Manual Therapy and Pelvic Floor Exercises for Women with Constipation
This study aims to assess whether manual therapy and pelvic floor exercises can improve the quality of life for women experiencing constipation.
pelvic floor exercises
+ Pelvic floor exercises and manual therapy techniques
Behavior+3
+ Constipation
+ Motor Activity
Treatment Study
Summary
Study start date: June 14, 2024
Actual date on which the first participant was enrolled.This study focuses on helping women aged 18 to 55 who experience constipation by examining how pelvic floor exercises and manual therapy can improve the strength and function of pelvic floor muscles. Constipation can be uncomfortable and challenging, and this study aims to find effective ways to enhance muscle function to ease these symptoms. By exploring these two treatment methods, the study seeks to offer better solutions for women dealing with constipation and enhance their quality of life. Participants are divided into two groups. One group performs pelvic floor exercises and diaphragmatic breathing to strengthen their muscles. The second group also receives manual therapy techniques, such as massages and specific mobilizations, in addition to the exercises. This therapy is initially provided more frequently and then reduced over time. Participants follow a six-week program, practicing exercises five days a week, with some sessions conducted online. Nutritional advice is also provided to support digestive health. The effectiveness of these interventions is evaluated through tests conducted before and after the study, comparing results to determine improvements in muscle function and constipation symptoms.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.44 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 55 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Cizre Dr Selahattin Cizrelioglu State Hospital
Şırnak, Turkey (Türkiye)Open Cizre Dr Selahattin Cizrelioglu State Hospital in Google Maps