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Clinical Trials/NCT01424059
NCT01424059
Unknown
Not Applicable

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

Uppsala University Hospital1 site in 1 country250 target enrollmentJanuary 2011
ConditionsFear

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fear
Sponsor
Uppsala University Hospital
Enrollment
250
Locations
1
Primary Endpoint
experience of delivery
Last Updated
14 years ago

Overview

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
Registry
clinicaltrials.gov
Start Date
January 2011
End Date
December 2013
Last Updated
14 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maria Jonsson

M.D., Ph.D. Consultant

Uppsala University Hospital

Eligibility Criteria

Inclusion Criteria

  • induction or cesarean section
  • amniotomy

Exclusion Criteria

  • non proficiency in the Swedish language

Outcomes

Primary Outcomes

experience of delivery

Time Frame: Within 48 hours after delivery

Experience of labor is evaluated with a questionnaire (WEDQ-B) within 48 hours

Secondary Outcomes

  • Operative delivery(within 48 hours)

Study Sites (1)

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