Reducing HIV in Adolescents (RHIVA)
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The purpose of this study is to assess the impact of a cash-incentivised prevention intervention on reducing HIV incidence rates in high-school learners in rural KwaZulu-Natal.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Behavioral: Cash incentives Behavioral: Life skills curriculum |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | A Proof of Concept Cluster Randomised Controlled Trial to Evaluate the Impact of a Cash Incentivised Prevention Intervention to Reduce HIV Infection in High School Learners in Rural KwaZulu-Natal, South Africa |
- HIV-incidence rates [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]To evaluate the efficacy of a cash-incentivised prevention intervention in reducing HIV-incidence rates in high-school learners
- Academic performance measured as an overall passing grade (50%) [ Time Frame: 6 monthly ] [ Designated as safety issue: No ]To support learners improving academic performance, attend school, complete schooling and improve their self-esteem, learners will be incentivised to pass their June and November examinations, with a minimum of a 50% average. Educators from the selected schools will design, administer and mark the June and November examination papers.
- voluntary uptake of HIV testing [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]Learners must provide the receipt from the clinic that specifies that the learner was tested for HIV.
- Substance use patterns [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]Urine specimens will be utilised for testing for the presence of recreational drugs.
- Pregnancy rates in female learners [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]A dipstick pregnancy test will be performed on the urine sample of all female learners at baseline and at the two annual follow-up visits.
- Contraceptive use patterns in female learners [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]Annual behavioural questionnaires will monitor self-reported contraceptive use.
- Participation in extra-curricular activities [ Time Frame: annually, after every 12 months of follow up ] [ Designated as safety issue: No ]Attendance and participation in a life skills/sustainable livelihoods programme will be assessed. Self-reported participation in extra-curricular activities will be assessed in annual behavioural questionnaires.
- HIV risk reduction behaviour [ Time Frame: Annually, after every 12 months of follow up ] [ Designated as safety issue: No ]
The following will be assessed through a self-reported questionnaire:
condom use; primary and/or secondary sexual abstinence rates; sexually transmitted disease rates intergenerational sexual coupling (age of sexual partner(s)) age of sexual debut; frequency of HIV testing; number of concurrent sex partners; frequency of partner change; medical male circumcision rates; anal sex rates
| Estimated Enrollment: | 4000 |
| Study Start Date: | September 2010 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Control
All eligibly enrolled learners in the intervention schools will receive a prevention program delivered by MIET Africa and the KwaZulu-Natal Department of Education. No cash incentives will be paid for meeting milestones
|
Behavioral: Life skills curriculum
Standard department of education lifeskills curriculum
|
|
Experimental: Cash incentive
All eligibly enrolled learners in the intervention schools will receive a cash incentivised prevention program delivered by MIET Africa and the KwaZulu-Natal Department of Education
|
Behavioral: Cash incentives
Cash incentives paid to learners for reaching pre-determined milestones
|
Detailed Description:
The impact of the cash incentivised intervention will be assessed using a matched pair, cluster randomised controlled trial design. The 14 selected high schools in the Vulindlela School Circuit will be matched in pairs. The matched pairs of schools will be the unit of randomisation. Baseline measurements, using a standardised tool (structured questionnaire and biological specimens) will be undertaken simultaneously in each matched pair and will include all eligibly enrolled and consenting learners in the respective schools. On completion of baseline measurements in each matched pair of schools, the randomisation code for the pair will be revealed and the intervention will be implemented in the intervention school. All schools will receive the same prevention intervention but only the intervention school will receive the cash incentives. Follow-up measurements will be undertaken approximately 12 and 24 months after implementation of the intervention using a similar standardised assessment tool to that used at baseline. At baseline and during follow-up assessments in intervention and control schools, linked HIV and substance use testing will be undertaken in all learners and pregnancy testing in female learners. Other secondary endpoints will be assessed using a structured questionnaire.
Eligibility| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Learners must meet all of the following criteria at enrolment in order to be eligible for inclusion in the study:
- Male or female learner in Grade 9 or 10 in one of the 14 selected schools
- Willing and able to provide informed consent and/or assent to participate in the study
- Willing to provide locator data for home visits if necessary
- Not planning to move to another school or relocate in the next 36 months
- Willing to be finger-printed to verify identity for study procedure purposes
- Willing to participate in this study
- Willing to complete all study procedures
Exclusion Criteria:
- Refusal by the learner and/or parent or legal guardian to participate in the study.
- Unable to provide necessary informed consents
- Cognitively challenged learners
Contacts and Locations| South Africa | |
| Vulindlela Clinical Research Site | |
| Durban, KwaZulu-Natal, South Africa | |
| Principal Investigator: | Quarraisha Abdool Karim, PhD | Associate Scientific Director |
More Information
Additional Information:
Publications:
| Responsible Party: | Dr Quarraisha Abdool Karim, Principal Investigator and Protocol Chair, Centre for the AIDS Programme of Research in South Africa |
| ClinicalTrials.gov Identifier: | NCT01187979 History of Changes |
| Other Study ID Numbers: | CAPRISA 007 |
| Study First Received: | August 12, 2010 |
| Last Updated: | February 23, 2012 |
| Health Authority: | South Africa: National Health Research Ethics Council |
Keywords provided by Centre for the AIDS Programme of Research in South Africa:
|
Cash incentive HIV prevention Adolescents South Africa HIV |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on May 19, 2013