- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04937985
Unsupported Upper Extremity Exercise Test in Chronic Neck Pain
Validity and Test-Retest Reliability of Unsupported Upper Limb Exercise Test in Patients With Chronic Neck Pain
The aim of this study was to examine the validity and test-retest reliability of unsupported upper extremity exercise test (UULEX) in individuals with chronic neck pain.
Patients with neck pain lasting at least 3 months will be included in the study. It is planned to examine the validity and test-retest reliability of the UULEX test in that patient groups.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Persons with chronic neck pain may limit the functional use of their upper extremities. It is recommended to determine appropriate upper extremity measurement methods in patients with chronic neck pain. Therefore the aim of this study was to examine the validity and test-retest reliability of unsupported upper extremity exercise test (UULEX) in individuals with chronic neck pain.
Six Minute Pegboard Ring Test, 30-Second Push-Up Test and Arm, Shoulder and Hand Injury Questionnaire (DASH), Visual Analog Scale, Neck Disability Index, New York Posture Rating Chart and Short Form-36 Health Survey were used to evaluate the validity of the test. For test-retest reliability, the unsupported upper extremity test was repeated 1 week later by the same investigator.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
İzmir, Turkey, 35620
- İlknur Naz Gürşan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 18-65 years old
Exclusion Criteria:
- Presence of additional disease affecting upper extremity and hand functions (carpal tunnel syndrome, trigger finger, impingement syndrome,thoracic outlet syndrome, lateral and medial epicondylitis, hand osteoarthritis, etc.),
- having undergone upper extremity or cervical region surgery
- cervical radiculopathy, rheumatic disease, presence of neurological symptoms
- According to the Visual Analogue Scale (VAS), neck pain intensity in activity is less than 3,
- Acute or chronic respiratory illness
- Cardiac disease
- Problem recognizing verbal commands
- Pregnancy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
UULEX Test Group
Patients with chronic neck pain
|
Performance tests consist of Six Minute Pegboard Ring Test, 30-Second Push-Up Test and Arm, Shoulder and Hand Injury Questionnaire (DASH), Neck Disability Index, New York Posture Rating Chart and Short Form-36 Health Survey.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional capacity test
Time Frame: 15 minutes- Change from baseline values at 1 week
|
Unsupported Upper Limb Exercise Test
|
15 minutes- Change from baseline values at 1 week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional capacity test
Time Frame: 6 minutes (single application)
|
Six minute pegboard ring test
|
6 minutes (single application)
|
|
Upper extremity endurance test
Time Frame: 30 seconds (single application)
|
30 Second Push Up Test
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30 seconds (single application)
|
|
Disability Level
Time Frame: 15 minutes (single application)
|
Neck Disability Index: Scores range from 0 to 50, with higher scores indicating higher disability
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15 minutes (single application)
|
|
Upper Extremity Function
Time Frame: 15 minutes (single application)
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Disability of Arm Shoulder and Hand Injury Questionnaire: Scores range from 0 to 100, with higher scores indicating higher disability
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15 minutes (single application)
|
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Severity of Pain
Time Frame: 3 minutes (single application)
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Visual analog Scale:Scores range from 0 to 100, with higher scores indicating higher pain severity
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3 minutes (single application)
|
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Postural Assessment
Time Frame: 10 minutes (single application)
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New York Posture Rating Chart :Scores range from 13 to 65, with higher scores indicating better posture
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10 minutes (single application)
|
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Quality of Life Assessment
Time Frame: 15 minutes
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Short Form-30 Health Survey: Scores range from 0 to 100, with higher scores indicating better quality of life
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15 minutes
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Zeynep Karazeybek, İzmir Katip Çelebi University
- Study Director: İlknur Naz, İzmir Katip Çelebi 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
- IKC3
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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