Front page
Handbook information
Part 1: Cochrane reviews
Part 2: General methods for Cochrane reviews
    5 Defining the review question and developing criteria for including studies
    6 Searching for studies
    7 Selecting studies and collecting data
    8 Assessing risk of bias in included studies
       8.1 Introduction
       8.2 What is bias?
       8.3 Tools for assessing quality and risk of bias
       8.4 Introduction to sources of bias in clinical trials
       Table 8.4.a: A common classification scheme for bias
       8.5 The Cochrane Collaboration's tool for assessing risk of bias
       8.6 Presentation of assessments of risk of bias
       Figure 8.6.a: Example of a 'Risk of bias' table
       Figure 8.6.b: Example of a 'Risk of bias graph' Figure
       Figure 8.6.c: Example of a 'Risk of bias summary' Figure
       8.7 Summary assessments of risk of bias
       Table 8.7.a: Possible approach for summary assessments
       8.8 Incorporating assessments into analyses
       8.9 Sequence generation
       8.10 Allocation sequence concealment
       8.11 Blinding of participants and personnel
       8.12 Blinding of outcome assessment
       8.13 Incomplete outcome data
       8.14 Selective outcome reporting
       8.15 Other potential threats to validity
          8.15.1 Rationale for concern about bias
             Introductory text
    Design-specific risks of bias
    Baseline imbalance
    Blocked randomization in unblinded trials
    Differential diagnostic activity
    Further examples of potential biases
          8.15.2 Assessing risk of bias from other sources
       8.16 Chapter information
       8.17 References
    9 Analysing data and undertaking meta-analyses
    10 Addressing reporting biases
    11 Presenting results and 'Summary of findings' tables
    12 Interpreting results and drawing conclusions
Part 3: Special topics
Additional material