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Clinical Trials/NCT04100343
NCT04100343UnknownNot Applicable

Detection of Pattern of Unusual Signs and Symptoms of Multiple Sclerosis

Assiut University0 sites100 target enrollmentStarted: November 1, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Primary Endpoint
Fatigue severity scale

Study Overview

Brief Summary

Each Multiple Sclerosis patient will be submitted to Cognitive Abilities Screening Instrument (CASI), Expanded Disability Status Scale, Epowrth Sleeping Scale(ESS),Fatigue Severity Scale(FSS), Hamilton Depression Rating Scale, Hamilton Anxiety Rating Scale, Headache Disability Index, specific questionnaire based on International Headache Society (IHS) recommendations

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
30 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Male or female.
  • Age:30-50 years
  • Accepting all study requirement

Exclusion Criteria

  • comorbid patient e.g (diabetic, hypertensive.......etc )
  • opposition of the patient or their family

Outcomes

Primary Outcomes

Fatigue severity scale

Time Frame: 1 year

A self-report scale of nine items about fatigue, its severity and how it affects certain activities. Answers are scored on a seven point scale where 1 = strongly disagree and 7 = strongly agree. This means the minimum score possible is nine and the highest is 63. The higher the score, the more severe the fatigue is and the more it affects the person's activities. It is simple to understand and takes an average of eight minutes to answer

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mahmood Mohammed Yosry Abdelsatar Mohammed

Mahmood M. Yosry Abdelsatar

Assiut University

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