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One-time Informed Consent for Research in Prison

Not Applicable
Completed
Conditions
Informed Consent
Interventions
Behavioral: Audio-visual material
Registration Number
NCT05505058
Lead Sponsor
University Hospital, Geneva
Brief Summary

Ethical research on detained persons remains limited, including research on informed consent. This study aimed to fill in this research gap and compared audio-visual and paper-based materials for a one-time general informed consent for research in prison, using a randomized design. The primary outcome was whether participants sign the inform consent. Secondary outcomes included understanding, evaluation, and time to read/watch the informed consent.

Detailed Description

Detained persons constitute a very vulnerable and perhaps reluctant to share their medical data. In particular, it is crucial to ensure that these persons, deprived of their liberty, understand that their consent is voluntary and that a refusal will not have any consequence on their treatment or care. In other words, it is necessary to ensure that consent is informed. In a historical context of non-ethical research using detained persons, this is a crucial issue. However, while detained persons are now protected from various forms of abuse, this may have had the consequence of reducing research involving them, to the detriment of understanding their characteristics and vulnerabilities.

A general consent for research will encourage research on prison populations by facilitating access to their medical data in order to study and reduce health disparities, for this population with multiple somatic and psychiatric comorbidities.

Our main questions are:

Q1. What is the acceptability rate of general consent for research in detained persons? Q2. What are the characteristics (socio-demographic and medical) of detained person who refuse to give their consent? Q3. Which material (paper-based or video) is more effective?

To answer these research question, we will use an exploratory randomized cross-sectional trial, conducted in an adult pre-trial prison and a juvenile detention center. Participants will be randomly assigned to read or watch information about informed consent, stratified on the prison. In both prisons, the study will take place in the prison medical unit.

This project is aimed to improve general consent, which contributes to reducing inequalities in documentation on health status, and ultimately, health inequalities.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
290
Inclusion Criteria
  • to be18 years old or more in the adult prison and 14 years old or more in the juvenile detention center
  • to be able to communicate in one of the languages of the study material
  • to agree to participate in this study.
Exclusion Criteria
  • presence of an acute psychiatric problem preventing the person from participating in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Audio-visual materialAudio-visual materialThe video for informed consent was developed by a science filmmaker (https://www.lostlikebeesinrain.comhttps://betomation.space/) for the project's purposes.
Paper-based conventional materialAudio-visual materialThe written material for informed consent was developed by the Swiss Association of Research Ethic Committees and the booklet was designed by the Clinical Research Center of the Geneva University Hospitals.
Primary Outcome Measures
NameTimeMethod
Acceptance to sign the informed consentAssessed immediately after intervention

Binary outcome, legal Swiss document

Secondary Outcome Measures
NameTimeMethod
Time to read/watchAssessed immediately after intervention

Time in minutes for reading the booklet (the video has a unique duration of 4 min)

Evaluation of the informed consentAssessed immediately after intervention

Nine self-developed question assessed on a six-point Likert scale and averaged

Understanding of the informed consentAssessed immediately after intervention

Eight self-developed questions assessed as true/false and combined in a 0-8 points score

Trial Locations

Locations (1)

Division of prison health

🇨🇭

Geneva, Switzerland

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