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This document outlines the essential features of systematic reviews with a focus on coding protocols, eligibility criteria, and screening forms, adapted from the methodologies of David B. Wilson and Mark W. Lipsey. It aims to provide a transparent and replicable framework for study descriptions, findings extraction, and coding reliability assessment. The guide covers common mistakes in study eligibility, coding practice exercises, and development of coding protocols, ensuring effectiveness in reviewing data accuracy and quality.
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C2 Training: May 9 – 10, 2011 Data Evaluation: Initial screening and Coding Adapted from David B. Wilson and Mark W. Lipsey
Overview • Coding protocol: essential feature of systematic review • Goal: transparent and replicable • description of studies • extraction of findings • Forms should be part of C2 protocol
Topics • Eligibility criteria and screening form • Development of coding protocol • Assessing reliability of coding • Common mistakes
Study Eligibility Criteria • Flow from research question • Identify specifics of: • Defining features of the program/policy/intervention • Eligible designs; required methods • Key sample features • Required outcomes • Required statistical data • Geographical/linguistic restrictions, if any • Time frame, if any • Also explicitly states what is excluded
Study Eligibility Screening Form • Develop a screening form with criteria • Complete form for all studies retrieved as potentially eligible • Modify criteria after examining sample of studies (controversial) • Double-code eligibility • Maintain database on results for each study screened • Example from MST review in handouts
Screening Form Effects of Multisystemic Therapy (MST) Initial Screening Form 1.0
Effects of Multisystemic Therapy (MST): Eligibility Screening Form 1.2
Screening Coding Guide for “Internet-based Interventions for English Language Learners”
Coding practice exercise 1 • For the articles provided, code Levels 1 and 2 from the MST coding sheet • Use Brunk and either Bourduin or Henggler & Melton
Development of Coding Protocol • Goal of protocol • Describe studies • Differentiate studies • Extract findings (effect sizes if possible) • Coding forms and manual • Both important • Sample coding item from form • Sample manual instructions for item
Development of Coding Protocol • Types of Information to Code • Setting, study context, authors, publication date and type, etc. • Methods and method quality • Program/intervention • Participants/clients/sample • Outcomes • Findings, effect sizes
Types of Information to Code • Setting, study context, authors, publications date and type, etc. • Multiple publications; “study” vs “report” • Geographical/national setting; language • Publication type and publication bias issue • Publication date vs study date • Research, demonstration, practice studies • Example from MST review in handouts
Types of Information to Code • Methods: Basic research design • Nature of assignment to conditions • Attrition, crossovers, dropouts, other changes to assignment • Nature of control condition • Multiple intervention and/or control groups • Design quality dimensions • Initial and final comparability of groups • Treatment-control contrast • treatment contamination • blinding
Types of Information to Code • Methods: Other aspects • Issues depend on specific research area • Procedural, e.g., • monitoring of implementation, fidelity • credentials, training of data collectors • Statistical, e.g., • statistical controls for group differences • handling of missing data
Types of Information to Code • Method quality ratings (or not) • More than 200 scales and checklists available, few if any appropriate for systematic reviews (Deeks et al., 2003) • Overall study quality scores have questionable reliability/validity (Jüni et al., 2001) • Conflate different methodological issues and study design/implementation features, which may have different impacts on reliability/validity • Preferable to examine potential influence of key components of methodological quality individually • Weighting results by study quality scores is not advised!
Cochrane risk of bias framework • Focus on identifying potential sources of bias in studies: • Selection bias - Systematic differences between groups at baseline • Performance bias - Something other than the intervention affects groups differently • Attrition bias - Participant loss affects initial group comparability • Detection bias - Method of outcome assessment affects group comparisons • Reporting bias - Selective reporting of outcomes
GRADE system for method quality • Quality of evidence across trials • Outcome-specific • Considers: sparse data, consistency/inconsistency of results across trials, study designs, reporting bias, possible influence of confounding variables • Software available at: www.ims.cochrane.org/revman/gradepro • Also see: www.gradeworkinggroup.org
Types of Information to Code • Program/Intervention • General program type (mutually exclusive or overlapping?) • Specific program elements (present/absent) • Any treatment received by the comparison group • Treatment implementation issues • integrity • amount, “dose” • Goal is to differentiate across studies • Examples
Types of Information to Code • Participants/clients/sample • Data is at aggregate level • Mean age, age range • Gender mix • Racial/ethnic mix • Risk, severity • Restrictiveness; special groups (e.g., clinical) • Examples
Types of Information to Code • Outcome measures • Construct measured • Measure or operationalization used • Source of information • Composite or single indicator (item) • Scale: dichotomous, count, discrete ordinal, continuous • Reliability and validity • Time of measurement (e.g., relative to treatment) • Examples
Types of Information to Code • Findings • Compute effect sizes when possible • May need to aggregate data or reconfigure findings • Add back the “dropouts” • Compute weighted means of subgroups (e.g., boys and girls) • Code data on which computations based (common situations) • We will look at this part of the coding in the next section
Development of Coding Protocol • Iterative nature of development • Structuring data • Data hierarchical (findings within studies) • Coding protocol needs to allow for this complexity • Analysis of effect sizes needs to respect this structure • Flat-file (example) • Relational hierarchical file (example)
Data extraction Double data extraction • Cohen’s kappa • Agreement on key decisions • Study inclusion/exclusion, key characteristics, risk of bias, coding of results • Pilot-test and refine codes!
Example of a Flat File Multiple ESs handled by having multiple variables, one for each potential ES. Note that there is only one record (row) per study
Example of a Hierarchical Structure Study Level Data File Effect Size Level Data File Note that a single record in the file above is “related” to five records in the file to the right
Coding exercise 2 • For either Borduin or Henggler & Melton, please code the Level 3 items (do not do the outcomes and effect sizes) • Report back: what was easy/difficult?