MedPath

The Effect of Cherry Seed Pillow on Fibromyalgia

Not Applicable
Completed
Conditions
Fibromyalgia
Interventions
Other: Cherry seed pillow
Other: 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
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cherry seed pillowCherry seed pillow4 Weeks, 5 days a week, 20 minutes, in addition to the physiotherapy application of the routine, a heated cherry seed pillow will be applied.
ControlControl4 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
NameTimeMethod
Change from baseline in pain at 4 weeksBaseline 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
NameTimeMethod
Change from baseline in function at 4 weeksBaseline 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

© Copyright 2025. All Rights Reserved by MedPath