A randomised controlled trial of the effect of ambulation in the first stage of labour in terms of duration of labour of women with a previous caesarean

ISRCTN ISRCTN41730576
DOI https://doi.org/10.1186/ISRCTN41730576
Secondary identifying numbers N0170149149
Submission date
30/09/2005
Registration date
30/09/2005
Last edited
16/10/2015
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Pregnancy and Childbirth
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Ms C McCormick
Scientific

Nottingham City Hospital
Nottingham
NG5 1PB
United Kingdom

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeNot Specified
Participant information sheet Not available in web format, please use the contact details below to request a patient information sheet
Scientific titleA randomised controlled trial of the effect of ambulation in the first stage of labour in terms of duration of labour of women with a previous caesarean
Study objectivesWill ambulation during labour shorten the first stage of labour in women who have previously undergone one previous caesarian?
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedPregnancy and Childbirth: Labour
Intervention1. Encourage walking/mobilisation
2. Walk/mobilise as little/much as desired
Intervention typeOther
Primary outcome measureDuration of labour in each group
Secondary outcome measuresNot provided at time of registration
Overall study start date20/07/2004
Completion date31/07/2006

Eligibility

Participant type(s)Patient
Age groupAdult
SexFemale
Target number of participants200
Key inclusion criteria200 women in latter stages of pregnancy
Key exclusion criteria1. Women who intend to have a second planned elective caesarian section
2. Women who do not understand/speak English well enough to give valid consent
3. Non-cephalic presentation; known fetal abnormality
4. More than one previous LSCS; previous classical, inverted T or J incision to the uterus
5. Multiple pregnancy
6. Pre-term labour 37 weeks
8. Induced labour
Date of first enrolment20/07/2004
Date of final enrolment31/07/2006

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Nottingham City Hospital
Nottingham
NG5 1PB
United Kingdom

Sponsor information

Department of Health
Government

Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom

Phone +44 (0)20 7307 2622
Email dhmail@doh.gsi.org.uk
Website http://www.dh.gov.uk/Home/fs/en

Funders

Funder type

Government

Nottingham City Hospital NHS Trust (UK), NHS R&D Support Funding

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan