- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05021497
Effects Of Global Postural Re-Education (GPR) On Patients With Non-Specific Neck Pain.
December 12, 2024 updated by: Riphah International University
Pain is an "unpleasant sensory and emotional experience (associated with actual or potential tissue damage".
Chronic pain is a sensation of hyperalgia to muscles, ligaments and skin on both active and passive movements.
Chronic pain has a tendency to prevent people from working and exercising
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Neck pain is a very common clinical condition which equals the economic, social cost and level of disability to that of low back pain.Mechanical neck pain that occurs without an identifiable underlying disease and anatomical abnormality is termed as "non-specific" neck pain (NS-NP).Mechanical neck pain commonly arises insidiously and is generally multifactorial in origin.Two most common complains associated with chronic specific and non-specific neck pain are Kinesiophobia (fear of movement) and Postural asymmetry (forward head posture).
Medical, surgical and physical therapy treatments are recommended for addressing chronic non-specific neck pain.
Within the scope of physical therapy conventional management consist of many different techniques such as therapeutic exercises, electrotherapy, Pilates, yoga and manual therapy.
Manual therapy is among the most common used method for treating musculoskeletal conditions including chronic neck pain.
Manual therapy consists of stretching techniques, joint mobilization/manipulation, isometric/dynamic strengthening exercises and fascial manipulation or release.
Global Postural Re-education (GPR) is an alternative therapeutic strategy based on the concept that postural muscles are organized in the form of 'muscle chains' located on the anterior and posterior aspect of the spine.
It involves the global stretching of the anti-gravitational muscles and the kinetic muscle chains.
Study Type
Interventional
Enrollment (Actual)
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 Locations
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Punjab
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Islamabad, Punjab, Pakistan, 46000
- Islamabad Physiotherapy and Rehabilitation Centre (IPRC)
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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
25 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Chronic non-specific neck pain ≥ 3 months.
- No prior medication and Physical Therapy interventions from last 3 months.
- Pain: moderate level (6 on NPRS).
Exclusion Criteria:
- History of any trauma .
- History of any psychological condition.
- Specific causes of Neck Pain (e.g., systemic, rheumatic, neuromuscular diseases).
- Presence of central and peripheral neurological sign.
- Spinal surgery
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Global Positional Re-education
|
A series of gentle active movements and postures aimed at realigning joints and stretching shortened muscles.
GPR includes 8 therapeutic postures in lying, sitting and standing.
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Active Comparator: Conventional Physical Therapy Program
Conventional therapy will consist of a combination of manual techniques
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Axial traction will be given for 5 minutes, followed by mobilization of the muscle fascia along with static stretching of the scalene, levator scapulae, upper trapezius, sternocleidomastoid and pectoralis minor muscles.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric pain rating scale
Time Frame: six weeks
|
The NPRS is an 11-point numeric scale, it is the segmented numeric version of the visual analog scale.
Subjects will be asked to mark/select a whole number for 0-10 that best describes their perceived pain intensity of the last 24 hours.
Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six weeks
|
|
Neck Disability Index
Time Frame: six weeks
|
it is a 10-item self-report questionnaire that measures the patient's disability related to his/her neck pain.
It is the most commonly used questionnaire for neck disability; its reliability and validity has been demonstrated in many literatures and languages.
Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six weeks
|
|
Goniometer for Cervical Range of Motion
Time Frame: six weeks
|
The active cervical range of motion (CROM) will be measured in sitting posture by using a universal goniometer, which consists of two arms; one that is stationary and one that is moveable.
Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six weeks
|
|
Tampa Scale of Kinesiophobia
Time Frame: six weeks
|
Tampa Scale of Kinesiophobia (TSK).
TSK is a 17-items questionnaire based on the evaluation of fear of movement, fear of physical activity and fear of re-injury in patients suffering from chronic musculoskeletal pain.
It is the most widely used fear avoidance behavior questionnaire with good level of reliability and validity as documented in different literatures.
TSK is composed of 17 items with score ranging from 1to 4 for each item, ultimately having a total score ranging from 17-68.Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Forward Head Posture:
Time Frame: six weeks
|
Ruler method.
This method involves measuring the distance from the wall to the tragus of the ear (Tragus to wall test) and from wall to the posterior aspect of acromion of shoulder by a ruler in standing position.
The normal distance of Tragus to wall (TTW) in males is 10.55 cm and in females is 10.00 cm, whereas the normal distance of shoulder from wall in relaxed standing position should be less than 5 cm.Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six weeks
|
|
Global Perceived Effect Questionnaire:
Time Frame: six week
|
Perceived effect of the intervention will be assessed by using the Global Perceived Effect Questionnaire (GPE), a 5-point Likert-type scale evaluating the subjective self-reported improvement or deterioration after the intervention.
GPE is widely used in the physical therapy literature.
Assessment to be done at baseline, after 1st session, at 3rd week and at 6th week
|
six week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maria khalid, MSOMPT, 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)
February 15, 2021
Primary Completion (Actual)
July 10, 2023
Study Completion (Actual)
July 10, 2023
Study Registration Dates
First Submitted
August 23, 2021
First Submitted That Met QC Criteria
August 24, 2021
First Posted (Actual)
August 25, 2021
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 12, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/00941 Faisal Saeed
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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