Instrument-assisted Soft Tissue Mobilization and Kinesiotape Application in Individuals With Chronic Neck Pain.
- Conditions
- Cervical Pain
- Registration Number
- NCT04765670
- Lead Sponsor
- KTO Karatay University
- Brief Summary
Chronic neck pain causes errors in joint position sense. There are studies in the literature suggesting that instrument-assisted soft tissue mobilization and Kinesiotape applications improve the joint position sense. There is no study examining these applications acutely on joint position sense and pain in the cervical region. As a result of our study, we will compare the effects of single-session instrument-assisted soft tissue mobilization and Kinesiotape application on pain and joint position sense.
- Detailed Description
The study will be carried out on volunteers after the approval of the ethics committee. Before the research, individuals and / or their relatives will be informed about the purpose and content of the study. Volunteer individuals between the ages of 18-45 with chronic neck pain will be included in the study after obtaining their informed consent.
Participants will be randomly divided into two groups: Instrument assisted soft tissue mobilization and Kinesiotape Applications.
In the instrument-assisted soft tissue mobilization group, the trapezius and sternocleidomastoideus muscles will be applied in a single session for 90 seconds. Kinesiotape application will be applied to the trapezius and sternocleidomastoideus muscles in one session.
Pain will be evaluated with Visual Analog Scale and joint position sense will be evaluated with Cervical Range of Motion device before and after application.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Being diagnosed with chronic neck pain
- Being in the age range of 18-45
- Those with acute injury or infection,
- Those with open wounds,
- Osteoporosis,
- 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
- Identified as a history of surgery in the cervical region
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change from Baseline Cervical Pain at 2 minutes Baseline and 2 minutes after intervention Pain will be evaluated with Visual Analog Scale.
Change from Baseline Joint Position Sense at 2 minutes Baseline and 2 minutes after intervention Joint Position Sense will be evaluated Cervical Range of Motion Device
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
KTO Karatay University
🇹🇷Konya, Turkey
KTO Karatay University🇹🇷Konya, Turkey