- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05582733
Effects of Cervical Spine Manipulation
October 12, 2022 updated by: Madeeha Shafiq, University of Lahore
Effects of Cervical Spine Manipulation on Upper Trapezius Active Versus Conventional Techniques.
To determine the immediate effects of cervical spine manipulation on pressure pain sensitivity on upper trapezius trigger point.
it was a randomized control trial including 66 patients at physiotherapy OPD of railway rehabilitation center from August 2019 to December 2019, Railway General Hospital Pakistan and Max Rehab and decompression center Max health Hospital G8 Islamabad.
The subjects were randomly divided into two groups (group control and experimental) by free envelope method.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
To determine the immediate effects of cervical spine manipulation on pressure pain sensitivity on upper trapezius trigger point and neck ranges of motion.
A randomized control trial of 66 patients was conducted from August 2019 to December 2019 at physiotherapy OPD of railway rehabilitation center, Railway General Hospital Pakistan and Max Rehab and decompression center Maxhealth Hospital G8 Islamabad.
The subjects were randomly divided into two groups (group control and experimental) by free envelope method.
Control was treated with Manual Pressure release followed by stretching while in experimental received cervical spine manipulation (chin hold) kaltenborn followed by stretching.
Structural questionnaire was used for pre and post assessment.
Outcomes were measured by algometry and inclinometer before and after the application of respective techniques.
The data was analyzed at baseline and immediately after the intervention on IBM SPSS-21.
Study Type
Interventional
Enrollment (Actual)
66
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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Islamabad, Pakistan, 00430
- Dr. Abdul Gaffoor
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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
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 1.presence MTrps in upper trapezius
- limited side bending and rotation
- both gender
- age between 25 to 45
Exclusion Criteria:
- Malignancy, infection, trauma, bone deformities.
- Acute Disc Protrusion
- Positive VBI
- Positive Sharp purser test
- History of whiplash injury
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: CROSSOVER
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Cervical spine manipulation
In spinal manipulation, the velocity, magnitude and direction of the impulse are controlled to encourage relaxation and comfort of muscle and connective tissue.
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hot pack for 10 minutes will be applied followed by cervical manipulation (chin hold kaltenborn) once and then stretching
Hot pack will be applied followed by sustained pressure or MPR for 90 sec and then stretching.
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EXPERIMENTAL: traction
aimed to relieve pressure on the spine
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hot pack for 10 minutes will be applied followed by cervical manipulation (chin hold kaltenborn) once and then stretching
Hot pack will be applied followed by sustained pressure or MPR for 90 sec and then stretching.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
changes from the baseline in Algometer values
Time Frame: Baseline and 3 weeks
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It is a device used to identify the pressure and force eliciting a pressure pain threshold.
The hand held algometer 1 cm round rubber surface which applies force and display for readings in newtons or kilograms.Sustained force is usually applied at the right angle to the soft tissue.
Estimated pressure application rates have ranged from 0.05 to 20N/s. it has a high validity and reliability for measuring pain pressure threshold in patients of myofascial trigger points.
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Baseline and 3 weeks
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changes from the baseline in Inclinometer values
Time Frame: Baseline and 3 weeks
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It is a device used to measure neck ranges of motion.
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Baseline and 3 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Abdul Ghafoor Sajjad, PHD*, ghafoor.sajjad@riphah.edu.pk
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)
August 1, 2019
Primary Completion (ACTUAL)
December 30, 2019
Study Completion (ACTUAL)
January 28, 2020
Study Registration Dates
First Submitted
October 3, 2022
First Submitted That Met QC Criteria
October 12, 2022
First Posted (ACTUAL)
October 17, 2022
Study Record Updates
Last Update Posted (ACTUAL)
October 17, 2022
Last Update Submitted That Met QC Criteria
October 12, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC:00570
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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