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Clinical Trials/ACTRN12614000456651
ACTRN12614000456651
Terminated
未知

Amongst pregnant women labouring at term with an uncomplicated pregnancy, does the mode of information provision (written or verbal) and the timing of information provision (36 weeks and labour, or in labour only), influence the capacity of the woman to comprehend and retain information during labour?

Royal Hospital for Women0 sites49 target enrollmentMay 1, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Informed consent during labour
Sponsor
Royal Hospital for Women
Enrollment
49
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 1, 2014
End Date
April 1, 2015
Last Updated
4 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) Adult pregnant women at 35\+0 – 36\+6 weeks of gestation at time of study enrolment
  • 2\) Normal antenatal progress
  • 3\) Baseline ability to retain information i.e. no reason to believe woman is not usually capable of giving informed consent

Exclusion Criteria

  • 1\) Requiring interpreter to give informed consent to participate
  • 2\) Major maternal or fetal pregnancy complication e.g. pre\-eclampsia, congenital abormality

Outcomes

Primary Outcomes

Not specified

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