Data Acquisition Approach ll Flashcards

1
Q

Primary data collection method (3)

A
  1. Experimental method
    - lab experiment
    - controlled trials
  2. Observation method
  3. Survey method
    - in-depth interview
    - focus group discussion
    - questionnaire
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2
Q

Issues regarding questionnaire constructions (5)

A
  1. Structural
  2. Content
  3. Language
  4. Pre-testing
  5. Reliability & validity
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3
Q

Steps in constructing questionnaire (4)

A
  1. Determine what information is needed
  2. Drafting of questions
  3. Pre-testing of questionnaire
  4. Revision of questionnaire, if needed
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4
Q

Structural issues (2)

A
  • mode of delivery of questionnaire

- open-ended or close-ended

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5
Q

General format

A
  1. Introductory statement
  2. Demographics questions
    - can be last section also
  3. Factual questions
  4. Opinion questions
  5. Closing statements & return instructions
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6
Q

Question context (2)

  • administration
  • delivery of questionnaire
A
  1. Administration of questionnaires
    - self administered
    - interviewer-administered
  2. Delivery of questionnaire
    - mails / emails
    - telephone
    - in person
  • determines how questions & response options are constructed
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7
Q

Types of question formats (2)

A
  1. Open-ended
  2. Close-ended
    - checklists
    - rankings
    - rating scales
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8
Q

Examples of rating scales (5)

A
  • Unipolar scale
  • Bipolar scale
  • Likert scale
  • Visual Analogue Scale (VAS)
  • Wong-Baker face scale
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9
Q

Advantages of open-ended response (4)

A
  • more detailed answers
  • can study respondents’ interpretations expressed in their own words
  • minimise successful guessing (knowledge question)
  • useful to wrap up entire survey at the end
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10
Q

Disadvantages of open-ended response (7)

A
  1. Less structured
  2. Difficult to ensure systematic recording of response (if interviewer administered)
  3. Difficult to maintain unbiased while adequately probe for more complete/understandable answer
  4. More difficult for respondents to answer compared to close-ended response
  5. More time required to complete such question
  6. ~75% of respondents will leave such questions blank (if self-administered)
  7. Difficult to code information for data analysis
    - wider variety of response
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11
Q

Advantages of close-ended response (4)

A
  1. Tightly structured
    - only options for respondents to choose from
  2. Ensures standardisation of response
  3. Easily encoded & analysed
  4. Less time taken to collect response
    - respondents take a shorter time to answer
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12
Q

Disadvantages of close-ended response (4)

A
  1. Less depth in answers
  2. Imposes researchers priorities on respondent
  3. May bias responses if range of options are not exhaustive
  4. Presentation formats may affect responses
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13
Q

How to write good questions? (4)

A
  • be clear
  • be concise
  • provide complete options in close-ended questions (avoid gaps or overlap categories)
  • bias & leading questions
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14
Q

Clarity in questions by avoiding __ (4)

A
  • big words
  • technical jargons (use layman terms)
  • double negatives
  • double-barreled questions
    eg questions with or, and
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15
Q

Language issues (3)

A
  • translate to other languages
  • cross cultural adaptation of survey instrument (translate to appropriate language)
  • back translate to ensure meaning of questions is retained
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16
Q

Pre-testing (4)

A
  • pilot test with a group of respondents
  • ensure all questions are understood as intended, otherwise rephrase to capture intended meaning
  • check length of questionnaire
  • ensure questionnaire is able to obtain adequate information to answer research question
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17
Q

Strengths of self-administered questionnaire (3)

A
  1. Cheap to administer
  2. Less susceptible to interviewer bias
  3. Can be administered via mail / email
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18
Q

Limitations of self-administered questionnaire (3)

A
  1. Lower response rate
    - lead to non-response bias
  2. Difficult to elicit detailed response
  3. Less control over how questionnaire is filled out
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19
Q

Strengths of interviewer-administered questionnaire (3)

A
  1. Higher response rate
  2. More detailed responses can be elicited
  3. Greater control over how questionnaire is filled out
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20
Q

Limitations of interviewer-administered questionnaire (3)

A
  1. Expensive to administer
  2. More susceptible to interviewer bias
  3. More time consuming
    - interviewer has to be present to collect response
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21
Q

Response rate

A

= (no. of participants who completed the questionnaire)/(total no. of eligible persons who were asked to participate)

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22
Q

Concerns over low response rate (3)

A
  • leads to non-response bias as respondents may differ from non-respondents in their characteristics, hence answers of respondents may differ from the potential answer of non-respondents
  • compromise internal validity
  • weakens external validity & generalisability of survey results
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23
Q

When to use mail/email mode of delivery of questionnaire? (6)

A
  1. Geographically disperse sample groups
  2. Directed to specific groups
    - can obtain specific emails
  3. Limited research budget & manpower
  4. Provide time for respondents to think before answering
  5. Provide privacy for respondents
  6. Questions should be closed-ended, simple & clear
24
Q

When to use telephone interviews? (2)

A
  1. Open-ended questionnaire
  2. Complex interviews
    eg req skipping of questions depending on respondent’s previous answer
25
CATI
Computer Assisted Telephone Interviews - directly key in respondent's answers into computer system - ensure quality & speed
26
When to use in-person interviews? (3)
1. Open-ended questionnaire 2. Complex interviews eg req skipping of questions depending on respondent's previous answer 3. Knowledge-based questions
27
CAPI
Computer Assisted Personal Interviews - directly key in respondent's answers into computer - ensure quality & speed
28
Practicality considerations when using mail/email to delivery questionnaires (3)
1. Accessibility of sample - req specific emails/mailing address 2. Low response rate (5-30%) 3. Think of ways to increase response rate eg incentives, provide return envelope with postage, reminders, deadlines
29
Practicality considerations when using telephone interviews (2)
1. Accessibility of sample - req contact details 2. Good response rate (65-75%)
30
Practicality considerations when using in-persons interviews (2)
1. Accessibility of sample - req locations of sample 2. Good response rate (70-80%)
31
Turn Around Time (TAT)
= (no. of surveys to be collected x duration of each interview) / (no. of interviewers x no. of hours each interviewers works per day)
32
Census
Entire population
33
Sampling
- a subset of the population
34
Sample size calculations for Questionnaires (2)
=/ sample size calculator for clinical trials 1. Cochran's formula - large sample size - small sample size (>5%) 2. Yamane's formula - fixed 95% CI - p=0.5
35
Cochran's formula (large population)
no = [(Z^2)(pq)] / (e^2) no = sample size calculated Z = Z score of normal distribution = 1.96 at 95% CI p = estimated proportion of an attribute that is present in the population = 0.5 (if unknown) q = 1-p e = desired level of precision = 0.05
36
Cochran's formula (small population)
- when no/N > 5% n = no / [1+[(no-1)/N]] ``` n = sample size for small population no = sample size calculated for large population N = population size ```
37
Yamane's formula
- assuming 95% CI and p=0.5 n = N / [1+N(e^2)] n = sample size calculated N = population size e = desired level of precision = 0.05
38
Types of sampling (2)
1. Random / Probability sampling | 2. Non-random / Non-probability sampling
39
Types of Random / Probability sampling methods (4)
1. Simple random sampling 2. Systematic random sampling 3. Stratified random sampling 4. Cluster sampling
40
Types of Non-random / Non-probability sampling (3)
1. Convenience sampling 2. Quota sampling 3. Snow-ball sampling
41
Simple random sampling (2)
- every subject has an equal probability of being selected | - req a full list
42
Systematic random sampling (4)
- req a full list - generate a random number to determine the _th item to select - generate another random number from 1 to _ to determine the starting number - _ is determined by dividing population size by desired sample size
43
Stratified random sampling (2)
- divide population into relevant strata | - random sampling from each strata
44
Cluster sampling (3)
- divide populations into clusters - randomly select a subset of clusters - all units or random sample units within subset of clusters are surveyed
45
Convenience sampling
- select participants whom access is easy
46
Quota sampling
- reserve a certain proportion of participants to particular types of people eg gender
47
Snow-ball sampling (2)
- selected participants nominate others whom they know could be interviewed - good to use if target population is difficult to be identified / accessed eg drug addicts
48
Secondary data sources (6)
1. Prescription/medical & dispensing records 2. Registry data * * 3. Claims databases 4. Cross-sectional survey data 5. Large prospective cohort data 6. Spontaneous reporting / surveillance data
49
Data sources with either exposure data or outcomes data only (2)
- req record linkage eg via IC - combining the information from both data belonging to same individual into one record so that the same person is counted only once
50
Strengths of medical/prescription/dispensing records (7)
1. Clinical data available eg labs 2. Best source for disease outcome 3. Efficient - data already collected, large sample size & long follow up data 4. Prospectively collected data 5. Detailed information on medical records 6. Can study many drugs in relation to many outcomes 7. Can conduct nested case-control studies
51
Limitations of medical/prescription/dispensing records (5)
1. Compliance to medication unknown 2. Non-prescription drugs missed eg OTC & GSL 3. Diagnosis based on codes / texts 4. Incomplete information about habits, past history & other potential confounders 5. Uncertain completeness of data from other physicians & sites of care - incomplete data
52
Types of registry data (2)
1. National Registry of Disease Office (NRDO) - cancer - renal - stroke - acute myocardial infarction - donor care (liver & renal) 2. Drug use registry eg pregnancy registries for anti-epileptic drug use
53
Strengths of registry data (4)
1. Details & systematically collected clinical data 2. Representative of patients / drug users 3. Inexpensive if data already available 4. High reliability of data - periodic audits
54
Limitations of registry data (4)
1. Minimal information on drug use 2. No appropriate control or comparison groups - can use other drug users as a comparison or other disease as a control 3. Expensive if data not readily available & have to create one 4. Missing data
55
Considerations in collecting/using secondary data for use (4)
1. Reliability - data collection process - reproducibility 2. Suitability - can the data collected answer the research question 3. Adequacy of data - completeness of data 4. Ethical considerations of data use - may involve IRB - PDPA - de-identification of data