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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05785104
Other study ID # 012/004046
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date July 1, 2023

Study information

Verified date March 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to determine the effect of muscle energy technique versus myofascial release on cervical and lumbar pain in premenopausal women with fibromyalgia


Description:

Fibromyalgia is an idiopathic, non articular pain syndrome with generalized tender points. It is multisystem disease characterized by sleep disturbance and fatigue. It affect 5% of the world population. The incidence is higher in women than in men. And the age is between 30 and 35 years old.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date July 1, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 45 Years
Eligibility Inclusion Criteria: - Premenopausal women with fibromyalgia - Ages ranges between 30 - 45 years old - Body mass index < 35 kg/m2 - All are medically stable Exclusion Criteria: - specific cervical and lumbar pain - Smokers - Pregnant women - Medically unstable - Postmenopausal women

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Myofascial release
Is Facilitation of mechanical and neurological adaptive capacity as integrated through the Myofascial system
Muscle energy technique
Is manual therapy procedure that involves alternating periods of resisted muscle contraction and assisted stretching

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fibromyalgia impact questionnaire Used to assess health related quality of life before and after the treatment, maximum score means worse outcome Four weeks
Primary Visual analogue scale Used to assess the severity of cervical and lumbar pain of each premenopausal women in both groups before and after the treatment, maximum score means worse outcome Four weeks
Primary Active range of motion of cervical and lumbar regions Measurement of active flexion, extension, lateral flexion in cervical and lumbar regions before and after the treatment Four weeks
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