- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07241312
Relationship Between Muscle Oxygenation and Upper Extremity Exercise Capacity in Patients With Chronic Neck Pain
Investigation of the Relationship Between Muscle Oxygenation and Upper Extremity Exercise Capacity, Respiratory and Peripheral Muscle Strength, and Activities of Daily Living in Patients With Chronic Neck Pain
Study Overview
Status
Conditions
Detailed Description
Neck pain is an important public health problem that causes disability worldwide Chronic neck pain is defined as the presence of pain in an individual's neck area for more than twelve weeks. Chronic neck pain negatively affects the daily living activities of the individual; functional limitation causes job loss.
Neck pain has been observed to be associated with the trapezius muscle and impaired microcirculation in the trapezius muscle and inadequate muscle blood flow and oxygenation.
In addition, neck pain has been stated to reduce upper extremity performance. However, most of the results regarding the relationship between muscle activity and pain are not consistent. In addition, there are studies showing that respiratory muscles as well as peripheral muscles are affected in these patients. In the light of all this information, it was concluded that there may be a relationship between upper extremity exercise capacity and the oxygen level of the trapezius muscle and activities of daily living in patients with chronic neck pain. In this context, the aim of the study was to investigate the relationship between upper extremity exercise capacity and muscle oxygenation, muscle strength and activities of daily living in patients with chronic neck pain.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Kırşehir, Turkey (Türkiye)
- Kırşehir Ahi Evran University, Physical Therapy and Rehabilitation Center, Cardiopulmonary Unit
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with neck pain lasting at least 3 months due to one of the following problems: cervical strain or sprain, cervical disc lesions, cervical spondylosis, facet joint dysfunction, and myofascial pain syndrome.
Exclusion Criteria:
- Neck pain intensity during activity is below 3 points according to the Visual Analog Scale
- Upper extremity motor deficit on neurological examination
- Any surgery related to neck problems
- Cervical radiculopathy
- Any upper extremity surgery
- Any rheumatic and/or neurological disease or any disease affecting the vestibular system
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Chronic Neck Pain Group
Individuals between the ages of 18-65 who have had neck pain for at least 12 weeks, who were followed up in the Physical Therapy Outpatient Clinic of the Department of Physical Medicine and Rehabilitation will be included in the study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of Trapezius Muscle Oxygen Saturation
Time Frame: Day 1
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Patients' trapezius muscle oxygen saturation will be measured using a near infrared spectroscopy (Moxy® monitor (Moxy, Fortiori Design LLC, Minnesota, USA)).
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Day 1
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Evaluation of upper extremity capacity
Time Frame: Day 1
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Patients' upper extremity functional exercise capacity will be evaluated with six-minute pegboard and ring test.
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Day 1
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of peripheral muscle strength
Time Frame: Day 2
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Patients' shoulder abductor and shoulder flexor, elbow flexor and upper trapezius muscle strength will be evaluated with a portable hand dynamometer (KFORCE Muscle Controller®, KinventTM, France).
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Day 2
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Evaluation of respiratory muscle strength
Time Frame: Day 2
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An electronic mouth pressure device in accordance with American Thoracic Society and European Respiratory Society criteria will be used to evaluate respiratory muscle strength (Micro Medical MicroRM, UK).
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Day 2
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Evaluation of activity of daily living
Time Frame: Day 2
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The Glittre activity of daily living test will be used to evaluate patients' activities of daily living.
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Day 2
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Evaluation of upper extremity functional status
Time Frame: Day 1
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Upper Extremity Functional Index will be used to evaluate the upper extremity functional status of the patients.
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Day 1
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Başak KAVALCI KOL, PhD, Kirsehir Ahi Evran Universitesi
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
Other Study ID Numbers
- AhiEvranU530
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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