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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01720004
Other study ID # IGO-103690
Secondary ID
Status Completed
Phase Phase 1
First received October 24, 2012
Last updated October 30, 2012
Start date October 2010
Est. completion date February 2012

Study information

Verified date October 2012
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Canadian Institutes of Health Research
Study type Interventional

Clinical Trial Summary

The investigators designed a pilot randomized controlled trial to assess the feasibility and acceptability of repeated hands-and-knees positioning during labour. The objectives were 1) to provide an estimate of enrollment rates, 2) to assess compliance with the study protocol by participants and care providers, 3) to obtain women's views about their experiences using the hands-and-knees position, and 4) to provide estimates of treatment effects to inform the sample size calculation for a large trial.


Description:

Women were enrolled in the pilot randomized controlled trial at two hospitals, one in Canada and one in the USA. Nurses at both hospitals were trained in how to assist women into the hands-and-knees position in bed. Repeated hands-and-knees position was defined as attempts to use the position for 15 minutes, hourly from randomization until delivery. Women were not asked to assume hands-and-knees for delivery.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- nulliparous;

- >37 weeks 0 days gestation

- in established early labour

- anticipating a vaginal delivery of a single fetus in the cephalic position

- competent to give informed consent .

Exclusion Criteria:

- delivery was anticipated within 3 hours

- a medical contraindication or physical limitation such that hands-and- knees position was contraindicated

- had a doula or midwife who encouraged the use of hands-and-knees position.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Repeated hands-and-knees positioning during labour
Details are in the Arm Description.

Locations

Country Name City State
Canada Toronto East General Hospital Toronto Ontario
United States Texas Health Harris Methodist Hospital Fort Worth Texas

Sponsors (2)

Lead Sponsor Collaborator
University of Toronto Canadian Institutes of Health Research (CIHR)

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Method of birth Spontaneous vaginal, assisted vaginal (vacuum or forceps), Caesarean at delivery No
Other pharmacologic analgesia regional analgesia or intramuscular analgesia administered during first or second stage labour Initiated during labour No
Other oxytocin during first or second stage labour any oxytocin infusion from randomization until end of second stage No
Other dislodged epidural catheter dislodged epidural catheter from randomization until delivery Yes
Other Fall Mother fell while attempting hands-and-knees position from randomization until delivery Yes
Other perineal trauma any perineal trauma (episiotomy and/or laceration0 requiring suturing at delivery No
Other maternal postpartum complications postpartum hemorrhage or complication requiring prolonged stay between delivery and hospital discharge No
Other Apgar Score Neonatal Apgar Score at one and five minutes after birth No
Other length of hospital stay length of stay for mother and baby after birth from delivery to discharge No
Other admission to neonatal intensive care unit newborn admitted to neonatal intensive care unit between birth and hospital discharge No
Other labour length Length of time between randomization and delivery from randomization until delivery No
Primary Compliance Use of hands-and-knees position for at least 15 minutes hourly during hospital labour. from randomization to delivery No
Secondary Persistent back pain Persistent back pain intensity rating measured hourly during hospital labour. hourly during labour, from randomization to delivery No
Secondary women's views women's views of their birth experiences, including satisfaction with care and care providers, views about hands-and-knees positioning, willingness to use hands-and-knees position in a subsequent labour, comparison of expectations versus experiences of labour. The measures used to assess women's views had been developed for and used in prior trials of forms of intrapartum care by Hodnett and colleagues. Most questions were Likert scales or categorical items. assessed prior to hospital discharge No
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