Principles of Research Writing & Design Educational Series Fundamentals of Study Design Lauren Duke, MA Program Coordinator Meharry-Vanderbilt Alliance.

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Presentation transcript:

Principles of Research Writing & Design Educational Series Fundamentals of Study Design Lauren Duke, MA Program Coordinator Meharry-Vanderbilt Alliance 17 July 2015

Session Outline Research Question Type of Study –Observational –Experimental –Quasi-experimental Study Designs –Cross-sectional Studies –Cohort Studies –Case Control Studies –Randomized Controlled Trial (RCT) –Case-series –Case Report

What do you want to know? Cause and effect? Prevalence? Incidence? –Example: What a child watches on television and violent behavior Is this your first study with this population? Is it feasible? –Money –Time –Rare outcomes –Infrastructure How many participants do you have access to?

What do you want to know? Predictor vs. Outcome variables Violent Behavior Television Program

All Studies ExperimentalObservational Randomized Control Trial Non- randomized AnalyticDescriptive Case series Case reportsCohort Study Cross Sectional Case-Control Study Quasi- experimental

Observational Analytic Study Designs

Cross Sectional Studies Can be used to examine associations between two or more variables Prevalence Population Sample Exposed Developed disease Did not develop disease Not Exposed Developed disease Did not develop disease

Cross Sectional Studies Serial Surveys –Using cross sectional studies in the same population over certain time intervals Population Sample Exposed Developed disease? Not Exposed Developed disease? Sample Exposed Developed disease? Not Exposed Developed disease? Sample Exposed Developed disease? Not exposed Developed disease?

Cohort Studies Prospective and Retrospective Incidence –The proportion who develop a disease or condition over time. Outcome has not yet occurred Identify study subjects Classify treatment status Treatment of interest Good outcome Bad outcome Prospective cohort study begins here Retrospective cohort study begins here

Multiple-Cohort Studies Two or more separate samples of subjects –One group with exposure to a potential risk factor, one without –Levels of exposure Exposure Outcome Control Outcome

DesignAdvantagesDisadvantages Cross-sectional - Short duration - Potential first step for a cohort study or clinical trial - Yields prevalence of multiple predictors and outcomes - Does not establish sequence of events - Not feasible for rare predictors or rare outcomes - Does not yield incidence Cohort Designs All- Sequence of events - Multiple predictors & outcomes - Number of outcomes grow over time - Yields incidence - Often requires large sample sizes - Less feasible for rare outcomes - Attrition Prospective- More control over participant selection & measurements - Avoids bias in measuring predictors - Follow-up can be lengthy - Often expensive Retrospective- Data collection complete - Relatively inexpensive - Less control over participant selection & measurements Multiple cohort- Useful for distinct cohorts with different or rare exposures - Bias and confounding from sampling distinct populations

Case-Control Studies “Working backwards” or Retrospective Effect studied first, Cause second Ex. Infant sleeping position and SIDS

DesignAdvantagesDisadvantages Case-Control - Useful for rare outcomes - Short duration, small sample size - Relatively inexpensive - Bias & confounding from sampling two populations - Limited to one outcome variable - Sequence of events may be unclear - Does not yield prevalence or incidence Case-Control Studies

Observational Descriptive Study Designs

Case-series Studies Descriptive, not analytic –Not hypothesis driven Smaller sample size Specific population Tracks participants with known exposure, potentially based on similar treatment, and examines medical records for outcome. Follow-up

Case-Report Study A detailed report of the of an individual patient Symptoms Signs Diagnosis Treatment Follow-up Treatment Follow up Diagnosis Symptoms

Experimental Study Designs

Randomized Clinical Trial (RCT) Parallel, between-groups design –Can have more than two groups Investigator assigns treatment –Random assignment –Participants are blind to group assignment –Double-blind studies –Gold Standard

Quasi-experimental Design Same as RCT, with no random assignment –Treatment with or without control group –Effect of a specific intervention on a specific population –Groups may already be defined –Investigators may designate cutoffs for treatment vs. control –Pre-test Post-test design –Practice effects Target Population Selection Pre-test Intervention Post-test Pre-test Control Post-test

All Studies ExperimentalObservational Randomized Control Trial Non- randomized AnalyticDescriptive Case series Case reportsCohort Study Cross Sectional Case-Control Study Quasi- experimental

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Session Schedule All sessions held at the MVA from 12pm-1pm DateTopic June 19Literature Reviews & Grants 101 June 26Writing a Scientific Manuscript (Part 1) July 10Writing a Scientific Manuscript (Part 2) July 17Fundamentals of Study Design July 24Fundamentals of Biostatistics (Part 1) July 31Fundamentals of Biostatics (Part 2) To RSVP call (615) or