the trainers (researchers) should observe carefully what happens and give constructive feedback right after the role-play. Then roles can be changed, until each trainee has had a chance to practice each type of interview at least once. Secondly, a field test should be conducted, which will serve two purposes: the training of the entire research team including research assistants, and a (further) test of the data collection tools. A test of the tools is essential if a previous field-test resulted in important changes and/or if the questionnaire(s) were translated into a local language after the first field test. If the research assistants will be involved in the proper phrasing of questions this will definitely strengthen their interest and commitment. The field test is best carried out in groups of 2 to 3 persons (see Module 14), with each team including at least one trainer and one trainee. Note that after the field test constructive critique of each interview should be made, starting from the moment the interviewee was approached up to the farewell. 4. Supervision of research assistantsEven if research assistants are used, responsibility for the research remains with the research team as a whole. To guarantee the quality of the data collected it is important to supervise the research assistants’ performance, especially at the beginning of the data collection period. If they are going out into the field independently, plans could be made to accompany them on selected visits and/or to question a small sample of the interviewees as a ‘control group’ concerning key aspects of the interview. As a further quality control check it is important that an interviewer’s name (or interviewer’s code) appears standard on each questionnaire/checklist so that it is possible to ask for clarification if certain information is not clear. Trainer’s NotesModule 12: PLAN FOR DATA COLLECTIONTiming and teaching methods | ¾ hour | Introduction and discussion | | 1¾ hours | Group work | | 1 hour | Plenary | | 3½ hours | TOTAL TIME |
Introduction and discussion- Explain that we are entering a new phase in the development of the methodology, in which we go from theory to practice: the concrete planning of the data collection process.
- Of the three phases that can be distinguished in the planning for data collection (i.e., permission to proceed, actual data collection and data handling), planning for actual data collection will require most attention, both in the presentation and in the group work.
- The logistics of data collection is one major aspect of the planning: WHO will collect WHAT and WHEN. It is important that relatively inexperienced researchers give thought to this aspect of data collection before the pre-test, so that they can consciously check whether their plans are realistic.
- As the participants begin planning for data collection they should clearly distinguish and list the different components of their study. Next, they should consider the time it will take to carry out the different components, so that they can decide whether they can do the study alone or whether they need assistance.
- Take the most labour-intensive part of one of the studies being developed in the workshop and follow the steps outlined in the module to determine the time needed.
- If you do not want to favour one of the groups, you can use the example of the utilisation of delivery care provided in the module or any other example that resembles the topics participants are working on.
- Discuss the advantages and disadvantages of using research assistants and of using local health service personnel as research assistants.
- Then proceed to the second major aspect of the planning for data collection, that of ensuring quality.
- Stress the importance of preparing a fieldwork manual (irrespective of whether research assistants are recruited or not) and of using appropriate interview techniques. Refer to Annex 12.1 for more detailed guidelines on how to train interviewers.
Group work- Make sure that participants have understood the principle of calculating the time required for each component of the study and that they calculate carefully the time needed for the most labour-intensive parts of the study, so that they can decide:
— whether they need assistance, and — who would be appropriate research assistants, if required. - Let them summarise ethical issues involved in data collection, which have been discussed during previous presentations. Participants need to include a section on ethical considerations in their research proposal (see Module 18 or Module 1 for content of the research proposal).

Document(s) 18 of 27
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