Actively Recruiting

Phase Not Applicable
Age: 15Years - 15Years
FEMALE
Healthy Volunteers
NCT07008950

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

Led by American University of Beirut Medical Center · Updated on 2025-06-06

485

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

Sponsors

A

American University of Beirut Medical Center

Lead Sponsor

W

World Health Organization

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 15Years - 15Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female Syrian adolescent girls and young women aged 15 to 24 years
  • Currently married
  • Residing in Beqaa governorate, Lebanon
  • Have lived in Lebanon for at least 6 months
  • Provide signed informed consent (or guardian consent and assent for ages 15-17)
Not Eligible

You will not qualify if you...

  • Currently pregnant or breastfeeding
  • Having chronic health problems that interfere with following the study protocol
  • Experiencing high levels of anxiety, depression, suicidal thoughts or attempts
  • Diagnosed with severe mental illness or undergoing mental health treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

American University of Beirut

Beirut, Lebanon, 00000

Actively Recruiting

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Research Team

S

Shadi Saleh, PhD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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