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
1 other identifier
interventional
32
1 country
1
Brief Summary
Objective of study will be to compare effects of Cailliet and Kendall exercises on pain, functional movement and disability in non-specific neck pain.This randomized clinical trial will be conducted at Good Hands Physiotherapy Clinic, Shahdara Lahore. Sample size of study will be 36. Participants will be randomly divided into two groups Group A and Group B. We will include patients with age group between 25 to 40 years, both genders having localized pain or stiffness in cervical spine for more than 3 months after exclusion of upper limb radiculopathy. Group A will receive Kendall exercises regime and Group B will receive Cailliet exercises regime. Both groups will receive baseline treatment including hot pack and Transcutaneous Electric Nerve Stimulation (TENS). Short term effects would be assessed after treatment for 3 sessions per week on alternate days for 4 weeks. Patients will be assessed by Numeric pain rating scale (NPRS) for pain, Selective Functional Movement Assessment (SFMA) for functional movement and Neck Disability Index (NDI) Urdu version for Disability. Analysis will be done by statistical package for social sciences SPSS 25.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 22, 2025
CompletedFirst Submitted
Initial submission to the registry
March 10, 2025
CompletedFirst Posted
Study publicly available on registry
March 13, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 3, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2025
CompletedMarch 13, 2025
March 1, 2025
7 months
March 10, 2025
March 12, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Numeric Pain Rating Scale
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.
4 weeks
Selective Functional Movement Assessment (SFMA)
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.
4 weeks
Neck Disability Index (NDI) for disability
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
Study Arms (2)
Group A: Kendall exercises program
EXPERIMENTALGroup A will receive Kendall exercises program with baseline treatment.
Group B: Cailliet exercises program
ACTIVE COMPARATORGroup B will receive Cailliet exercises program with baseline treatment.
Interventions
1. Positioning supine with the chin tucked in and lifting the head for 2 to 8 sec to strengthen deep cervical flexors. 2. Maintaining a sitting posture, with hands on the occipital region, and flexed spine while moving head downwards to stretch cervical extensors, maintaining an upright posture. 3. Keep the resistance band circling with strong support and stretching it with the upper limbs of both sides so that there is full retraction of the scapula to strengthen retractors of the shoulder. 4. Stretching the pectoralis major and minor while keeping the patient's hands-on the occipital region and standing behind the patient and pulling both elbows backward to target the bilateral pectoralis muscles
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Good hands physiotherapy clinic
Lahore, Punjab Province, 54000, Pakistan
Related Publications (1)
Bogduk N. The anatomy and pathophysiology of neck pain. Phys Med Rehabil Clin N Am. 2003 Aug;14(3):455-72, v. doi: 10.1016/s1047-9651(03)00041-x.
PMID: 12948338BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ghulam Fatima, PHD*
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 10, 2025
First Posted
March 13, 2025
Study Start
January 22, 2025
Primary Completion
September 3, 2025
Study Completion
September 15, 2025
Last Updated
March 13, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share