Skip to content

The Effects of Empowerment with Husband's Engagement Program on Intention of Continuing Education and Self-Efficacy in Performing the Maternal Role of First-Time Pregnant Adolescents: A Randomized Controlled Trial

The Effects of Empowerment with Husband's Engagement Program on Intention of Continuing Education and Self-Efficacy in Performing the Maternal Role of First-Time Pregnant Adolescents: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251129007
Enrollment
108
Registered
2025-11-29
Start date
2025-11-24
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent Pregnancy Pregnancy in Adolescence Adolescent Pregnancy Teenage Pregnancy Primigravida Empowerment Husbands Spouses Engagement Participation Intention Continuing Education Self Efficacy Maternal Role Randomized Controlled Trial

Interventions

In the experimental group, participants will receive usual care at the antenatal clinic in the hospital. Also, they will receive the empowerment with the husband engagement program as scheduled. They
Experimental Other,No Intervention No treatment
Experimental group,Control group

Sponsors

Graduate School, Prince of Songkla University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
13 Years to 19 Years

Inclusion criteria

Inclusion criteria: 1. First-time pregnant 2. Age from 13 to 19 years old 3. Gestational age between 15-24 weeks 4. Living with husband 5. Able to understand, speak, and write Thai language

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1. Have a history of severe mental health conditions, such as depression or schizophrenia, who are currently undergoing treatment. 2. Have a history of substance use during pregnancy. 3. Husbands of pregnant adolescents do not consent to participate in the study. Withdrawal Criteria 1. Participants request to withdraw from the study. 2. Can not complete all sessions of the program. 3. Have health complications during the intervention, such as hypertension, gestational diabetes, preterm labor, prenatal bleeding, severe anemia, or abnormal fetal health.

Design outcomes

Primary

MeasureTime frame
Intention of Continuing Education at 6 weeks after end of the intervention Intention of Continuing Education Questionnaire

Secondary

MeasureTime frame
Self-Efficacy in Performing the Maternal Role at 6 weeks after end of the intervention Self-Efficacy in Performing the Maternal Role Questionnaire

Countries

Thailand

Contacts

Public ContactSarana Suwanruangsri

Faculty of Nursing, Prince of Songkla University

sarana.s@psu.ac.th074286556

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026