- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06340113
Mulligan and Mckenzie Exercises Alongwith Stabilization Exercises in Patients With Chronic Neck Pain
Comparison of Mulligan and McKenzie Exercises Along With Stabilization Exercises on Pain, Range of Motion and Disability in Patients With Chronic Neck Pain
The goal of this [type of study: Randomized control trial] is to [ compare the effectiveness of Mulligan and McKenzie Exercises along with stabilization exercises on pain, range of motion and disability ] in [ in patients with chronic neck pain].The main question it aims to answer is:
- Wether Mulligan is more effective or Mckenzie exercises along with stabilization exercises in the treatment of patients with chronic neck pain Group 1 will recieve Mulligan and stabilization exercises Group 2 will recieve Mckenzie and stabilization exercises
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Chronic neck pain is a prevalent and multifaceted condition, affecting a substantial portion of the general population (16.7% to 75.1%). Different techniques have been used to treat chronic neck pain. In this study, I will be comparing two manual therapy techniques along with stabilization exercises and will check which manual technique with stabilization exercise is more effective in the treatment of chronic neck pain. One of the techniques is Mulligan technique. The other one is the self-treatment approach of the McKenzie technique, . Additionally, cervical stabilization exercises, incorporating progressive stages, aim to enhance neuromuscular control.
The research involves two intervention groups (Group A and Group B) receiving specific treatments over 32 sessions within an eight-week period. Group A incorporates the Mulligan technique, cervical and scapulothoracic stabilization exercises, and transcutaneous electrical nerve stimulation (TENS) with a heating pad. Group B undergoes hot packs and TENS, followed by McKenzie exercises and cervical and scapulothoracic stabilization exercises. Outcomes, encompassing pain levels, range of motion (ROM), and Neck Disability Index (NDI) scores, will be evaluated using the Numeric Pain Rating Scale, Goniometer, and Neck Disability Scale. Data analysis will employ SPSS version 26. Data will be collected at baseline, immediately post-intervention, and at follow-up intervals.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Lahore, Punjab, Pakistan, 54000
- Riphah International University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 40-65 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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MCKENZIE AND STABILIZATION EXERCISES
In this group, 11 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 11 participants will receive McKenzie protocol with stabilization exercises.
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).
The exercises then repeated five or six times in a Session.
the session will be of 45 mins, 3 session per week.
At end of each session patients will do stabilization exercises with 10reps of each exercise with 10sec hold
Other Names:
|
|
Experimental: MULLIGAN AND STABILIZATION EXERCISES
In this group, 11 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 for 10 weeks
|
. The technique will include Self-sustained Natural Apophyseal Glide (SNAGs), Natural Apophyseal Glides (NAGs), and mobilization techniques..
The participants will receive three sets of Mulligan Mobilization, each set involving 10 repetitions of the exercise, with an interval of 15 to 20 seconds between the sets.At end of each session patients will do stabilization exercises with 10reps of each exercise with 10sec hold.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric pain rating scale
Time Frame: 4weeks
|
NPRS consists of a scale with 0-10 readings.
The zero denotes no pain while 1, 2, 3 denotes to mild pain, 4, 5, 6 denotes to moderate pain while 7-10 denotes to severe pain.
|
4weeks
|
|
Goniometer
Time Frame: 4 weeks
|
Active Range of Motion of the patient will be assessed using a universal standard goniometer for cervical flexion, extension, side flexion (left and right), rotation (left and right).
The data will be collected at baseline cervical goniometry.
|
4 weeks
|
|
Neck Disability Index (NDI)
Time Frame: 4 WEEKS
|
The NDI consists of ten questions.
Each question has six different assertions expressing progressive levels of pain or limitation in activities.
Item scores range from 0 (no pain or limitation) to 5 (as much pain as possible or maximal limitation).
The total NDI score ranges from 0 to 5 points.
Higher scores indicate greater disability.
|
4 WEEKS
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Sanaullah, ms, riphah lahore
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 NASHIA
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
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