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People in detention in Geneva participating in research to improve their healthcare services

Not Applicable
Conditions
Healthcare services in detention
Not Applicable
Registration Number
ISRCTN45099461
Lead Sponsor
Division of Prison Health, Geneva University Hospitals and University of Geneva
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
100
Inclusion Criteria

People living in detention (PLD):
1. Adult (male, female, gender-fluid) without age restriction
2. Have demonstrated the ability to interact with one another in a respectful manner
3. Able to converse in French for the focus group discussion
4. Interested in the study and have given informed consent
5. Sufficient length of detention to match the sub-study period
6. For specific sub-studies: PLD with specific health conditions that are relevant to the topic of the sub-study

Key informants:
1. People who can provide specific insights into the health topic being researched (e.g. members of the detention authorities, social workers working in detention facilities, health professionals, among others)
2. Have given informed consent

Exclusion Criteria

1. Consent not given
2. In disciplinary confinement
3. Physical or mental conditions preventing taking part in participatory action research groups

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br> 1. Feasibility of participatory action research to improve the quality of care in detention settings<br> 2. Acceptability of participatory action research to improve the quality of care in detention settings<br><br>
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes will emerge from the participatory action research prioritization exercise. Each sub-study, in addition to contributing to understanding whether participatory action research is feasible and acceptable in improving quality of care in detention settings, will have their own secondary outcomes. These outcomes will be co-defined and the assessment tools co-designed in the PAR process of each sub-study.
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