Back to search

Article

Sociodemographic Predictors of Consent: A Protocol and Statistical Analysis Plan for a Nested Observational Study of Canadian Sites in the REVISE Trial

2026-07-09

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Background</h4> In Canada, there is a lack of data relating sociodemographic characteristics to the likelihood of consent and clinical trial participation. <h4>Objective</h4> The overall objective of this study is to examine the association of hospital-level sociodemographic variables with a priori informed consent rates for participation in the REVISE trial. <h4>Design</h4> This study...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
a11864ec-3ac3-5e92-b9fb-0245bc33745b
DOI
10.64898/2026.07.06.26357216
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Sociodemographic Predictors of Consent: A Protocol and Statistical Analysis Plan for a Nested Observational Study of Canadian Sites in the REVISE TrialDOI 10.64898/2026.07.06.26357216
Sociodemographic Bias in Large Language Model Clinical Trial ScreeningSemantic proximity
Developing and validating a clinical prediction model to predict epilepsy-related hospital admission or death within the next year using administrative healthcare data: a population-based cohort study protocolSemantic proximity
Demographic Representation of a Decentralized Long COVID Trial: A Comparison with the 2023 National Health Interview SurveySemantic proximity
Inclusion in clinical research: cross-sectional study assessing potential barriers to informed consent in randomized controlled trials published in top general and internal medical journalsSemantic proximity
Consent to Recontact for Future Research Using Linked Primary Healthcare Data: Outcomes and General Practice Perceptions from the ATHENA COVID-19 StudySemantic proximity
Reporting of socio-demographic characteristics of trial participants in infectious diseases clinical trials – a systematic reviewSemantic proximity
A Framework for Inclusive and Accessible Clinical Research in Rare DiseasesSemantic proximity
Perception of Informed Consent and Its Associated Factors among Surgical Patients Attending Public Hospitals in North Shoa Zone, Oromia, Ethiopia, 2024: A Mixed Method StudySemantic proximity
Community and academic hospitals participating in a randomized trial: Patient characteristics, research capacity and trial metricsSemantic proximity
The First General Consent Implementation in Swiss Traditional Chinese Medicine Practices. A Prospective One-Year StudySemantic proximity
Assessment of the Appropriateness of the i-CONSENT Guideline Recommendations for Improving Understanding of the Informed Consent Process in Clinical StudiesSemantic proximity
Current State and Demographic Trends of Medically Underserved Populations in Rare Disease Research in the United StatesSemantic proximity
Select a neighboring publication to make it the new centre.