- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05356676
Progressive Cervical Isometric Exercises Versus Scapular Stabilization Exercises in Text Neck Syndrome
Effects of Progressive Cervical Isometric Exercises Versus Scapular Stabilization Exercises on Pain, Range of Motion and Disability in Young Adults With Text Neck Syndrome: A Randomised Controlled Trail
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Punjab
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Lahore, Punjab, Pakistan, 38000
- Recruiting
- Services Hospital
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Principal Investigator:
- Osama Ijaz, MS-OMPT
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Individuals using mobile phones for more than 6-8 hours.
- Participants both male and female of age between 18 to 28 years
- Participants with neck pain (>7 weeks)
- Participants with NDI score above 15/50 (10% or higher) or
- Participants with NPRS score above 3
Exclusion Criteria:
Specific causes of neck pain (conditions with neurological involvement such as myelopathy with weakness, numbness and sensory loss, cervical disc prolapse, and cervical spinal stenosis)
- Previous neck and upper limb surgery.
- History of cervical trauma (whiplash disorder), fractures, dislocations.
- History of congenital torticollis, frequent migraine, carcinoma, acute pain and inflammation, torticollis, unstable/acute osteoarthritis, any recent fracture, vertigo, vertebrobasilar insufficiency, chronic heart disease, myocardial infarction or pregnancy
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: Isometrics
They will be treated with progressive isometric exercises added to 60 min of combined therapy (excluding scapular stabilizing exercises) treatment session at alternative 3 days/week for 8weeks
|
Isometric neck extension -individuals will be taught to place their dominant hand posterior to their head at occiput. Then, they will be told to firmly push the head backwards against that hand, and hold for five seconds and repeat 5 times. • Participants will be asked to place the right hand flat on the same side of the head. Next. they will be instructed to firmly push the head against right hand and hold for 5 seconds and repeat five times. Same exercise will be repeated with the left hand against the left side of the head as well. • Participants will be taught to place their right hand on their right cheek. Then, they will be told to rum the face against the right hand and wait for 5 seconds and repeat five times. Same exercise was repeated with the left hand on the left cheek as well. |
Experimental: Combination Therapy
They will be treated with both isometric and scapular stabilizing exercises.and
will get 60minutes of treatment sessions at alternative 3 days/week for 8weeks
|
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
NDI (Neck disability Index)
Time Frame: 3 months
|
The Neck Disability Index (NDI) is modification of the Oswestry Low Back Pain Disability Index.
It is Patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation
|
3 months
|
NPRS (Numeric Pain Rating Scale)
Time Frame: 3 months
|
The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain.
The common format is a horizontal bar or line.
Similar to the VAS, the NPRS is anchored by terms describing pain severity extremes
|
3 months
|
Goniometer
Time Frame: 3 months
|
A goniometer is an instrument that either measures an angle or allows an object to be rotated to a precise angular position
|
3 months
|
Inclinometer
Time Frame: 3 months
|
An inclinometer is a medical device used to measure the range of motion of the joint.
They are mainly used to measure the passive range of motion and allow the medical practitioner to compare the patient's relaxed position to the ability to move
|
3 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/Lhr/22/0112 Osama
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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