Intervention for (Those) Recently Informed of Seropositive Status (IRISS)
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Details and patient eligibility
About
An intervention designed to increase positive affect in a population newly diagnosed with HIV will be effective at improving affect and HIV-related outcomes such as mental and physical health, coping and coping resources.
Full description
The study is a randomized controlled trial of a 5-session positive affect skills intervention compared to an attention-matched control condition. Participants will be 200 men and women who have tested positive for HIV within the past 12 weeks. Both intervention and control sessions will be approximately one hour long and will be administered one-on-one by trained facilitators. Both groups will have daily home practice over the 5 weeks of the intervention. At the end of the assessment period, participants in the control condition will have the opportunity to attend a ½ day group session that provides a condensed version of the positive affect skills taught in the intervention condition. Participants will complete assessments at four points and CD4 and viral load assays will be run at 3 time points.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- have been informed they were HIV positive within the past 12 weeks
- speak English or Spanish
- be 18 years or older
- have the ability to provide informed consent to be a research participant.
Exclusion criteria
- inability to provide informed consent, as evidenced by cognitive impairment as assessed by trained interviewers and confirmed by a licensed clinical psychologist
- active psychosis as assessed by trained interviewers and confirmed by clinical psychologist
Trial design
Primary purpose
Allocation
Interventional model
Masking
160 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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