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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05826730
Other study ID # 2021 / 16
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 15, 2021
Est. completion date February 15, 2023

Study information

Verified date April 2023
Source Istinye University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Neck pain is one of the most frequently investigated and common musculoskeletal disorders that cause disability in the community.If neck pain is due to multifactorial etiology, it is defined as non-specific neck pain.Eccentric exercises are used to increase muscle strength and muscle mass. Non-specific neck pain affects negatively and often leads to severe disability. Various rehabilitation techniques are available to reduce pain and disability and increase functional level. This study aimed to compare the pain and functional status of eccentric exercise training and home program exercise groups of people with non-specific neck pain.


Description:

It is known that exercise treatments are useful in strengthening neck muscles and controlling postural disorders in patients with neck pain, which is currently accepted. Eccentric exercises are used to increase muscle strength and muscle mass. Home exercise and eccentric exercise training groups were included in a total of 24 sessions (8 weeks*3 days); home exercise program was applied to the individuals in the control group. Visual Analog Scale, Mc Gill Melzack Pain Assessment, Neck Disability Index, hand grip strength, and skin resistance assessments.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date February 15, 2023
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - diagnosed with Non-Specific neck pain by a physician - Having a complaint of non-specific neck pain for at least 3 months - Neck pain severity >40mm according to VAS - Voluntary participation of the individual in the study Exclusion Criteria: - Radiculopathy and structural defect in the cervical region, - Surgical history on the cervical region, - Inflammatory disease, - Severe psychological illness, - Presence of infection in bone and soft tissue in the cervical spine, - Malignancy, - Advanced osteoporosis, - Having upper extremity pathologies, - Having a neurological disease that will prevent treatment - Having previously undergone cervical region and spine surgery - To be included in the physiotherapy program from the neck and back region in the last 6 months, - In case of administration of drugs such as NSAIDs, opioids in the last 24 hours

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Eccentric Exercises
Eccentric Exercises for neck muscles.

Locations

Country Name City State
Turkey Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Istinye University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istinye University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Characteristics Pain frequency, duration before 8 weeks and end of the 8 weeks.
Primary Pain severity Visual analog scale-VAS before 8 weeks and end of the 8 weeks.
Primary Mcgill- Melzack Pain Questionnaire Mcgill- Melzack Pain Questionnaire before 8 weeks and end of the 8 weeks.the 24 session.
Secondary Disability Neck Disability index before 8 weeks and end of the 8 weeks.
Secondary Hand grip strength Digital Hand Dynamometer before 8 weeks and end of the 8 weeks.
Secondary Skin resistance Digital Multimeter before 8 weeks and end of the 8 weeks.
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