The Effect of Cherry Seed Pillow on Fibromyalgia
- Conditions
- Fibromyalgia
- Interventions
- Other: Cherry seed pillowOther: Control
- Registration Number
- NCT06171022
- Lead Sponsor
- Hasan Gerçek
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 72
- 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
- -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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cherry seed pillow Cherry seed pillow 4 Weeks, 5 days a week, 20 minutes, in addition to the physiotherapy application of the routine, a heated cherry seed pillow will be applied. Control Control 4 Weeks, 5 days a week, 20 minutes, in addition to the physiotherapy application of the routine, a hot-pack will be applied.
- Primary Outcome Measures
Name Time Method Change from baseline in pain at 4 weeks Baseline and 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.
- Secondary Outcome Measures
Name Time Method Change from baseline in function at 4 weeks Baseline and 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.
Trial Locations
- Locations (1)
KTO Karatay University
🇹🇷Konya, Karatay, Turkey