Trials Sponsors Conditions Drugs Pricing

Conditions

Neck Pain

Outcome Measures

Primary Outcomes (6)

Upper extremity functional exercise capasity
Upper extremity exercise capacity will be evaluated with the six-minute pegboard and ring test (6-PBRT). In the test, as the number of rings increases, exercise capacity also increases.
Baseline
Pain severity
Pain intensity will be assessed with the Visual Analog Scale. It is scored between 0-10 and the higher the score, the greater the pain intensity.
Baseline
Pain threshold
Pain threshold will be assessed with an algometer. An increase in the applied pressure indicates a higher pain threshold.
Baseline
Functional levels
Functional status related to the upper extremity will be assessed using the QuickDASH. QuickDASH scores range from 0 to 100, where 0 indicates no disability and 100 indicates the most severe disability.
Baseline
Muscle strength
Shoulder abductors and hand grip strength will be assessed using a hand dynamometer.
Baseline
Life quality
The SF-36 will be used to measure changes in quality of life levels associated with chronic neck pain. Scores on the scale range from a minimum of 0 to a maximum of 100; higher scores indicate a better quality of life.
Baseline

Study Arms (2)

Chronic neck pain

Individuals with chronic non-specific neck pain will be included in the study.

Control Group

Healthy and voluntary participants will be included in the study.

Eligibility Criteria

Age18 Years - 65 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Patients with chronic neck pain and healthy individuals

You may qualify if:

For the patient group:

Sponsors & Collaborators

Karabuk University
Otherlead

Study Sites (1)

Karabuk University, Physiotherapy and Rehabilitation Application and Research Center

Karabük, Turkey (Türkiye)

RECRUITING

Musa Güneş, MsCCONTACT+905315132482 musagunes@karabuk.edu.tr

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

Musa Güneş, PhD
Karabuk University
STUDY CHAIR

Central Study Contacts

Musa Güneş, PhD

CONTACT

03704789081 musagunes@karabuk.edu.tr

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: CROSS SECTIONAL
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Principal Investigator, PhD

Study Record Dates

First Submitted

October 20, 2026

First Posted

October 28, 2026

Study Start

May 30, 2026

Actual (reported)

Primary Completion

December 20, 2026

Estimated

Upper Extremity Exercise Capacity in Chronic Non-specific Neck Pain

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (6)

Study Arms (2)

Chronic neck pain

Control Group

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (6)

Study Arms (2)

Chronic neck pain

Control Group

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations