- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05834114
Mckenzie and Rhythmical Stabilization Technique on Chronic Neck Pain
The Effects of Mckenzie Protocol Versus Rhythmic Stabilization Technique on Pain, Range of Motion and Disability in Chronic Neck Pain.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Neck pain is a very common ailment that results in a great deal of suffering, impairment, and financial expense. The International Association for the Study of Pain is defined as Pain perceived as arising from anywhere within the region bounded superiorly by superior nuchal line, inferior by an unoriginally transverse line through the tip of first thoracic spinous process, and laterally by sagittal plane tangential to the lateral border of neck. According to the study's findings, 69% of Balochistan University undergraduate students in Quetta, Pakistan, experienced neck pain. Pain in many cervical spine structures has the potential to become chronic neck pain. In epidemiologic research, pain is considered chronic if it lasts more than three months to six months, or five years.
McKenzie's treatment regimens were first used in Sweden in 1985 to address mechanical spine patient issues. For these kinds of patients, protocols were often employed in the 1990s. Repeated neck retraction exercises considerably lessen the pain and restore the cervical spine's lordosis curve in individuals with spinal pain.
Rhythmic Stabilization is characterized by isometric contractions against the resistance provided by the therapist, with the subject trying to maintain their position as the therapist changes the direction of resistance. Both techniques are effective in pain and range of motion in chronic neck pain.
McKenzie protocol and rhythmic stabilization are both studied individually before but their effects are not compared previously.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Lahore, Punjab, Pakistan
- Ghurki Trust Teaching Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 30-50
- Localized chronic neck pain for more than 3 months.
Exclusion Criteria:
- Participants suffering their neck pain was caused by any other complications.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: McKenzie protocol
In this group, 20 participants will be included.
the interventions will be given for 15 mint.
The exercises then repeated five or six times in a Session.
the session will be of 45 mins, 3 session per week.
|
In this group 20 participants will receive McKenzie protocol with conventional physical therapy.
Participants will be asked to sit to treat extension deficit.
The participant will be in a comfortable sitting position with a proper back support.
Head is kept in forward facing without any up and done movement (10 to 15 times).
Then, he restored the neutral sitting posture, and at the end of the range of motion (ROM), he' tuck in" chin by pushing the chin with his fingers (10 to 15 times).
Subsequently, the participant will be requested to return to the original position while the therapist one hand's forefinger placed alongside the participant's mandible (to stabilize the head at full retraction position), and the heel of the other hand placed on the first or second dorsal vertebra (to provide posterior-anterior force).
The exercises then repeated five or six times in a Session.
the session will be of 45 mins, 3 session per week.
Other Names:
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Active Comparator: Rhythmic stabilization technique
In this group, 20 participants will be included.
Rhythmic Stabilization with traditional physical therapy will be given for 3 sessions of 45 minutes a week, over a period of 10 weeks.
|
In this group participants will receive Rhythmic stabilization, with Conventional physiotherapy treatment the flexion , extension exercises performed.
During flexion pattern the experimenter stood at the right side of patient and used his tip of fingers at chin.
The experimenter then put his left hand at anterior side of head to apply resistance.
then extension pattern is resisted and asked patient to match my resistance.
The experimenter provided resistance against right rotation and lateral flexion provided during the exercise in order to induce strong muscle contractions.
3 sessions of 45 minutes a week, over a period of 10 weeks.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric pain rating scale for pain
Time Frame: 3 weeks
|
NPRS is based on 11-point numerical rating scale for determining pain intensity, 0(no pain) to 10(worst pain imaginable) pain intensity.
On average over the past 2 day how bad has your pain been.
|
3 weeks
|
|
Neck disability index
Time Frame: 3 weeks
|
The Neck Disability Index (NDI) (modification of the Oswestry Low Back Pain Disability Index). (0-8%) no disability, ( 10 - 28%) mild disability, (30-48% ) moderate disability, (50- 64%) severe disability, (70-100%) complete disability |
3 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Universal goniometer
Time Frame: 3 weeks
|
It is used to measure ranges of neck flexion, extension, lateral rotation(right, left), Side bending (right, left)
|
3 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Sanaullah, MS, Study Principal Investigator
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/23/0108 Mustajab
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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