- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06875856
Effects of Cailliet and Kendall Exercises in Nonspecific Neck Pain
Comparative Effects of Cailliet and Kendall Exercises on Pain, Functional Movement and Disability in Nonspecific Neck Pain: Randomized Control Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Pain felt in an area circumscribed superiorly by the superior nuchal line, laterally by the neck's lateral borders, and inferiorly by an imagined transverse line passing through the T1 spinous process is defined as neck pain. An acute or chronic cervical and shoulder girdle issue originating from the occiput of the head to the spine of the scapula, with or without limiting cervical range of motion, and unrelated to any past history of infection or fracture can be characterized as non-specific neck pain. One of the most common musculoskeletal issues that impairs general population function and results in disability is neck pain. The cervical spine is a complicated biomechanical system made up of at least 20 pairs of muscles, many of which have similar roles, and countless degrees of flexibility for each joint. However, the etiology and basic pathology of neck pain are still unknown. Around the world, 330 million people experience some form of neck pain with mean estimates of 7.6% prevalence (range, 5.9-38.7%), 37% annual prevalence (range, 16.7-75%), and 48.5% lifetime prevalence (range, 14.2-71%).
There have been contradictory findings from earlier studies about the optimal management of neck pain. While some contend that exercise leads to greater results, others support the efficacy of conventional therapy. Comparing the short-term benefits of the exercise programs designed by Cailliet and Kendall, in order to ascertain which method produces better results in terms of symptom relief and pain reduction. By getting empirical data on the short-term impacts of exercise treatments, the study will advance evidence-based practice. Healthcare practitioners can rely on this information to make well-informed decisions and recommendations because it will provide scientific proof on their safety and efficacy. This will support the use of a more standardized and empirically supported approach in the treatment of generalized neck pain symptoms associated with the neck musculature.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: imran amjad, PhD*
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Contact Backup
- Name: Imran Amjad, PHD*
- Phone Number: 0515481826
- Email: imran.amjad@riphah.edu.pk
Study Locations
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Punjab
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Lahore, Punjab, Pakistan, 54000
- Recruiting
- Good hands physiotherapy clinic
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Contact:
- Ghulam Fatima, PhD*
- Phone Number: 03034073057
- Email: ghulam.fatima@riphah.edu.pk
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Principal Investigator:
- Hafsa Mushtaq, MS*
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age group between 18 to 40 years
- Both gender male and female
- Individuals having localized pain or stiffness in spine or both combined between C3 and C7 without upper limb radiculopathy
- Negative Spurling's test, traction test, upper limb tension test, and shoulder abduction test.
- Pain reported on NPRS Moderate score in neck region for more than 3 months
- Neck Disability Index (NDI) score of 0-10 points out of 50 score
Exclusion Criteria:
- Tuberculosis, carcinoma, heart disease, and osteoporosis
- Neural disorders due to prolapsed intervertebral disc
- Any trauma, localized infection or history of surgery in cervical spine region in last 6 months
- Upper motor neuron disease, cervical stenosis, and metabolic diseases in bone and joint
- Hyper flexibility, Open sores
- Ongoing radiotherapy, chemotherapy, steroid therapy, or anticoagulants
- Psychiatric diseases such as phobia/obsession and depression
- Allergy to hot pack
Study Plan
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: Group A: Kendall exercises program
Group A will receive Kendall exercises program with baseline treatment.
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Active Comparator: Group B: Cailliet exercises program
Group B will receive Cailliet exercises program with baseline treatment.
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The intervention of group B will include baseline treatment, followed by maneuvers, including: Neck Cailliet exercise using isometric contractions against the prisoner to the maximum that ends with relaxation and continued with stretching.
Each posture was maintained for 30 s and 3 sets of 10 repetitions were performed with 3 sessions per week on alternate days for 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: 4 weeks
|
Pain intensity will be assessed by NPRS.
The NPRS has shown to have moderate to high test-retest reliability, ranging from 0.67 to 0.96.
The NPRS is shown to have convergent validity between 0.79 and 0.95.
The 11-point NPRS (intervals from 0-10) is used to quantify pain intensity; 0 represents no pain, and 10 represent the worst possible agony.
Zero indicates absence of pain while 5 indicate moderate pain and 10 indicate unbearable pain.
The patient is asked to mark a number on the scale.
At the baseline assessment, after 3 weeks and finally at the end of the intervention program, the NPRS scores will be recorded.
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4 weeks
|
|
Selective Functional Movement Assessment (SFMA)
Time Frame: 4 weeks
|
The Selective Functional Movement Assessment (SFMA) is a popular assessment tool used to observe and detect components of dysfunctional movement patterns.
The goal of the assessment is to identify impairments throughout the kinetic chain that may be contributing to movement dysfunction and/or pain.
Kappa coefficients for intra-rater reliability ranged from 0.21-1.00,
while % absolute agreement ranged from 0.64-1.00.
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4 weeks
|
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Neck Disability Index (NDI) for disability
Time Frame: 4 weeks
|
The neck disability index (NDI) is one of the most commonly used questionnaires to measure neck pain and disability.
One study reported that the NDI is a multidimensional construct that measures a broader concept than disability.
Each item is scored out of 5 for a maximum total score of 50.
Care should be taken in reporting the score as either out of 50 or as a percentage out of 100.
A score of 22% or more is considered a significant activities of daily living disability.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ghulam Fatima, PHD*, Riphah International University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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/24/0151
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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