- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06686290
Effects of Post-Isometric Relaxation Versus Static Stretching in Patients With Levator Scapulae Syndrome.
November 12, 2024 updated by: Riphah International University
Effects of Post-Isometric Relaxation Versus Static Stretching on Pain, Range of Motion, Disability and Muscle Length in Patients With Levator Scapulae Syndrome.
Group A will be treated with Postisometric relaxation technique and Group B will be treated with Static stretching technique.
Postisometric relaxation will be performed with the frequency of 5 times, such that it includes (30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold.
Stretching exercise will be performed with 30 second hold and with 5 repetitions.
All Exercises will be performed 3 times per week for total of 4 weeks.
Outcome measures will be conducted through pain, range of motion, disability and muscle length after 4 weeks.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
A Randomized Clinical Trial will be conducted at Tehsil Head Quarter Hospital Daska through consecutive sampling technique on 42 patients which will be allocated using computer generated sampling (random number table) into Group A and Group B. Group A will be treated with Postisometric relaxation technique and Group B will be treated with Static stretching technique.
Postisometric relaxation will be performed with the frequency of 5 times, such that it includes (30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold.
Stretching exercise will be performed with 30 second hold and with 5 repetitions.
All Exercises will be performed 3 times per week for total of 4 weeks.
Outcome measures will be conducted through pain, range of motion, disability and muscle length after 4 weeks.
Data will be analyzed during SPSS software version 25.
The normality of data will be assessed by Shapiro-wilk test after which it will be decided either parametric or non-parametric test will be used within a group or between two groups.
Study Type
Interventional
Enrollment (Estimated)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Imran Amjad, Phd PT
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Daska, Punjab, Pakistan
- Recruiting
- Tehsil Headquarter Hospital Daska
-
Contact:
- Ali Raza, DPT
- Phone Number: 03326099065
- Email: ali.raza65@gmail.com
-
Principal Investigator:
- Aiman Tariq, DPT
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Both males and females.
- Age range of 24-59 years.
- Neck and medial border scapular pain for at least 3 months.
- NPRS score greater than 3.
- Reduced side flexion and rotation of neck.
- Symptoms persisted for at least 3 months.
- Positive levator scapulae length test.
- Have suffered from myofascial pain
Exclusion Criteria:
- Neuropathies.
- Vertebral fractures.
- Pregnancy.
- Fibromyalgia.
- Cancer.
- Traumatic neck injury.
- Previous cognitive and functional disorders.
- Coagulopathy(
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Post Isometric Relaxation Technique
Postisometric relaxation will be performed with the frequency of 5 times, such that it includes 30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold.
|
Post isometric relaxation will be performed with the frequency of 5 times, such that it includes 30 isometric contraction of the muscle to be stretched for 10 seconds, followed by rest period of 5 seconds and then a stretch of 10 seconds hold.
|
|
Experimental: Static Stretching
Stretching exercise will be performed with 30 second hold and with 5 repetitions.
All Exercises will be performed 3 times per week for total of 4 weeks.
|
Static Stretching
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Level
Time Frame: Pre & Post 6 weeks
|
Numeric Pain Rating Scale
|
Pre & Post 6 weeks
|
|
Disability Level
Time Frame: Pre & Post 6 weeks
|
Neck Disability Index
|
Pre & Post 6 weeks
|
|
Range of Motion
Time Frame: Pre & Post 6 weeks
|
Goniometer
|
Pre & Post 6 weeks
|
|
Muscle Length
Time Frame: Pre & Post 6 weeks
|
Levator Scapulae Index
|
Pre & Post 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Muhammad Hassan, MSPT, Riphah International University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 24, 2024
Primary Completion (Estimated)
January 24, 2025
Study Completion (Estimated)
February 24, 2025
Study Registration Dates
First Submitted
November 12, 2024
First Submitted That Met QC Criteria
November 12, 2024
First Posted (Estimated)
November 13, 2024
Study Record Updates
Last Update Posted (Estimated)
November 13, 2024
Last Update Submitted That Met QC Criteria
November 12, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/24/0117
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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