- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06233006
Investigation of the Effects of Upper Extremity Functions in Female Patients With Non-Specific Neck Pain
Investigation of the Effects of Upper Extremity Functions and Health-Related Quality of Life in Female Patients With Non-Specific Neck Pain
Non-specific neck pain is defined as pain in the posterior and lateral part of the neck between the superior nuchael line and the spinous process of the 1st thoracic vertebra, without neurological findings and obvious structural pathology. It is more common in women than in men. Neck pain is thought to affect upper extremity functions. Although the exact cause is unknown, it has been reported that mechanical loading, minor peripheral nerve damage and deconditioning negatively affect upper extremity functions in individuals with neck pain and reduce the quality of life. Although it is stated in the literature that patients with neck pain often experience upper extremity problems, there are a limited number of studies evaluating the relationship between the neck and upper extremity.
This study was planned to determine upper extremity functions and their impact on health-related quality of life in female patients with NSHP. Female patients with NSHP over the age of 18 who apply to Tarsus State Hospital Physical Therapy and Rehabilitation Clinic, meet the inclusion criteria, and agree to participate in the study will be included in the study. With our research, patients' upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life will be evaluated and interpreted.
Study Overview
Detailed Description
Non-specific neck pain is defined as pain in the posterior and lateral part of the neck between the superior nuchael line and the spinous process of the 1st thoracic vertebra, without neurological findings and obvious structural pathology. It is more common in women than in men. Neck pain is thought to affect upper extremity functions. Although the exact cause is unknown, it has been reported that mechanical loading, minor peripheral nerve damage and deconditioning negatively affect upper extremity functions in individuals with neck pain and reduce the quality of life. Although it is stated in the literature that patients with neck pain often experience upper extremity problems, there are a limited number of studies evaluating the relationship between the neck and upper extremity.
This study was planned to determine upper extremity functions and their impact on health-related quality of life in female patients with NSHP. Female patients with NSHP over the age of 18 who apply to Tarsus State Hospital Physical Therapy and Rehabilitation Clinic, meet the inclusion criteria, and agree to participate in the study will be included in the study. With our research, patients' upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life will be evaluated and interpreted.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Abdulkadir Goz
- Phone Number: +905064042401
- Email: fzt.kadir@hotmail.com
Study Locations
-
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Tarsus
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Mersin, Tarsus, Turkey, 33400
- Recruiting
- Tarsus State Hospital
-
Contact:
- Abdulkadir Goz, MsC
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Having neck pain lasting more than 30 days and being diagnosed with non-specific neck pain
- Having a score of 14/50 or above on the Neck Disability Index
- Expressing neck pain as at least 3/10 points or above on the visual analog scale
- Being 18 years or older
- Female patients
Exclusion Criteria:
- Previously diagnosed orthopedic diseases related to the spine
- Undergoing surgical upper extremity surgery that may affect upper extremity functions
- Being pregnant and having just given birth
- Serious pathologies (such as cancer, spondylolisthesis, rheumatoid arthritis, kyphoscoliosis, scoliosis, etc., thoracic deformity or ankylosing spondylitis)
- Symptoms of cervical spinal stenosis (such as incoordination of hands, arms and legs, bowel and bladder incontinence)
- Radix compression (such as sensory changes, muscle weakness, or decreased reflexes)
- History of whiplash or cervical surgery
- Kyphoscoliosis, scoliosis etc. thorax deformity
- Having a body mass index over 30
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Non Spesific Neck Pain
Patients with Non Spesific Neck Pain
|
upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life
|
Healthy Control
Individuals with similar age
|
upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
hand skills
Time Frame: 4 minutes
|
Assessed with Nine Hole Peg Test
|
4 minutes
|
hand grip strength
Time Frame: 1 minute
|
Assessed with Baseline Hand Dynamometer
|
1 minute
|
pinch grip strength
Time Frame: 1 minute
|
Assessed with Baseline Pinchmeter
|
1 minute
|
reaction time
Time Frame: 1 minute
|
Assessed with Nelson Hand Reaction Test
|
1 minute
|
position sense
Time Frame: 5 minutes
|
Assessed with Baseline Digital Inclinometer
|
5 minutes
|
Upper extremity strength and endurance
Time Frame: 1 minutes
|
Assessed with Single Arm Military Press Test
|
1 minutes
|
upper extremity disability
Time Frame: 5 minutes
|
Assessed with DASH questionnarie
|
5 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Health Related Quality of Life
Time Frame: 5 minutes
|
Assessed with SF36 quastionnarie
|
5 minutes
|
Neck disability
Time Frame: 5 minutes
|
Assessed with Neck Disability Index
|
5 minutes
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Sevgi OZALEVLİ, PhD, Dokuz Eylül University
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 (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DokuzEU01
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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