Unsupported Upper Extremity Exercise Test in Chronic Neck Pain

June 18, 2021 updated by: Ilknur Naz, Izmir Katip Celebi University

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

Completed

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

Observational

Enrollment (Actual)

44

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • İzmir, Turkey, 35620
        • İlknur Naz Gürşan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

44 patients with neck pain lasting at least 3 months and being volunteer to participate in our study

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

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
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
15 minutes (single application)
Upper Extremity Function
Time Frame: 15 minutes (single application)
Disability of Arm Shoulder and Hand Injury Questionnaire: Scores range from 0 to 100, with higher scores indicating higher disability
15 minutes (single application)
Severity of Pain
Time Frame: 3 minutes (single application)
Visual analog Scale:Scores range from 0 to 100, with higher scores indicating higher pain severity
3 minutes (single application)
Postural Assessment
Time Frame: 10 minutes (single application)
New York Posture Rating Chart :Scores range from 13 to 65, with higher scores indicating better posture
10 minutes (single application)
Quality of Life Assessment
Time Frame: 15 minutes
Short Form-30 Health Survey: Scores range from 0 to 100, with higher scores indicating better quality of life
15 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Zeynep Karazeybek, İzmir Katip Çelebi University
  • Study Director: İlknur Naz, İzmir Katip Çelebi University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2020

Primary Completion (Actual)

February 1, 2021

Study Completion (Actual)

February 1, 2021

Study Registration Dates

First Submitted

June 18, 2021

First Submitted That Met QC Criteria

June 18, 2021

First Posted (Actual)

June 24, 2021

Study Record Updates

Last Update Posted (Actual)

June 24, 2021

Last Update Submitted That Met QC Criteria

June 18, 2021

Last Verified

June 1, 2021

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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