Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Contraception
  • Pregnancy Related
  • Reproductive Behavior
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This is an individually randomized parallel group study design.Masking: Triple (Participant, Investigator, Outcomes Assessor)Masking Description: Participants are blinded through the study arm and the outcomes assessor and investigator are blinded to participant group assignment for the intervention.Primary Purpose: Health Services Research

Participation Requirements

Age
Between 15 years and 19 years
Gender
Only males

Description

The PREVENT study seeks to impact knowledge, perceptions, and behavioural changes regarding SRH among adolescent girls. As a result, the data collected in the PREVENT study will be grouped into two main themes: SRH knowledge and attitudes, as well as family planning (pregnancy avoidance) and contrac...

The PREVENT study seeks to impact knowledge, perceptions, and behavioural changes regarding SRH among adolescent girls. As a result, the data collected in the PREVENT study will be grouped into two main themes: SRH knowledge and attitudes, as well as family planning (pregnancy avoidance) and contraceptive services uptake and outcomes. All data collected during the study will be directly entered and stored into the secure PREVENT mobile platform and related secure storage functions within the platform.

Tracking Information

NCT #
NCT03995043
Collaborators
Not Provided
Investigators
Not Provided