Mental and Reproductive Health Integration and Access

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15-49
SponsorEastern Mediterranean Public Health Network

About this trial

The goal of this clinical trial is to learn whether an integrated package of mental health screening, brief psychosocial support, and family planning counseling delivered within routine postnatal care can improve reproductive and mental health outcomes in postpartum migrant, refugee, and underserved Jordanian women aged 15-49 attending primary health centers in Mafraq Governorate and the Al-Ghour region of Jordan. The main questions it aims to answer are:

1. Does the MARIA intervention increase the use of modern contraceptive methods among postnatal women compared to standard care? 2. Does the MARIA intervention reduce the prevalence and severity of postpartum depression symptoms compared to standard care?

Researchers will compare women attending health centers that deliver the full MARIA package (integrated mental health screening, brief psychosocial support, and family planning counseling) to women attending health centers that provide standard care (routine immunization and child health services without the MARIA components) to see if the intervention improves contraceptive use and reduces postpartum depression.

Participants will:

* Complete a 10-question mental health screening tool (Edinburgh Postnatal Depression Scale) at their routine immunization visit * Receive a brief educational session, psychosocial support, or a referral to specialist mental health services - depending on their screening result * Receive family planning counseling and information about contraceptive options during the same visit * Be followed up by a community health worker, as needed * Participate in three interviews - one in person at enrollment and two by telephone at 4 and 7 months after joining

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Postpartum women aged 15-49 years

Attending selected primary healthcare centers for infant immunization or healthy child visits

Unmet family planning need: interested in using contraception but currently not doing so

Living in study villages (Mafraq or Al-Ghour)

Disqualifiers

Currently using a modern contraceptive method

Unmarried women

Unable to provide informed consent

Planning to leave the study area within 7 months

Trial design

Design model

Parallel

Treatments tested in this trial

  • MARIA Integrated Maternal Mental Health and Family Planning Package

    Behavioral

    A multi-component integrated package delivered within routine postnatal and immunization visits at primary healthcare centers. Has 7 components 1. Integrated service delivery: All eligible postnatal women are screened for postpartum depression using Edinburgh Postnatal Depression Scale. Based on score, primary healthcare providers deliver stepped-care psychosocial support. Family planning counseling is integrated into the same visit for all women. 2. Community health workers community outreach 3. Provider training 4. Supportive Supervision 5. Communication/educational material (brochures, pamphlets, videos in waiting area) 6. A project website and automated electronic Edinburgh Postnatal Depression Scale tool accessible via QR code for use by providers, community health workers, and women 7. online learning courses on implementation research and leadership and management

Treatment groups

920 Participants
are divided into 2 treatment groups
Group A: MARIA Integrated Family Planning and Mental Health InterventionExperimental treatment 1 intervention
Group B: Standard Care (Control)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Number of Participants adopting any modern contraceptive method since baseline

Time frame
from baseline until 7 months

Secondary outcomes

1

number of women with postpartum depression

Edinburgh Postnatal Depression Scale

Time frame
from baseline until 7 months
2

number of women who continue the modern contraception

Time frame
at the end of the 7 months follow up
3

change in baseline in the number of women who feel empowered

Oxfam Women's Empowerment Measurement Tool

Time frame
at 7 months
4

change in baseline in the number of women with positive attitude towards pregnancy

Attitude Toward Potential Pregnancy Scale (APPS)

Time frame
at 7 months

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: