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N/A N=161 Randomized Basic Science

Youth-friendly Sexual and Reproductive Healthcare Pilot in Mumbai, India

Reproductive Health

Enrolled (actual)
161
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: Change in Sexual and Reproductive Health and Rights Knowledge Survey Score — 0.45; 0.44; 0.47; 0.49 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Adolescent Health Club (Behavioral); Wait-list Control (Other)
Age
Pediatric, Adult · 15+ yrs
Sex
All
Sponsor
NYU Langone Health
Primary completion
Jul 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Sexual and Reproductive Health and Rights Knowledge Survey Score
0.45; 0.44; 0.47; 0.49
SECONDARY
Change in Clinic Service Uptake/Use: Change in Number of Requests for Contraception
-1; 0; -2; 1
SECONDARY
Change in Clinic Service Uptake/Use: Change in Number of Requests for Menstrual Health Materials/Support (MHM/S)
-1; 0; -4; -3
SECONDARY
Change in Clinic Service Uptake/Use: Change in Number of Requests for STI/HIV Tests
-2; 0; -4; 0
SECONDARY
Change in Personal and Community Safety
-0.14; -0.16; -0.43; -0.38
SECONDARY
Change in Gender Norms
0.16; 0.06; 0.07; 0.15
SECONDARY
Change in Perceived Self-efficacy and Agency
0.18; 0.51; 0.49; 0.46
SECONDARY
Change in Mental Health as Measured Using GAD-7
0.38; -1.55; -1.92; -1.76
SECONDARY
Change in Mental Health as Measured Using PHQ-8
0.30; -0.85; -1.23; -0.98
SECONDARY
Intervention Acceptability as Rated by AGYW
6.81; 6.64; 6.84; 6.89
SECONDARY
Satisfaction With Intervention/Services as Rated by AGYW
8.58; 8.63; 8.48; 8.39
SECONDARY
Intervention Feasibility as Rated by AGYW
5; 4.78; 5; 4.96

Summary

This study will systematically adapt, pilot test, and evaluate an integrated community/facility intervention to improve the uptake of adolescent-friendly services for married and unmarried adolescent girls and young women (AGYW; ages 15-25) in a low-income area with a population of approximately 700,000 in Mumbai, India

Eligibility Criteria

Inclusion Criteria

  • AGYW between the ages of 15-25 years old
  • Provide consent or assent,
  • Living in the study area for one year or more,
  • If unmarried and under the age of 18, have parental consent to participate. Married AGYW and/or those age 18 or over will be recruited if they meet inclusion criteria and provide informed consent.

Exclusion Criteria

  • AGYW who are unable to give consent due to psychological or mental limitations,
  • If unmarried and under the age of 18 do not have parental consent to participate.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04307849). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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