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The Effect of Acupressure on Severity of Fatigue and Pain of Multiple Sclerosis (MS) disease in female members of MS Association.

Not Applicable
Conditions
multiple sclerosis.
multiple sclerosis
Registration Number
IRCT201108276247N2
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

women with stable vital signs; lack of wounds and deformity in the LI4( When the thumb is in full extension, the middle point of the angle between the first and second metacarpal), ST36(The width of a finger tip to the side with the lower edge of the tibia 3 cun below the knee), SP6(or sanyingiao 3 cun above the inner ankle to the back edge of the posterior tibia); being able to read and write; confirmed fatigue related to MS; no history of using acupressure; no history of smoking, using drugs or pills; age between18-40 and EDSS is between 0-5.5.
Exclusion criteria: unwillingness to continue participation in the trial; complications during the procedure; known physical and mental disorders; being perform the acupressure point 4LI, ST36, SP6 and don't have any sense of warmth, heaviness, swelling or numbness and not performing more than a quarter of days.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain reduction. Timepoint: Before the intervention, immediately after, two weeks after the first two weeks after the last intervention. Method of measurement: Visual analog scale.;Fatigue reduction. Timepoint: Before the intervention, immediately after, two weeks after the first two weeks after the last intervention. Method of measurement: Fatigue Severity Scale.
Secondary Outcome Measures
NameTimeMethod
Severity of pain. Timepoint: Before the intervention, immediately after, two weeks after the intervention and four weeks after the first intervention. Method of measurement: Visual analog scale.;Severity of fatigue. Timepoint: Before the intervention, immediately after, two weeks after the intervention and four weeks after the first intervention. Method of measurement: Fatigue Severity Scale.
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