MedTrace Logo

Self-efficacy and Knowledge (SEEK) Trial to Improve Sexual Reproductive Health and Well-being for Syrian Refugee Women and Girls in Lebanon

NCT07008950 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 485

Last updated 2025-06-06

No results posted yet for this study

Summary

This community-based randomized controlled trial (RCT) aims to evaluate a low-resource/low-intensity integrated sexual reproductive health (SRH) and wellbeing intervention package. It will be delivered in Primary Healthcare Centres (PHCs) in a rural area in Lebanon to Syrian refugee women and girls aged 15-24.

Conditions

  • Mental Health Care
  • Sexual Health Quality of Life
  • Family Planning Services

Interventions

OTHER

The Self-Efficacy and Knowledge Trial

The intervention is composed on 8 sessions given over a period of 8 weeks covering topics of emotional regulation, communication, problem management, decision making, self-efficacy and others in relation to sexual reproductive health, family planning, and wellbeing. The intervention package will be delivered by trained non-specialists with at least 12 years of formal education. The package will be administered once a week for a duration of 90 minutes.

Sponsors & Collaborators

  • World Health Organization

    collaborator OTHER

  • Elrha

    collaborator OTHER

  • American University of Beirut Medical Center

    lead OTHER

Principal Investigators

  • Shadi Saleh, PhD · Global Health Institute American University of Beirut

  • Lale Say, MD · World Health Organization

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
15 Years
Max Age
15 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2025-05-01
Completion
2025-06-30

Countries

  • Lebanon

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07008950 on ClinicalTrials.gov