Skip to content

Induction of Women With Fear of Labor

Planned Induction of Women With Fear of Labor and Evaluation of the Experience of Delivery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01424059
Enrollment
250
Registered
2011-08-26
Start date
2011-01-31
Completion date
2013-12-31
Last updated
2011-08-26

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

Conditions

Fear

Keywords

fear, labor, induction, amniotomy, WEDQ-B, parous, cesarean section

Brief summary

The purpose of this study is to evaluate the experience of labor in parous women induced because of fear of labor and, to compare the experience of parous women induced without fear of labor. A comparison with the experience of women delivered with elective cesarean section because of fear of labor is done. In the induced labors, the induction method is amniotomy. Between groups the experience of delivery is evaluated with a questionnaire: Wijma Delivery Expectancy Questionnaire(WEDQ-B). Groups are also compared with regard to time from induction to delivery and rate of operative delivery. Hypotheses: * there is no difference in experience of delivery * there is no difference in time to delivery or rate of operative deliveries

Interventions

OTHERWEDQ-B (questionnaire)

Questionnaires are answered after delivery; within 48 hours and after five weeks

Sponsors

Uppsala University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* parous * induction or cesarean section * amniotomy

Exclusion criteria

* non proficiency in the Swedish language

Design outcomes

Primary

MeasureTime frameDescription
experience of deliveryWithin 48 hours after deliveryExperience of labor is evaluated with a questionnaire (WEDQ-B) within 48 hours

Secondary

MeasureTime frameDescription
Operative deliverywithin 48 hourswithin 48 hours from inclusion in the study

Countries

Sweden

Outcome results

None listed

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