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The effect of phoenix Dactylifera supplementary on fatigue in patients with multiple sclerosis

Phase 3
Recruiting
Conditions
Multiple sclerosis.
Multiple sclerosis
Registration Number
IRCT20230706058689N1
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Having a history of MS for at least 3 months (based on the information in the patient's file)
Age 18 to 60 years
Absence of food and drug allergy (date products)
Obtaining a score of 28 or more in severe measurement (FSS)
Obtaining informed consent
Absence of pregnancy (pregnancy during the study period or decision to become pregnant at the beginning of the study)

Exclusion Criteria

The use of antidepressants
The use of other medications effective in relieving fatigue (Ritalin, Pemoline, Amantadine)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fatigue score based on the Fatigue Severity Scale (FSS). Timepoint: Measuring the severity of fatigue at the beginning (before the start of the intervention) and 6 weeks after the start of the intervention. Method of measurement: Fatigue severity scale Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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