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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04882397
Other study ID # KaratayUH3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 26, 2021
Est. completion date July 20, 2021

Study information

Verified date May 2021
Source KTO Karatay University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic neck pain causes errors in joint position. There are studies in the literature suggesting that the application of instrument-assisted soft tissue mobilization improves the sense of joint position. There are no studies that acutely examine this practice on joint position sense and pain in the cervical region. As a result of our study, we will investigate the effects of instrument-assisted soft tissue mobilization in a single session on perception of pain and joint position.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date July 20, 2021
Est. primary completion date June 26, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - • Being diagnosed with chronic neck pain, - To be in the age range of 18-65. Exclusion Criteria: - • Those taking any analgesic medication - Those with acute injury or infection, - Those with open wounds, Osteoporosis, - Broken, - Hematoma, Those with acute cardiac, liver and kidney problems, - Those with connective tissue disease, Rheumatoid arthritis, osteoarthritis, Cancer, - Those with circulation problems, - Those with peripheral vascular disease, Epilepsy, Surgery history in the cervical area

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Instrument Assisted Soft Tissue Mobilization
Bilateral Instrument assisted soft tissue mobilization application will be applied in a single session to the trapezius and sternocleideomastoideus muscles.
Sham
Bilateral sham Instrument assisted soft tissue mobilization application will be applied in a single session to the trapezius and sternocleideomastoideus muscles.

Locations

Country Name City State
Turkey KTO Karatay University Konya

Sponsors (1)

Lead Sponsor Collaborator
KTO Karatay University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline Cervical Pain at 2 minutes Pain will be evaluated with Visual Analog Scale. Baseline and 2 minutes after intervention
Primary Change from Baseline Joint Position Sense at 2 minutes Joint Position Sense will be evaluated Cervical Range of Motion Device Baseline and 2 minutes after intervention
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