CH1Pelvic Floor Exercises for Preventing LARS After Rectal Cancer Surgery
This study aims to see if doing pelvic floor exercises at home can prevent or reduce bowel problems in people after rectal cancer surgery.
Pelvic floor exercise
Urogenital Diseases+19
+ Low Anterior Resection Syndrome
+ Colonic Diseases
Prevention Study
Summary
Study start date: April 1, 2024
Actual date on which the first participant was enrolled.This study focuses on preventing a condition called Low Anterior Resection Syndrome (LARS) in patients who have undergone minimally invasive surgery for rectal cancer. LARS can cause problems like urgency, loss of bowel control, and constipation, significantly affecting quality of life. Pelvic floor exercises, which strengthen the muscles supporting organs in the lower body, may help prevent these issues. However, there are not many studies that confirm this benefit. The goal of this research is to explore whether these exercises can effectively reduce the risk of LARS, potentially improving the well-being of patients after surgery. Participants in the study will engage in a regimen of pelvic floor exercises following their rectal cancer surgery. The study will observe the effects of these exercises over time to determine their impact on preventing LARS. While the exercises are generally safe, the study aims to measure their effectiveness in maintaining bowel function and improving life quality for patients. The findings could lead to better recommendations for managing post-surgery complications, offering a non-invasive way to enhance recovery and prevent long-term issues.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 19 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.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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
F.D.Roosevelt University Hospital in Banská Bystrica
Banská Bystrica, SlovakiaOpen F.D.Roosevelt University Hospital in Banská Bystrica in Google Maps