- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05826730
Eccentric Exercise in Patients With Non-Specific Neck Pain
Investigation of The Effect of Eccentric Muscle Training on Pain and Functionality in People With Non-Specific Neck Pain
Neck pain is one of the most frequently investigated and common musculoskeletal disorders that cause disability in the community.If neck pain is due to multifactorial etiology, it is defined as non-specific neck pain.Eccentric exercises are used to increase muscle strength and muscle mass.
Non-specific neck pain affects negatively and often leads to severe disability. Various rehabilitation techniques are available to reduce pain and disability and increase functional level.
This study aimed to compare the pain and functional status of eccentric exercise training and home program exercise groups of people with non-specific neck pain.
Study Overview
Detailed Description
It is known that exercise treatments are useful in strengthening neck muscles and controlling postural disorders in patients with neck pain, which is currently accepted. Eccentric exercises are used to increase muscle strength and muscle mass.
Home exercise and eccentric exercise training groups were included in a total of 24 sessions (8 weeks*3 days); home exercise program was applied to the individuals in the control group. Visual Analog Scale, Mc Gill Melzack Pain Assessment, Neck Disability Index, hand grip strength, and skin resistance assessments.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Istanbul, Turkey, 34010
- Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Istinye University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- diagnosed with Non-Specific neck pain by a physician
- Having a complaint of non-specific neck pain for at least 3 months
- Neck pain severity >40mm according to VAS
- Voluntary participation of the individual in the study
Exclusion Criteria:
- Radiculopathy and structural defect in the cervical region,
- Surgical history on the cervical region,
- Inflammatory disease,
- Severe psychological illness,
- Presence of infection in bone and soft tissue in the cervical spine,
- Malignancy,
- Advanced osteoporosis,
- Having upper extremity pathologies,
- Having a neurological disease that will prevent treatment
- Having previously undergone cervical region and spine surgery
- To be included in the physiotherapy program from the neck and back region in the last 6 months,
- In case of administration of drugs such as NSAIDs, opioids in the last 24 hours
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 |
---|---|
Active Comparator: Exercise
Eccentric muscle training for neck muscles
|
Eccentric Exercises for neck muscles.
|
No Intervention: Control
Home exercise program for neck muscles
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Characteristics
Time Frame: before 8 weeks and end of the 8 weeks.
|
Pain frequency, duration
|
before 8 weeks and end of the 8 weeks.
|
Pain severity
Time Frame: before 8 weeks and end of the 8 weeks.
|
Visual analog scale-VAS
|
before 8 weeks and end of the 8 weeks.
|
Mcgill- Melzack Pain Questionnaire
Time Frame: before 8 weeks and end of the 8 weeks.the 24 session.
|
Mcgill- Melzack Pain Questionnaire
|
before 8 weeks and end of the 8 weeks.the 24 session.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disability
Time Frame: before 8 weeks and end of the 8 weeks.
|
Neck Disability index
|
before 8 weeks and end of the 8 weeks.
|
Hand grip strength
Time Frame: before 8 weeks and end of the 8 weeks.
|
Digital Hand Dynamometer
|
before 8 weeks and end of the 8 weeks.
|
Skin resistance
Time Frame: before 8 weeks and end of the 8 weeks.
|
Digital Multimeter
|
before 8 weeks and end of the 8 weeks.
|
Collaborators and Investigators
Sponsor
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
- 2021 / 16
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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