- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06668480
Effect of Sustained Natural Apophyseal Glide Combined With Strengthening Exercises of Lower Fibers of Trapezius in Patient With Unilateral Neck Pain
November 18, 2024 updated by: Foundation University Islamabad
Neck pain is considered one of the very common cause behind musculoskeletal pain and is 4th leading cause of disability .
Cervical pain is among 5 most contributing factors in causing years lived with disability.Individuals with unilateral neck pain exhibit significantly less Lower Trapezius strength than Middle and Upper Trapezius fibers .Mulligan is one of the mobilization techniques that can be applied in case of neck pain.In prolong neck pain there is a hyperactivation and shortening of upper trapezius which makes the lower trapezius weak this leads to imbalance between cervical and scapular muscles and result in impaired biomechanics.
So mostly treatment focused on upper trapezius and neglecting the lower trapezius and this create increase chances of recurrency of neck pain because the imbalance remains present.
So, this study aims at evaluating the effects of SNAGS combined with strengthening exercises of lower fibers of trapezius .
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
38
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
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Foundation University College of Physical Therapy
-
-
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:
- Individuals aged 18-35 years
- Both gender
- Unilateral neck pain
- Symptoms of duration more than 3 months.
- NPRS scoring of greater than or equal to 4 points.
- Neck disability index score of 20% or above.
- Manual muscle testing : grade 3
Exclusion Criteria:
- Prior cervical and thoracic spine fractures, dislocations, or surgeries, spinal osteoporosis or infection, or whiplash.
- Any trauma or localized infection in neck region
- Psychiatric diseases such as phobia/obsession and depression
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 |
|---|---|
|
Experimental: SNAGS + Conventional PT Group
Participants of this group receive conventional physical therapy.Hot pack and tens ( 10 min each)
|
It will comprise of hot pack for 10 minutes, TENs at 80-100 Hz over trapezius for 10 minutes.Strengthening of deep neck flexors
Sustained natural apophysial glides will consist of frequency: 4 sets of 3-5 repetition per session for 2 weeks
|
|
Experimental: SNAGS+Strengthening of lower fibers trapezius+Conventional PT Group
|
It will comprise of hot pack for 10 minutes, TENs at 80-100 Hz over trapezius for 10 minutes.Strengthening of deep neck flexors
Sustained natural apophysial glides will consist of frequency: 4 sets of 3-5 repetition per session for 2 weeks
Strengthening exercises of lower fibers of trapezius
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ROM
Time Frame: 2 weeks
|
Cervical ROM will be measured through CROM device
|
2 weeks
|
|
Level of Neck Disability
Time Frame: 2 weeks
|
Neck Disability Index will be used to measure level of neck disability
|
2 weeks
|
|
Muscle strength
Time Frame: 2 weeks
|
MMT for Lower fibers of trapezius
|
2 weeks
|
|
Pain intensity
Time Frame: 2 weeks
|
Pain will be measured on the basis of Numeric Pain Rating Scale score.It is rated on 0-10 scale in which 0 means no pain and 10 means the maximum possible pain
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
June 10, 2024
Primary Completion (Estimated)
December 10, 2024
Study Completion (Estimated)
December 30, 2024
Study Registration Dates
First Submitted
October 30, 2024
First Submitted That Met QC Criteria
October 30, 2024
First Posted (Actual)
October 31, 2024
Study Record Updates
Last Update Posted (Estimated)
November 20, 2024
Last Update Submitted That Met QC Criteria
November 18, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2024/45
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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