Integrated digital e-clinic for mental health and reproductive health for women and adolescent girls in Jordan

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This implementation study evaluates an integrated digital e-clinic that delivers mental health and psychosocial support alongside reproductive health information for women and adolescent girls in Jordan. It uses a single-group pre-post design to measure changes in mental health and well-being, digital health literacy, reproductive health knowledge, and service use over about three months. Participants access individualized support, educational resources, and referral pathways remotely, with safety and urgent care procedures in place when needed. Outcomes include depressive, anxiety, and PTSD symptoms, psychological well-being, health literacy, attitudes toward reproductive health, and user satisfaction and engagement with the platform. Process indicators track sessions, resource use, referrals, and platform engagement.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Female participants aged 14 to 65 years.
* Jordanian women and adolescent girls and Syrian refugee women and adolescent girls residing in Jordan.
* Eligible to receive psychosocial, mental-health and/or reproductive-health support through the e-clinic.
* Able to access the e-clinic using an internet-connected device or another approved method of access.
* Willing to participate in the e-clinic intervention and study assessments. Able to provide informed consent.
* For participants below the age at which independent consent is permitted under the approved protocol, parental/legal guardian consent and adolescent assent will be obtained.

Exclusion Criteria:

* Acute psychiatric or psychological condition requiring immediate specialist or emergency intervention beyond the scope of the e-clinic.
* Imminent risk of suicide or serious self-harm requiring emergency assessment or intervention.
* Acute medical or reproductive-health emergency requiring urgent face-to-face care.
* Inability to provide informed consent/assent or participate meaningfully in the intervention and assessments.
* Circumstances in which remote participation cannot be conducted safely according to the study safety protocol.

Where it's running

• Jordan University of Science and Technology
  Irbid, Jordan Recruiting

Study contacts

• Principal investigator: Mohammad S Alyahya — Jordan University of Science and Technology
• Study coordinator: Mohammad Sharif Alyahya, PhD
• Email: msalyahya@just.edu.jo
• Phone: +962 775582824

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.