Testing a New Method to Improve Informed Consent in Prison Research
Recruiting · NCT06378281 · Interventional (participants receive a specific treatment) · Lead sponsor: Stéphanie Baggio
View the official record on ClinicalTrials.gov →Interventions studied
Modified teach-to-goal informed consent
What this trial is about
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.
Who can take part
Age range
18 Years to 65 Years
Sex
Male
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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.
Where it is running
2 locations listed.
- Geneva University Hospitals - Geneva, Canton of Geneva, Switzerland
- Geneva University Hospitals - Geneva, Canton of Geneva, Switzerland