Clinical trial Recruiting at 1 site Interventional Ages 20 and up

Multimedia childbirth prediction for first-time mothers and their partners

Official title: Department of Nurse-Midwifery and Women Health Graduate Institute of Nurse Midwifery

Run by Mackay Memorial Hospital · NCT06816186 · Data updated 2026-11-12

This project tests whether a multimedia program for first-time, low-risk mothers and their partners can reduce hospital visits, lower anxiety, and increase confidence near term.

Quick facts

Study typeInterventional
Ages20 Years and up
SexAll
Enrollment190 (estimated)
SponsorMackay Memorial Hospital
Academic / other
Locations1 site (Hsinchu, Hsinchu)
StatusRecruiting
StartedFebruary 3, 2024
Main results expectedAugust 31, 2025
Study endsAugust 31, 2025
Registry record updatedAugust 15, 2025
Trial IDNCT06816186 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are first-time, low-risk pregnant women over age 20 with a single cephalic fetus between 37 and <40 weeks and their spouses who can read, speak, and write Chinese.

Probably not a fit

People with diagnosed prenatal mental illness, fetuses requiring admission to higher-level care (moderate/severe ward or NICU), multiple pregnancies, non-cephalic presentation, planned cesarean delivery, or inability to read/speak Chinese are unlikely to benefit.

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

What this trial studies

This quasi-experimental trial enrolled 95 couples of first-time, low-risk pregnant women and their spouses and assigned them to a multimedia intervention or usual care. The multimedia program provided information about birth signs and coping strategies, and outcomes measured included number of hospital visits, situational anxiety (STAI-S), and a self-confidence visual analog scale. Data were collected at 37 weeks' gestation, at the first hospital visit, and one hour after admission for delivery. Analyses used t tests, chi-square, ANOVA, generalized estimating equations, and linear regression to compare groups.

Why it matters

Potential benefit: If successful, the program could reduce unnecessary hospital trips, decrease maternal anxiety, and boost confidence during labor for first-time low-risk pregnancies.

How similar studies have gone: Prior prenatal education programs have generally reduced childbirth-related fear and anxiety, so similar multimedia approaches have supporting evidence, though this specific prediction intervention is not widely tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
1. Low-risk first-time mothers over 20 years old and their spouses
2. Pregnancy \>37 weeks, pregnancy \<40 weeks
3. Single birth, head position
4. Vaginal producers
5. Those who can listen, speak, read and write Chinese

4\. Diagnosed by a doctor as prenatal mental illness 5. The fetus' condition requires admission to a moderate or severe ward or intensive care unit.

Where it's running

  • Mackay Memorial Hospital
    Hsinchu, Hsinchu, Taiwan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.