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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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04937985
Enrollment
44
Registered
2021-06-24
Start date
2020-11-01
Completion date
2021-02-01
Last updated
2021-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain, Upper Extremity Dysfunction

Keywords

chronic neck pain, upper extremity test, validity, reliability

Brief summary

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.

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.

Interventions

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.

Sponsors

Izmir Katip Celebi University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Functional capacity test15 minutes- Change from baseline values at 1 weekUnsupported Upper Limb Exercise Test

Secondary

MeasureTime frameDescription
Quality of Life Assessment15 minutesShort Form-30 Health Survey: Scores range from 0 to 100, with higher scores indicating better quality of life
Functional capacity test6 minutes (single application)Six minute pegboard ring test
Upper extremity endurance test30 seconds (single application)30 Second Push Up Test
Postural Assessment10 minutes (single application)New York Posture Rating Chart :Scores range from 13 to 65, with higher scores indicating better posture
Upper Extremity Function15 minutes (single application)Disability of Arm Shoulder and Hand Injury Questionnaire: Scores range from 0 to 100, with higher scores indicating higher disability
Severity of Pain3 minutes (single application)Visual analog Scale:Scores range from 0 to 100, with higher scores indicating higher pain severity
Disability Level15 minutes (single application)Neck Disability Index: Scores range from 0 to 50, with higher scores indicating higher disability

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026