A1 Pulley Stretching and Tendon Gliding Exercises for Post-operative Trigger Finger Patients: Impact on Pain, Range of Motion, and Hand Grip Strength
This study aims to evaluate the impact of A1 pulley stretching and tendon gliding exercises on pain, range of motion, and hand grip strength in patients recovering from trigger finger surgery.
A1 pulley stretching
+ Tendon Gliding exercises
+ Standard physiotherapy treatment
Muscular Diseases+2
+ Musculoskeletal Diseases
+ Tendinopathy
Treatment Study
Summary
Study start date: January 13, 2025
Actual date on which the first participant was enrolled.This study focuses on individuals who have undergone surgery for trigger finger, a condition that causes pain and stiffness in the fingers or thumb. The main goal is to understand how a combination of A1 pulley stretching and tendon gliding exercises can impact pain, flexibility, and hand grip strength in these patients. The importance of this study lies in its potential to improve rehabilitation strategies for post-operative trigger finger patients, helping them regain normal hand function more effectively. Participants in this study will engage in A1 pulley stretching and tendon gliding exercises. The effectiveness of these exercises will be measured using three tools: a hand dynamometer to assess hand grip strength, a Numeric Pain Rating Scale to evaluate pain levels, and a universal goniometer to gauge the range of motion in the affected finger. These measurements will provide insights into the recovery progress of the patients, helping to determine the benefits and potential drawbacks of the combined exercise regimen.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 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 36 to 60 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
ExperimentalGroup II
Active ComparatorStudy 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
District Headquarters Hospital
Toba Tek Singh, PakistanOpen District Headquarters Hospital in Google Maps