ClinicalTrials.Veeva

Menu

Mitigating Adverse Sexual and Reproductive Health Outcomes Among Young Adolescents

M

Mbarara University of Science and Technology

Status

Unknown

Conditions

Relationship Problems Specific to Childhood and Adolescence

Treatments

Other: Lessons on comprehensive sexuality education

Study type

Interventional

Funder types

Other

Identifiers

NCT03669913
MUST 04/10-15

Details and patient eligibility

About

This study evaluates the effectiveness of comprehensive sexuality education (CSE) among young adolescents (10-14 years) in schools. A total of 33 schools will participate in the trial with 15 intervention arm that will receive CSE education and 18 in the control arm, Intervention will go on for one year

Full description

The International Technical Guidance on Sexuality Education (ITGSE) defines CSE as "an age-appropriate, culturally relevant approach to teaching about sexuality and relationships by providing scientifically accurate, realistic, non-judgmental information and CSE improves sexual and reproductive health outcomes of young people by delaying sexual debut, promoting condom use and increasing sexual health knowledge, however, most of these outcomes have been reported in older adolescents and there is limited evidence for effectiveness of CSE among young adolescents

The study aims at improving adolescent sexual and reproductive health of young adolescents through CSE that is led by interdisciplinary university students' team in an environment where no consistent or regulated sexual and reproductive health education program currently exists

Enrollment

1,100 estimated patients

Sex

All

Ages

10 to 14 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • adolescent 10-14 years in primary school
  • Adolescent in primary 5 or 6 of education in Uganda
  • Written consent/assent to participate

Exclusion criteria

  • Below 10 years or above 14 years at baseline
  • No consent obtained

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,100 participants in 2 patient groups

Intervention
Experimental group
Description:
Intervention arm will receive a pre evaluation survey, 11 lessons on CSE sequentially in a period of one year and a post evaluation survey
Treatment:
Other: Lessons on comprehensive sexuality education
Control arm
No Intervention group
Description:
This is a control arm that receives no intervention but will have and pre and post evaluation in one year

Trial documents
1

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems