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Maternal Informing on Labor Induction: Impact on Childbirth Experience

Maternal Informing on Labor Induction: Impact on Childbirth Experience

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07272785
Enrollment
50
Registered
2025-12-09
Start date
2025-12-08
Completion date
2026-06-30
Last updated
2025-12-23

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

Conditions

Childbirth Experience, Humans, Labor, Induced, Labor, Obstetric, Pregnancy, Prospective Study, Prospective Study , Questionaires

Keywords

Childbirth experience, Induction of labor, Pregnancy, Childbirth, Obstetrics

Brief summary

The aim of this study is to explore the information provided to mothers about labor induction and its connection to their childbirth experience. In addition, the study examines how the use of social media may influence the birth experience among patients undergoing labor induction.

Detailed description

Subject undergoing planned induction of labor will be recruited. At recruitment the participants will be asked to answer a questionnaire. Follow-up questionnaires will be sent to the participants one week and three months after the induction. The first questionnaire assesses how well the participants were informed about the induction. The following questionnaires will assess the childbirth experience and induction experience. The main aim of the study is to investigate whether being being well informed about the induction of labor is related to better experience of childbirth. Moreover, the correlation between reported social media use and childbirth experience will be evaluated. After obtaining full data from the first 50 subjects an interim analysis will be performed, to decide the final target sample size.

Interventions

None listed

Sponsors

Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned induction of labor at the antenatal ward or at the outpatient clinic * Adequate language skills (Finnish, Swedish, English)

Exclusion criteria

* Induction at the delivery ward or at the obstetric emergency care clinic * Spontaneous onset of labor or a planned cesarean delivery * Age below 18 years at the time of recruitment

Design outcomes

Primary

MeasureTime frameDescription
Childbirth experienceThree months after induction of laborChildbirth experience assessed using visual analog scale (VAS) where 0 is the worst possible and 10 the best possible childbirth experience.

Secondary

MeasureTime frameDescription
Childbirth experienceOne week after induction of laborChildbirth experience assessed using visual analog scale (VAS) where 0 is the worst possible and 10 the best possible childbirth experience.
Experience of labor inductionOne week after induction of laborAssessed using visual analog scale (VAS) where 0 is the worst possible and 10 the best possible labor induction experience.
Did childbirth experience meet participant's expectationsOne week after induction of laborFour points Likert scale with the following possible answers: 1) very poorly, 2) quite poorly, 3) quite well, 4) very well.

Countries

Finland

Contacts

Primary ContactMikael Huhtala, M.D., Ph.D.
misahu@utu.fi+35823130000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026