Pregnancy Clinical Trial
Official title:
The Effects of the Pilates Method on Pelvic Floor Injuries During Pregnancy and Childbirth: A Quasi-experimental Study
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.
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).
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