- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06927609
Kendall Exercises on Posture-Related Cervical Spondylosis
Effects of Kendall Exercises on Posture-Related Cervical Spondylosis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study investigates the impact of Kendall exercises on posture-related cervical spondylosis, a degenerative condition often linked to postural deviations like forward head posture (FHP). Prolonged poor posture, frequently exacerbated by activities such as excessive smartphone or computer use, leads to muscle imbalances, increased mechanical stress on the cervical spine, and degenerative changes in intervertebral discs and joints.
Kendall exercises are targeted therapeutic interventions designed to address muscle imbalances by strengthening weak muscles (e.g., deep cervical flexors) and stretching tight muscles (e.g., upper trapezius, pectoralis muscles). These exercises aim to restore proper alignment, reduce mechanical strain, and improve overall posture and cervical function.
Participants with posture-related cervical spondylosis will engage in a four-week exercise protocol involving specific Kendall exercises for cervical extensors, flexors, shoulder retraction, and chest muscles. Outcomes will be assessed using craniovertebral angle measurements, photographic analysis, and subjective pain/function scales. The study seeks to establish Kendall exercises as a non-invasive, effective intervention for managing cervical spondylosis by correcting postural deviations and mitigating associated symptoms
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
KPK
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Malakand, KPK, Pakistan
- DHQ Hospital, Batkhela, and Bahadur Khan, Rozi Khan Memorial Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Already diagnosed patients of cervical radiculopathy confirmed by clinical examination and imaging
- A patient with a Forward Head Posture (FHP) (CVA angle less the 48-50 degrees is defined as Forward head posture
- Positive Spurling test
- Numbness of the arm, fingers, or shoulder
- Cervical Postural assessment showing asymmetry (radiographic Analysis, and Posture Observation)
- Chronic symptoms ≥ 1 year
- Pain and Stiffness which limited range of motion in the cervical spine (Flexion less than 60°) (Extension less than 73°) (Lateral Flexion less than 13°-23° Rotation less than 80°)
- Pain: moderate to severe level (≥5 on NPRS)
Exclusion Criteria:
• History of Recent trauma to the cervical spine
- Any psychological condition
- Any specific cause of cervical radiculopathy (e.g., metabolic diseases, rheumatoid arthritis, osteoporosis)
- Central or peripheral neurological signs
- History of spinal surgery.
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: (Kendall Exercises)
Stretching of Cervical Extensors Strengthening Deep Cervical Flexors Strengthening Shoulder Retraction Stretching Pectoralis Muscle
|
Stretching of Cervical Extensors Strengthening Deep Cervical Flexors Strengthening Shoulder Retraction Stretching Pectoralis Muscle
|
|
Active Comparator: conventional therapy
Cervical Traction Neck Isometric Exercises (Cervical flexors), Static Stretching (Cervical extensors) General Cervical Extension and Flexion Exercises Shoulder Shrugs
|
Cervical Traction Neck Isometric Exercises (Cervical flexors), Static Stretching (Cervical extensors) General Cervical Extension and Flexion Exercises Shoulder Shrugs
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Range Of Motion: Goniometer
Time Frame: 4 weeks
|
A goniometer is a tool used to measure joint angles and range of motion (ROM).
The goniometer has high intra-rater and inter-rater reliability when used by trained professionals.
Consistent measurement can be achieved with proper technique and positioning.
It provides valid measurements of joint ROM when compared with other objective measures such as radiographic assessments.
|
4 weeks
|
|
craniovertebral angle (CVA)
Time Frame: 4 weeks
|
The Craniovertebral Angle is one of the most reliable methods and common angles for evaluating the Forward head posture.
It is the angle between a line drawn from the tragus of the ear to the C7 vertebra and a line drawn horizontally.
A reduced CVA indicates a forward head posture.
|
4 weeks
|
|
Neck Disability Index (NDI)
Time Frame: 4 weeks
|
The Neck Disability Index (NDI) is a widely used self-reported questionnaire that measures the patient's perceived disability due to neck pain.
It consists of 10 items, each scoring from 0 to 5, covering various aspects such as pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation.
Cronbach's alpha value for NDI was found to be .95
and this was statistically significant (p<.01).
|
4 weeks
|
|
Numeric Pain Rating Scale (NPRS)
Time Frame: 4 weeks
|
The Numeric Pain Rating Scale is an eleven-point pain impression scale: the patient rates pain from 0 (no aggravation) to 10 (most exceedingly terrible possible pain).
Mild 1-3, Moderate 4-6, Severe 7-10.
It has good test-retest reliability (r=.79-.96) in individuals with chronic pain and musculoskeletal pathology.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria khalid, MSOMPT, Riphah International University
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/muhammad talha 02008
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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