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Investigating effects of CO-OP approach on people with Multiple Sclerosis

Not Applicable
Recruiting
Conditions
Multiple Sclerosis.
Multiple sclerosis
Registration Number
IRCT20210621051643N1
Lead Sponsor
niversity of social welfare and rehabilitation sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Diagnosis of multiple sclerosis by a neurologist
Age between 18-50 years
EDSS score between 3 and 5.5
Score more than 26 in the MoCA assessment

Exclusion Criteria

Recurrence of symptoms or the onset of a new attack during the intervention period
History of receiving CO-OP treatment or similar treatments
Existence of neurological, rheumatic or orthopedic disorders that interfere with treatment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Participation and Satisfaction in Activity of Daily Living (ADL). Timepoint: Before the intervention ,After the intervention, follow-up period of 3 months. Method of measurement: Canadian Occupational Performance Measure (COPM).
Secondary Outcome Measures
NameTimeMethod
Depression score. Timepoint: Before intervention, after intervention, 3-month follow-up period. Method of measurement: Beck Depression Inventory II (BDI-II).;Quality of life score. Timepoint: Before intervention, after intervention, 3-month follow-up period. Method of measurement: Multiple Sclerosis Impact Scale (MSIS-29).;Social participation. Timepoint: Before intervention, after intervention, 3-month follow-up period. Method of measurement: Community Integration Questionnaire (CIQ).;Intensity and effect of fatigue. Timepoint: Before intervention, after intervention, 3-month follow-up period. Method of measurement: Fatigue Impact Scale (FIS) & Fatigue Severity Scale (FSS).
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