Fibromyalgia Clinical Trial
Official title:
The Effect of Cherry Seed Pillow on Pain and Quality of Life in Patients With Fibromyalgia
Verified date | February 2024 |
Source | KTO Karatay University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this study, the effects of 4-week Cherry seed pillow application on pain and quality of life in individuals diagnosed with fibromyalgia will be examined.
Status | Completed |
Enrollment | 72 |
Est. completion date | February 10, 2024 |
Est. primary completion date | February 6, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - Over 18 years of age - Diagnosis of Fibromyalgia according to ACR classification criteria - Neuromuscular system examination is normal - Pain (vas-visual anologous scale) level of at least 5 points - No communication problems - Willingness to participate in the practice of using cherry seed cushion - To be capable of answering the data collection tools to be used in the research - Not having made hot, cold etc. applications at home Exclusion Criteria: - -No diagnosis of Fibromyalgia according to ACR classification criteria - Normal examination of the neuromuscular system - Pain (vas-visual anologous scale) level between 0-5 - Communication problems - Failure to accept the practice of using cherry seed cushion and failure to finish the implementation process - Having a musculoskeletal disorder other than fibromyalgia - Pregnant or lactating - To be capable of answering the data collection tools to be used in the research - Having made hot, cold etc. applications at home |
Country | Name | City | State |
---|---|---|---|
Turkey | KTO Karatay University | Konya | Karatay |
Lead Sponsor | Collaborator |
---|---|
Hasan Gerçek |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in pain at 4 weeks | he rest, activity and night pains of the participants will be evaluated with a 10 cm Visual Analog Scale before the treatment and at the end of the 4-week application. "0" means no pain, "10" means excruciating pain. Results will be recorded in cm. | Baseline and 4 weeks | |
Secondary | Change from baseline in function at 4 weeks | The Fibromyalgia Impact Questionnaire will be used to assess the functioning of the participants. The questionnaire consists of 20 questions. As the score increases, the function decreases. | Baseline and 4 weeks |
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