'HI-4-TU' Study: Health Improvement for Teen Ugandans Study
- Conditions
- Human Immunodeficiency VirusSexually Transmitted DiseasesPregnancy
- Interventions
- Behavioral: enhanced group supportBehavioral: enhanced individual support
- Registration Number
- NCT02845284
- Lead Sponsor
- Johns Hopkins University
- Brief Summary
This randomized clinical trial is an adolescent focused implementation science study directed at improved social support and prevention of both HIV/STI's and subsequent unplanned pregnancies. The study population is pregnant adolescents who are attending antenatal care in Kampala, Uganda The acceptability and effectiveness of two enhanced peer lead, reproductive health promotion interventions compared to routine health care will be studied. The study participants will be individually randomized to one of three arms.
- Detailed Description
The overall goal of this research to test the acceptability and effectiveness of two enhanced adolescent friendly reproductive health prevention interventions versus current routine care. In each intervention group, 152 adolescent mothers will be randomized to either the enhanced group peer support education and counseling intervention or to the enhanced one-to-one (individual) peer support education and counseling group with a young, model, peer educator trained to deliver Reproductive Health Education and counseling messages, beginning during pregnancy (≥ 28 weeks) and followed up to 9 months postpartum or study end at or after 6 months (whichever comes first). The control group will consist of 215 adolescent mothers randomized to routine care as provided at Mulago hospital (or the designated health facility) where midwives deliver group sessions during antenatal and postpartum care visits as well as standard PMTCT services including routine opt-out HIV C\&T and availability of partner C\&T. Syphilis testing should also be routinely provided and treatment provided for infected pregnant mothers and their partners as per local standard of care.
The 3 groups will be enrolled with study visits at 3, 6 and 9 months post partum however the intervention groups (Arms 2 and 3) will have additional visits at 36 weeks Antepartum, delivery, 6 and 10 weeks postpartum, Quantitative baseline data will be collected on routine demographic characteristics, reproductive history, pregnancy intentions and sexual risk/perceptions and HIV/Sexually Transmitted Infection status.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 486
- Pregnant at ≥28 weeks of gestation
- Agreeing to provide written informed consent to be screened for and take part in the study
- Agreeing to provide adequate locator information with residence within 30 km
- Agreeing to a home visit
- Agreeing to come for follow up visits and to receive study follow up phone calls
- Serious illness or social conditions that would prevent adherence to study requirements
- High risk pregnancy or fetal death in utero (with the exception of risk defined only by maternal age)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Routine Care plus group support enhanced group support Routine Care plus enhanced group support Routine Care plus individual support enhanced individual support Routine Care plus enhanced individual support
- Primary Outcome Measures
Name Time Method Composite measure of consistent condom-use and use of an effective family planning method method A comparison of this binary outcome will be conducted at one year. A log-binomial regression model will be used to obtain the prevalence rate ratios.
Incidence of any Sexually Transmitted Infection at one year Kaplan-Meier survival analysis will be conducted to determine differences in the probability of sexually transmitted infection between study arms.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
MUJHU CARE Ltd
🇺🇬Kampala, Wakiso DIstrict, Uganda