Eurosupport 6: Testing the effectiveness of a computer-assisted counselling intervention on safer sex (CISS) for people living with HIV (PLHIV)
Completed
- Conditions
- human immuno-deficiency virus infectionHIV10047438
- Registration Number
- NL-OMON34668
- Lead Sponsor
- Institute of Tropical Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
-Being over 18 years of age;
-Having received their HIV-diagnosis a minimum of 6 months ago;
-Migrant status (man or woman) or man who has sex with other men (MSM)
-Understand the study goal, purpose and procedures involved;
-Having given their informed consent.
Exclusion Criteria
-Being under 18 years of age;
-Having received their HIV diagnosis less than 6 months ago;
-No migrantstatus or MSM
-A language barrier prevents counselling possibility;
-Not understanding the study*s purpose and procedures and therefore unable to give informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Over the whole study period, data are collected on the primary and secondary<br /><br>outcomes. Data are collected using a computerised system, i.e. study<br /><br>participants fill out the questionnaire on a PC provided at the clinic, using<br /><br>Snap®-software.<br /><br>Data assessments occur at 5 points in time: screening, baseline assessment,<br /><br>post-intervention assessment, and at 3- and 9-months after completion of the<br /><br>intervention.<br /><br>Note that not all study variables are assessed at each assessment: overview of<br /><br>study variables and the moments of assessment are given in annex 5.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Seen Annex 5 of the study protocol</p><br>