Testing a New Method to Improve Informed Consent in Prison Research

Recruiting N/A Interventional Study
ADHD
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 65
Sex
Male
Study type
Interventional
Purpose
Basic Science
Participants needed
100 (estimated)
Sponsor
Stéphanie Baggio · Other
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About This Trial

Understanding of informed consent is often limited in prison, due to unique challenges faced by detained people. This study will test a modified "teach-to-goal" informed consent process compared to standard procedures. Conducted within a larger study on psychiatric outcomes, it aims to enhance ethical practices for vulnerable populations.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * inclusion in the parent-RCT * age ≥ 18 years * good command of French * absence of acute psychiatric disorder * providing written informed consent for study participation in the parent-RCT Exclusion Criteria: \- none.
Contacts

Stéphanie Baggio, Prof.

+41216923238

stephanie.baggio@unil.ch

CONTACT