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NCT07479524
Effect of Induction Admission of Shared Decision-Making on First Time Expectant Mothers', Self-efficacy, Anxiety, Birth Outcomes and Birth Satisfaction
NA trial testing decision aid in Labor Induction in 130 participants. Enrolling by invitation.
12 June 2026
Quick facts
| Lead sponsor | Lee Wan |
|---|---|
| Phase | NA |
| Status | ENROLLING BY INVITATION |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | other |
| Enrollment | 130 |
| Start date | 1 October 2025 |
| Primary completion | 12 June 2026 |
| Estimated completion | 12 June 2026 |
| Sites | 1 location across Taiwan |
Drugs / interventions tested
- decision aid
Conditions studied
- Labor Induction — all drugs for Labor Induction →
Sponsor
Lee Wan
Who can join
Adults 18 to 45, female only, with Labor Induction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Women's childbirth is regarded as a natural, normal and healthy process, and no interventional measures are required unless medically necessary. However, the proportion of routine induction of labor among Taiwanese women is currently on the rise. This study intends to use the medical-patient shared decision-making program for induction of labor to explore the impact of this program on the delivery efficiency, anxiety, delivery results, and delivery satisfaction of first-time pregnant women. In addition, we also want to explore the feelings and thoughts of this group of women who underwent induced labor under the Shared Medical Decision-Making Program in the postpartum period after participating in this program. It can be used as an improvement reference for the future implementation of shared decision-making between doctors and clients. This research adopts a qualitative and quantitative mixed research method to conduct this research. The quantitative research will adopt an experimental research design. Those who meet the criteria will be randomly assigned to collect the experimental group and the control group. In addition to receiving general routine care, the experimental group also receive a shared decision-making plan for delaying admission to the hospital. The control group received regular care. The results of measurement include knowledge about birth scale, anxiety scale, birth outcomes and birth satisfaction scale. The qualitative study is the application of one-to-one and in-depth interviews and semi-structured interview guidelines will be used to collect data, and the application of content analysis to analyze the data.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07479524
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Related trials
Other trials of decision aid
Trials testing the same drug.
- NCT04034979 — Evaluation of a Decision Aid About Life-sustaining Therapies · NA · completed
- NCT02644382 — Improving Surgical Decision-making in Young Women With Breast Cancer · completed
Other recruiting trials for Labor Induction
Currently open trials in the same condition.
- NCT07006896 — Induction of Labor After Cesarean Using Foley Alone vs. Concurrent Foley and Oxytocin · NA · recruiting
- NCT07109258 — Effect of Dexamethasone on Labour Induction in Term Pregnancies · EARLY_PHASE1 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07479524 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Lee Wan
- Last refreshed: 18 March 2026
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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing