Self-efficacy and Knowledge (SEEK) Trial to Improve Sexual Reproductive Health and Well-being for Syrian Refugee Women and Girls in Lebanon
American University of Beirut Medical Center
485 participants
Jan 1, 2024
INTERVENTIONAL
Conditions
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.
Eligibility
Inclusion Criteria4
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- are currently married and between the ages of 15 - 24 years,
- completed an average stay in Lebanon for a minimum of 6 months,
- are willing to take part in the study as indicated by them signing an informed consent (for young women 18 years of age or older) or through a legal guardian consent form and written assent for adolescents' girls between 15 and 17,
Exclusion Criteria5
- Participants will be excluded from the study if they meet any of the following criteria:
- are currently pregnant and/or lactating,
- have reported chronic health problems interfering with the ability to follow the intervention protocol,
- have high levels of anxiety and/or depression as well as suicidal ideations and/or attempts upon screening and/or a current diagnosis of a severe mental illness, or undergoing mental health treatment.
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Interventions
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.
Locations(1)
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NCT07008950