Clinical Trials Directory

Trials / Completed

CompletedNCT04431102

Pilates and the Pelvic Floor: A Quasi-experimental Study

The Effects of the Pilates Method on Pelvic Floor Injuries During Pregnancy and Childbirth: A Quasi-experimental Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
University of Huelva · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

In this paper, it is postulates that in pregnant women, the practice of PM led by a qualified professional for a period of four weeks can reduce the incidence of pelvic floor dysfunction (PFD) by decreasing the number of birth injuries.

Detailed description

It is postulated that in pregnang women, the practice of PM can reduce the severity of birth injuries. Our main objective was to determine the effectiveness of a PM program to reduce the incidence and degree of intrapartum perineal injuries as a way to reduce the incidence of female PFD. Secondary objectives were: Assess the role of a MP program on the systolic and diastolic blood pressure. Determine the effect of a MP program on body weight (BMI). It is a parallel group clinical trial with an allocation ratio of 1:2. All pregnant women will be informed about the nature of the clinical trial. There will be no differences in the pregnant´s follow-up because it will be performed by two same Pilates monitor with the same formation. Once the pregnant women is assigned to an arm of the study, those assigned to the intervention group will be sent to the Pilates monitor to explain and initiate the exercise of MP program while the control group will be informed to maintain their usual monitoring of pregnancy. In the initial visit, the type of physical activity will be evaluated by filling in the international physical activity questionnaire (IPAQ).

Conditions

Interventions

TypeNameDescription
OTHERPILATES METHODIt is intended that the Pilates program have a duration of four weeks and its realization does not suppose an excessive consumption of resources. Therefore, it must have a series of characteristics: low supervision and easily realizable by all patients, which implies flexibility in the schedule. In this sense the sessions of Pilates is adjusted to these assumptions and the Pilates monitor offers several schedules on diferent days of week. The pregnant women assigned to the intervention group will be supervised by the midwifery of reference and trained by a Pilates monitor who will explain the training program and resolve the doubts raised by the women. The therapeutic control will be carried out by telephone call and clinical history review between the eighth and tenth day.

Timeline

Start date
2018-11-05
Primary completion
2019-07-31
Completion
2019-12-27
First posted
2020-06-16
Last updated
2020-06-17

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04431102. Inclusion in this directory is not an endorsement.