- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06028958
Global Postural Re-Education And Neck Isometric Exercises In Cervical Radiculopathy RADICULOPATHY
March 27, 2025 updated by: University of Lahore
Effects Of Global Postural Re-Education And Neck Isometric Exercises In Patients With Cervical Radiculopathy
Cervical radiculopathy is a common neurological disorder that is caused by compression of the nerve, inflammation of nerve roots, or space-occupying lesions.
Cervical radiculopathy is the most common health-related problem worldwide.
The conservative approach like education, specific exercises, and spinal manipulation is usually given for chronic cases with good outcomes.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Cervical Radiculopathy is a condition in which a nerve is entrapped between the bones and causes numbness and tingling.
Neck isometric exercises are a basic treatment plan for strength training.
Global postural reeducation is a technique the manual cervical traction along with body alignment that helps to reduce symptoms more rapidly.
This whole procedure is completed more easily, without a machine and satisfying for the patient.
Study Type
Interventional
Enrollment (Actual)
85
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 Locations
-
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Punjab
-
Lahore, Punjab, Pakistan, 5400
- The University of Lahore
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-
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:
- 18 to 35 years.
- Both genders, Males and females
- One-sided upper limb pain or numbness
- Any 2 out of 4 tests are positive Spurling test, Distraction test, Ipsilateral cervical traction test, and Upper Limb test
Exclusion Criteria:
- Bilateral upper limb pain
- Previous history of cervical surgery
- Cervical spine
- Injection therapy in the past 2 weeks
- Being Pregnant women
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Neck Isometrics Exercises
This group of participants will receive neck isometric exercises along with routine physical therapy and a hot pack.
In this regimen, the patient is commanded to apply minimal resistance on the physiotherapist's hand in front, back, and lateral positions.
This resistance is applied for 10 sec with a 15 sec hold with 10-15 repetitions.
The protocol will be given to the participants for two weeks.
Each session will be of 40 minutes.
|
Isometric exercises are tightening (contractions) of a specific muscle or group of muscles.
During isometric exercises, the muscle doesn't noticeably change length.
The affected joint also doesn't move.
Isometric exercises help maintain strength.
|
|
Experimental: Global Posture Re-Education
This group of participants will receive the Global Posture Re-Education technique with a hot pack.
The protocol will be given to the participants for two weeks (1 session on an alternative day with the home plan).
Each session will be of 40 minutes.
|
Global postural rehabilitation (GPR) is an approach that considers the body in its overall aspect.
This technique aims to relax the envelope of the muscles (fascia) while relaxing the muscle chains to reduce the strain on the joints.
The end result is a more suitable posture and less pain.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: Pain intensity will be measured at baseline, and change in pain intensity will be measured at 1st week, and 2nd week of treatment..
|
Neck pain will be assessed utilizing the 10cm Visual Analogue Scale.
The members will register their current pain level by selecting any from 0(no pain) to 10(unbearable pain) presented ahead a level line.
|
Pain intensity will be measured at baseline, and change in pain intensity will be measured at 1st week, and 2nd week of treatment..
|
|
Level of Functional Disability
Time Frame: Change in Functional Status will be measured at baseline, at first week, and at second week of treatment.
|
The level of Functional disability will be measured by using the neck disability index.
It contains 10 readings including pain intensity, personal care, headache, lifting, reading, concentration, work, driving sleeping, and recreation.
The questions are measured on a 6-point scale from 0 (no disability) to 5 (full disability).
The numeric response for each item is summed for a score varying from 0 to 50.
|
Change in Functional Status will be measured at baseline, at first week, and at second week of treatment.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ashfaq Dr Ahmed, PhD, The University of Lahore
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)
July 1, 2023
Primary Completion (Actual)
October 1, 2023
Study Completion (Actual)
October 15, 2023
Study Registration Dates
First Submitted
August 31, 2023
First Submitted That Met QC Criteria
August 31, 2023
First Posted (Actual)
September 8, 2023
Study Record Updates
Last Update Posted (Actual)
March 28, 2025
Last Update Submitted That Met QC Criteria
March 27, 2025
Last Verified
August 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-UOL-487-08-2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Time Frame
It will be shared soon after publication
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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