How to write a study protocol - PowerPoint PPT Presentation

1 / 36
About This Presentation
Title:

How to write a study protocol

Description:

Lay down rules for all partners (quality) Obtain approval of ethical ... Case-control study, risk factors for brucellosis in France. 4. Methods. Data collection ... – PowerPoint PPT presentation

Number of Views:99
Avg rating:3.0/5.0
Slides: 37
Provided by: arnold89
Category:

less

Transcript and Presenter's Notes

Title: How to write a study protocol


1
How to write a study protocol
  • EPIET, Lazareto, Menorca
  • September 2005

2
Study protocol What is it?
  • Describes every step of a study
  • Answer relevant questions
  • public health problem important?
  • study question relevant to problem?
  • objectives consistent with study question?
  • study design achieves objectives?
  • sufficient power?
  • public health impact of the findings?

3
Study protocol Why do it?
  • Check
  • can objectives be achieved?
  • is study feasible?
  • Ensure collect crucial information
  • Lay down rules for all partners (quality)
  • Obtain approval of ethical committee(s)
  • Apply for funds

4
Study protocolHow to start ?
  • Get
  • good examples
  • ideas from similar published studies
  • ideas from colleagues
  • Use a checklist of items to include
  • Obtain requested format (grant application)

5
Protocol outline
  • 1. Presentation (cover page)
  • 2. Background and justification
  • 3. Objectives
  • 4. Methods
  • 5. Ethical considerations
  • 6. Project management
  • 7. Timetable
  • 8. Resources
  • 9. References
  • 10. Appendices

6
1. Presentation
  • Title
  • short, accurate, concise
  • Investigators
  • Main centres
  • Steering committee
  • Summary of the protocol

7
2. Background and justification
  • Statement of problem, study justification
  • importance of subject area
  • magnitude, frequency
  • gaps in existing knowledge
  • principal question(s) to be addressed
  • contribution of results to existing knowledge
  • public health use of results
  • Review relevant literature

8
3. Objectives
  • Should answer the study question
  • S.M.A.R.T.
  • Principal objective
  • Must be achieved
  • Dictates design and methods
  • Secondary objectives
  • Of interest, but not essential

9
3. Objectives example 1
  • Principal objective
  • To determine if sharing a haemodialysis machine
    with an HCV infected patient is a risk factor
    for HCV infection.
  • Secondary objective
  • To identify failures in procedures designed to
    prevent cross-infection via haemodialysis
    machines

10
3. Objectivesexample 2
  • To estimate the current mortality, among the
    Internally Displaced Population present in the
    settlements at the time of the survey,
    in each of the three states of
    Greater Darfur region

11
Hypotheses
  • Translation of the objectives in terms that
    allow statistical testing

12
Hypotheses
  • Translation of the objectives in terms that
    allow statistical testing
  • The incidence of HCV infection
    in haemodialysis
    patients
  • is higher
  • in patients sharing machines
    with HCV infected patients
    than
  • in patients not sharing machines
    with HCV infected patients

13
Hypothesis
  • The current crude mortality rate
    in IDPs in Darfur
    is above 1 death per 10,000 per
    day
  • CMR gt 1/10,000/day

14
Protocol outline
  • 1. Presentation
  • 2. Background and justifications
  • 3. Objectives
  • 4. Methods
  • 5. Ethical considerations
  • 6. Project management
  • 7. Timetable
  • 8. Resources
  • 9. References
  • 10. Appendices

15
4. Methods
  • Procedures to achieve objectives
  • what will be done?
  • how?
  • Information used to judge validity

16
4. Methods
  • Study design
  • cohort, case-control, cross-sectional
  • brief justification
  • Study population
  • definition
  • criteria for inclusion and exclusion
  • mechanisms of recruitment
  • accessibility, follow up, representativeness

17
4. Methods
  • Sampling design
  • frame district, household, persons,
  • method random, cluster, stratified,
  • randomisation procedures
  • replacement procedures (in case of refusal)
  • Sample size
  • sample size, power calculations based on
    principal objective
  • feasibility

18
4. Methods
  • Selection and definition
  • exposures
    risk factors,
    protective factors, confounding factors
  • outcomes
    definition of case and
    the control group
  • Items to be measured
  • scales used
  • e.g smoking ? lung cancer
  • smoking definition, quantification, categories
  • lung cancer case definition, control group
    definition

19
CC study of sporadic cases
of Salmonella Enteritidis infection
  • Exposure
  • consumption of custard slices
  • Case
  • a person living in South-West Wales with
    a laboratory confirmed
    infection due to S.Enteritidis
    in June and July 1991
  • Case finding
  • through Public Health Laboratory weekly
    notifications
  • Control
  • persons living in SW Wales in same neighborhood
    as cases
  • Control finding
  • random selection of people using telephones
    directory

20
MethodsData analysis plan
  • Structured in terms of objectives
  • Hypotheses tested, dummy tables
  • Statistical tests used, adjustment,
    standardisation

21
MethodsData analysis plan
  • Define
  • indicators you will need to reach objectives
  • data you will need to collect
  • Better estimates of sample size
    for analysis of sub groups

22
MethodsData analysis
Dummy table Food specific attack rates of
Salmonella infection in a day care centre,
Paris, May 1999
23
MethodsData analysis
  • Case-control study, risk factors for brucellosis
    in France

24
4. MethodsData collection
  • How
  • interview, observation, record review
  • By whom
  • interviewers selection, training
  • level of supervision
  • Tools
  • questionnaires, recording materials
  • questionnaires self or interviewer administered,
    face to face or telephone interview
  • Procedures for taking samples

25
4. MethodsData handling
  • Coding
  • during data collection, afterwards?
  • by whom?
  • Processing
  • software, hardware
  • entry
  • during the study, afterwards?
  • single entry, double entry?
  • Validation and data cleaning

26
4. MethodsPilot studies, pre-testing
  • No study without test
  • Feasibility of sampling
  • Data collection, measurement methods
  • Questionnaire
  • Describe how to test

27
4. MethodsLimitations
  • Identification of potential sources of biases
  • selection bias
  • information bias
  • How to deal with them
  • possibilities for correcting
  • how they will affect the results

28
Protocol outline
  • 1. Presentation
  • 2. Background and justifications
  • 3. Objectives
  • 4. Methods
  • 5. Ethical considerations
  • 6. Project management
  • 7. Timetable
  • 8. Resources
  • 9. References
  • 10. Appendices

29
5. Ethical considerations
  • Informed consent
  • Confidentiality, record anonymity
  • Data storage and protection
  • Ethical committee

30
6. Project management
  • Participating institutes and persons
  • Responsibilities and tasks of each partner
  • Data ownership

31
7. Timetable
  • Planning/organisation of the study
  • questionnaire design, recruitment, purchases
  • permission
  • obtain funding
  • Pilot study
  • Final study
  • data collection
  • analysis
  • presentation of results and write up

32
8. Resources
  • Extent of this section depends on target audience
  • Specify
  • available sources
  • requested sources
  • Keep budget
  • reasonable
  • detailed
  • well justified

33
9. References
  • Limit number of references to key articles
  • Follow recommended style
  • Vancouver
  • www.library.soton.ac.uk/infoskills/vancouver.shtml

34
10. Appendices
  • Methodological appendices
  • List of definitions
  • Questionnaires
  • Introductory letters to study participants
  • Forms for informed consent
  • ..

35
Common problems
  • Too ambitious too many questions
  • Insufficient attention to literature
  • Poor justification
  • why is it important to answer this question?
  • what impact does it have on public health?
  • Poorly formulated objectives
  • Inappropriate analysis
  • Inadequate description
  • Absence of pilot

36
Study protocoland now.
  • Good Luck !
Write a Comment
User Comments (0)
About PowerShow.com