- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05070559
Active Release Technique and Graston Technique in Patients With Lateral Epicondylitis
Comparison of Active Release Technique and Graston Technique In Patients With Chronic Lateral Epicondylitis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 44000
- Rawal General Hospital Rawalpindi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Chronic lateral epicondylitis, complaints for at least 3 months or more
- Pain intensity level between 3 to 6 on 0-10 point numerical pain rating scale
Exclusion Criteria:
- Acute/ sub-acute lateral epicondylitis
- Any cervical spine or any other upper limb dysfunction
- Any other neurological disease, cardiovascular disease, osteoporosis
- Bilateral complaints
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Active Release Technique Group
Patients in this group will receive Active Release Technique along with conventional therapy
|
Patients in this group will receive Active Release Technique along with conventional therapy. ART will be given with patient seated, elbow flexed and resting on the treatment table, forearm in midprone & wrist in neutral position and then the therapist will work on the common extensor tendon by applying pressure to the tendon distal to their attachment at the elbow. The patient will start with the elbow bent and wrist straight. As the therapist hold the muscles, the patient will extend the elbow and pronate and flex the wrist while the therapist move the pressure proximally, attempting to release adhesions around and between muscle planes. Total of 15 repetitions for of 10 minutes. CONVENTIONAL THERAPY:
|
|
Experimental: Graston Technique Group
Patients in this group will receive Instrumental Assisted Soft Tissue Mobilization along with conventional therapy
|
Patients in this group will receive IASTM along with conventional therapy. In graston technique proper application of GT3 which include application of a cream to the common extensor tendon. The GT3will be then used to common extensor tendon. In areas of increased tissue restriction, more required pressure with GT3 is applied using increased force and shorter strokes over the areas of restriction. Ice will be offered as needed for pain management after each session. The study includes interventional protocol of 4 weeks. The sessions will be given 3 times a week for 4 weeks. CONVENTIONAL THERAPY:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: 4 Weeks
|
The Numeric Pain Rating Scale that is a unidimensional measure of pain intensity in adults.
The 11-point numeric scale ranges from '0' representing one pain extreme (no pain) to '10' representing the other pain extreme (or "worst pain imaginable").
The intrarater reliability with ICC = 0.67.
|
4 Weeks
|
|
Hand Dynamometer
Time Frame: 4 Weeks
|
hand dynamometer is the most reliable and acceptable tool for measuring grip strength.
It detects and quantitatively determines the degree of weak grip strength.
(ICC = 0.99)
|
4 Weeks
|
|
Patient-Rated Tennis Elbow Evaluation
Time Frame: 4 Weeks
|
The Patient-Rated Tennis Elbow Evaluation questionnaire is a specific questionnaire available for assessing the functional status of patients with lateral epicondylitis.
(ICC = 0.96)
|
4 Weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sajjad Ali, Ms-OMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Iqra Shabbir
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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