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Effect of Induction Admission of Shared Decision-Making on First Time Expectant Mothers', Self-efficacy, Anxiety, Birth Outcomes and Birth Satisfaction

Effect of Induction Admission of Shared Decision-Making on First Time Expectant Mothers', Self-efficacy, Anxiety, Birth Outcomes and Birth Satisfaction

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07479524
Enrollment
130
Registered
2026-03-18
Start date
2025-10-01
Completion date
2026-06-12
Last updated
2026-03-18

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

Conditions

Labor Induction

Keywords

SDM, decision aids, labor induction

Brief summary

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.

Interventions

DEVICEdecision aid

decision aid

Sponsors

Lee Wan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. The first pregnancy and the gestation period is more than 32 weeks, the fetus is a singleton, and the fetal position is cephalad. 2. There are no obstetric complications and the fetus is normal during prenatal examination. 3. Can communicate in Mandarin and Taiwanese 4. Natural delivery is expected 5. Complete the consent form to participate in this study

Exclusion criteria

1. Those whose delivery method expected Cesarean Section 2. Early water breaker 3. Obstetric emergency 4. Newborns have abnormal conditions

Design outcomes

Primary

MeasureTime frameDescription
Childbirth Self-Efficacy InventoryFirst pregnancy and the gestation period is more than 32 weeks to 3 days postpartumThere are a total of 62 questions, and the scoring method is based on Likert 10 points.
State-Trait Anxiety Inventory; STAIFirst pregnancy and the gestation period is more than 32 weeks to 3 days postpartumThe Situational Anxiety Scale consists of 20 items; a higher score indicates a higher level of anxiety, and vice versa. This scale measures the subject's anxiety level using a 4-point scale: 1 point represents "not at all", 2 points represent "somewhat", 3 points represent "quite a bit", and 4 points represent "very much".

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026