Reformer Pilates vs Conventional Physiotherapy for Lumbar Disc Herniation
Exercise
Agnosia+11
+ Bone Diseases
+ Fatigue
Treatment Study
Summary
Study start date: January 8, 2024
Actual date on which the first participant was enrolled.This study aims to compare the effectiveness of two different rehabilitation methods for people with lumbar disc herniation: Reformer Pilates and Conventional Physiotherapy. Lumbar disc herniation can cause significant back pain and discomfort, impacting daily activities and quality of life. By determining which method is more effective in managing pain and other symptoms like fatigue and anxiety, the study seeks to improve treatment approaches for those suffering from this condition, ultimately enhancing their overall well-being. Participants in the study followed a rehabilitation program for six weeks. Those in the Reformer Pilates group attended 12 Pilates sessions, each lasting 45-50 minutes, twice a week. Meanwhile, the Conventional Physiotherapy group completed 30 sessions, five days a week, with each session also lasting 45-50 minutes. The study measured outcomes using various questionnaires to assess pain, fatigue, sleep quality, anxiety, fear of movement, and overall quality of life, both before and after the treatment. Results showed that Reformer Pilates was particularly effective for reducing pain, while Conventional Physiotherapy excelled in managing fatigue. Both methods proved beneficial for addressing fear of movement and fatigue, indicating the importance of choosing the right therapy based on individual patient needs.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 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.Any sex
Biological sex of participants that are eligible to enroll.From 21 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers not 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
ExperimentalStudy Objectives
Primary 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