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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06171022
Other study ID # KaratatUH10
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 6, 2023
Est. completion date February 10, 2024

Study information

Verified date February 2024
Source KTO Karatay University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cherry 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.
Control
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.

Locations

Country Name City State
Turkey KTO Karatay University Konya Karatay

Sponsors (1)

Lead Sponsor Collaborator
Hasan Gerçek

Country where clinical trial is conducted

Turkey, 

Outcome

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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