Assessing smoking status in disadvantaged populations: is computer administered self report an accurate and acceptable measure?
Reaching the hard-to-reach: a systematic review of strategies for improving health and medical research with socially disadvantaged groups
Recruitment of representative samples for low incidence cancer populations: do registries deliver?
Moderate agreement between self-reported stroke and hospital-recorded stroke in two cohorts of Australian women: a validation study
Agreement between self-reported and measured weight and height collected in general practice patients: a prospective study
Consent to data linkage in a large online epidemiological survey of 18–23 year old Australian women in 2012–13
The quality of the evidence base for clinical pathway effectiveness: room for improvement in the design of evaluation trials
A randomized controlled trial of the effectiveness of a pre-recruitment primer letter to increase participation in a study of colorectal screening and surveillance.
A consumer register: an acceptable and cost-effective alternative for accessing patient populations
Factors associated with retention in a smoking cessation trial for persons with a mental illness: a descriptive study
Integrating and extending cohort studies: lessons from the eXtending Treatments, Education and Networks in Depression (xTEND) study
Can obtaining informed consent alter self-reported drinking behaviour? A methodological experiment
Exploratory randomized controlled trial evaluating the impact of a waiting list control design
A self-controlled case series to assess the effectiveness of beta blockers for heart failure in reducing hospitalisations in the elderly
Stepped wedge cluster randomised trials: a review of the statistical methodology used and available
The reliability of a quality appraisal tool for studies of diagnostic reliability (QAREL)
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