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The Effect of Cherry Seed Pillow on Fibromyalgia

The Effect of Cherry Seed Pillow on Pain and Quality of Life in Patients With Fibromyalgia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06171022
Enrollment
72
Registered
2023-12-14
Start date
2023-12-06
Completion date
2024-02-10
Last updated
2024-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibromyalgia

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.

Interventions

OTHERCherry seed pillow

4 Weeks, 5 days a week, in addition to the routine physiotherapy application, 20 minutes of heated cherry seed pillow will be applied to the participant's back area.

OTHERControl

4 Weeks, 5 days a week, in addition to the routine physiotherapy application, 20 minutes of hotpack will be applied to the participant's back area.

Sponsors

Hasan Gerçek
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in pain at 4 weeksBaseline and 4 weekshe 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

MeasureTime frameDescription
Change from baseline in function at 4 weeksBaseline and 4 weeksThe 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026