Comparison of Three Different Exercise Training in Patients With Chronic Neck Pain: A Randomized Study

Biruni University1 site in 1 country45 target enrollmentAugust 8, 2022

ConditionsNeck Pain Pain, Neck

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Neck Pain
Sponsor: Biruni University
Enrollment: 45
Locations: 1
Primary Endpoint: Pain Intensity Assessment
Status: Completed
Last Updated: 3 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

Neck pain is a widespread problem in the general population and is second only to low back pain in musculoskeletal issues.

Detailed Description

The aim of this study is to compare the conventional therapy, cervical stabilization exercise approach, and core stabilization exercise in addiction to cervical stabilization in patients with chronic neck pain.

Registry

clinicaltrials.gov

Start Date

August 8, 2022

End Date

September 16, 2022

Last Updated

3 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Biruni University

Responsible Party

Principal Investigator

Eylül Pınar KISA

Clinical investigator

Biruni University

Eligibility Criteria

Inclusion Criteria

•Chronic neck pain more than 3 months
•Medically stable

Exclusion Criteria

•Patients with benign or tumors in the cervical region
•Patients with active, localized osseous and discal infection in the spine (spondylodiscitis)
•Patients with history of spinal fractures
•Patients with congenital anomaly
•Patients with neck surgery and spinal instability

Outcomes

Primary Outcomes

Pain Intensity Assessment

Time Frame: 4 weeks

The 11-point Verbal Numeric Pain Scale (VNPS; 0 means no pain; 10 means worst pain) will be use to assess pain intensity. The VNPS is a reliable and valid measure for subjective pain measurement. Participants will be asked to report the pain severity at that moment on a scale from 0 to 10.

Secondary Outcomes

Disability Evaluation(4 weeks)
Posture Evaluation(4 weeks)
Evaluation of Cervical Range of Motion(4 weeks)
Demografic Characteristic of Participants(1 week before the first treatment session)
Assessment of Quality of Life(4 weeks)