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NCT02460185 Clinical Trial

Role of Maternal Physical Exercise on Spontaneous Labor Onset

Pregnancy Clinical Trial

Official title:
The Role of Maternal Physical Exercise on Spontaneous Labor Onset - A Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02460185
Other study ID # MPEX
Secondary ID
Status Completed
Phase N/A
First received May 29, 2015
Last updated October 10, 2016
Start date May 2015
Est. completion date January 2016

Study information
Verified date October 2016
Source Centro Hospitalar Lisboa Norte
Contact n/a
Is FDA regulated No
Health authority Portugal: Health Ethic Committee
Study type Interventional

Clinical Trial Summary

Evaluate the effects of the practice of maternal physical exercise on the term of pregnancy as a method to enhance spontaneous labor.

Description:

At 38 weeks low-risk pregnant women, with singleton cephalic fetus and without previous cesarean delivery, were randomized into 2 groups: a control group without maternal physical exercise practice and a study group with 30 minutes of walking, 3 times a week at 4 Km/h. Induction of labor was performed at 41 weeks

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 16 Years and older
Eligibility Inclusion Criteria:

- 38 weeks low-risk pregnant women

- singleton cephalic fetus

- without previous cesarean delivery

Exclusion Criteria:

- pathological pregnancy

- twin pregnancy

- previous cesarean section

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

  • Labour Onset and Length Abnormalities
  • Pregnancy

Intervention

Behavioral:
• Study group: Maternal Physical Exercise
Exercise: 30 minutes of walking, 3 times a week at 4 Km/h.

Locations
Country Name City State
Portugal Departamento de Obstetricia, Ginecologia e Medicina da Reprodução Lisbon

Sponsors (1)
Lead Sponsor Collaborator
Centro Hospitalar Lisboa Norte

Country where clinical trial is conducted

Portugal, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of labor induction Rate of labor induction will be analysed 41 weeks No
Secondary Gestational age on spontaneous labor onset Gestational age will be analysed on spontaneous labor onset 5 week No
Secondary Active stage duration 1 day No
Secondary Cesarean section rate 1 day No
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