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Reducing HIV in Adolescents (RHIVA)

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 2
Locations
South Africa
Study Type
Interventional
Intervention
Cash incentives
Life skills curriculum
Sponsored by
Centre for the AIDS Programme of Research in South Africa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Cash incentive, HIV prevention, Adolescents, South Africa, HIV

Eligibility Criteria

13 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Vulindlela Clinical Research Site

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control

Cash incentive

Arm Description

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

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

Outcomes

Primary Outcome Measures

HIV-incidence rates
To evaluate the efficacy of a cash-incentivised prevention intervention in reducing HIV-incidence rates in high-school learners

Secondary Outcome Measures

Academic performance measured as an overall passing grade (50%)
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
Learners must provide the receipt from the clinic that specifies that the learner was tested for HIV.
Substance use patterns
Urine specimens will be utilised for testing for the presence of recreational drugs.
Pregnancy rates in female learners
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
Annual behavioural questionnaires will monitor self-reported contraceptive use.
Participation in extra-curricular activities
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
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

Full Information

First Posted
August 12, 2010
Last Updated
January 18, 2017
Sponsor
Centre for the AIDS Programme of Research in South Africa
Collaborators
MIET Africa, KwaZulu-Natal Department of Education, Embassy of the Kingdom of the Netherlands (EKN)
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1. Study Identification

Unique Protocol Identification Number
NCT01187979
Brief Title
Reducing HIV in Adolescents
Acronym
RHIVA
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
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
September 2010 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre for the AIDS Programme of Research in South Africa
Collaborators
MIET Africa, KwaZulu-Natal Department of Education, Embassy of the Kingdom of the Netherlands (EKN)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Cash incentive, HIV prevention, Adolescents, South Africa, HIV

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3217 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
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
Arm Title
Cash incentive
Arm Type
Experimental
Arm Description
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
Intervention Type
Behavioral
Intervention Name(s)
Cash incentives
Intervention Description
Cash incentives paid to learners for reaching pre-determined milestones
Intervention Type
Behavioral
Intervention Name(s)
Life skills curriculum
Intervention Description
Standard department of education lifeskills curriculum
Primary Outcome Measure Information:
Title
HIV-incidence rates
Description
To evaluate the efficacy of a cash-incentivised prevention intervention in reducing HIV-incidence rates in high-school learners
Time Frame
annually, after every 12 months of follow up
Secondary Outcome Measure Information:
Title
Academic performance measured as an overall passing grade (50%)
Description
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.
Time Frame
6 monthly
Title
voluntary uptake of HIV testing
Description
Learners must provide the receipt from the clinic that specifies that the learner was tested for HIV.
Time Frame
annually, after every 12 months of follow up
Title
Substance use patterns
Description
Urine specimens will be utilised for testing for the presence of recreational drugs.
Time Frame
annually, after every 12 months of follow up
Title
Pregnancy rates in female learners
Description
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.
Time Frame
annually, after every 12 months of follow up
Title
Contraceptive use patterns in female learners
Description
Annual behavioural questionnaires will monitor self-reported contraceptive use.
Time Frame
annually, after every 12 months of follow up
Title
Participation in extra-curricular activities
Description
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.
Time Frame
annually, after every 12 months of follow up
Title
HIV risk reduction behaviour
Description
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
Time Frame
Annually, after every 12 months of follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Quarraisha Abdool Karim, PhD
Organizational Affiliation
Associate Scientific Director
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vulindlela Clinical Research Site
City
Durban
State/Province
KwaZulu-Natal
Country
South Africa

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
16135907
Citation
Pettifor AE, Rees HV, Kleinschmidt I, Steffenson AE, MacPhail C, Hlongwa-Madikizela L, Vermaak K, Padian NS. Young people's sexual health in South Africa: HIV prevalence and sexual behaviors from a nationally representative household survey. AIDS. 2005 Sep 23;19(14):1525-34. doi: 10.1097/01.aids.0000183129.16830.06.
Results Reference
background
PubMed Identifier
18558031
Citation
Fernald LC, Hou X, Gertler PJ. Oportunidades program participation and body mass index, blood pressure, and self-reported health in Mexican adults. Prev Chronic Dis. 2008 Jul;5(3):A81. Epub 2008 Jun 15.
Results Reference
background
PubMed Identifier
12031070
Citation
Hargreaves JR, Glynn JR. Educational attainment and HIV-1 infection in developing countries: a systematic review. Trop Med Int Health. 2002 Jun;7(6):489-98. doi: 10.1046/j.1365-3156.2002.00889.x.
Results Reference
background
PubMed Identifier
32747693
Citation
Ayton SG, Pavlicova M, Abdool Karim Q. Identification of adolescent girls and young women for targeted HIV prevention: a new risk scoring tool in KwaZulu Natal, South Africa. Sci Rep. 2020 Aug 3;10(1):13017. doi: 10.1038/s41598-020-69842-x.
Results Reference
derived
Links:
URL
http://www.caprisa.org/
Description
CAPRISA website

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Reducing HIV in Adolescents

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