Skip to content

Comparative Investigation efficacy of cognitive rehabilitation and donepezil on memory, attention, quality of life and depression in patients with multiple sclerosis.

Comparative Investigation efficacy of cognitive rehabilitation and donepezil on memory, attention, quality of life and depression in patients with multiple sclerosis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016042227522N1
Enrollment
80
Registered
2016-06-02
Start date
2016-05-30
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis. Demyelinating diseases of the central nervous system

Interventions

Intervention 1: Intervention group 1 : 20 hours Cognitive rehabilitation in 3 month period. Intervention 2: Intervention group 2 : Tab Donepezil 10mg daily for 3 month. Intervention 3: Intervention gr
Rehabilitation
Treatment - Drugs
Placebo
Intervention group 1 : 20 hours Cognitive rehabilitation in 3 month period
Intervention group 2 : Tab Donepezil 10mg daily for 3 month
Intervention group 3 :Tab Placebo daily for 3 month

Sponsors

Vice Chancellor Of Rsearch, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: definite diagnosis of MS according to the McDonald criteria by neurologist ; ability to participate in the interview and convey information and their experiences ; desire to participate in the study and necessary cooperation and motivation for interview ; absence of chronic disease other than multiple sclerosis ; age between 20 and 60 years ; having at least read and write education ; lack of renal and hepatic diseases ; non-use of anticholinergic drugs ; patients with Expanded Disability Status Scale up to 5/5 on the criteria of John Kurtzke ; patients with mild to moderate level of memory performance ; study of depression of subjects according to Beck for Primary Care questionnaire to verify the inclusion and omission of severe depression. Exclusion criteria: loss of each conditions during the study inclusion ; lack of desire to continue this research collaboration ; inability to participate in therapy sessions regularly ; relapses of disease during the intervention period that lead to hospitalization in the hospital.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Memory. Timepoint: Before Intervention & 3 month after Intervention. Method of measurement: Autobiographical Memory Test , The Prospective and Retrospective Memory Questionnaire , The Early Motor Questionnaire.;Attention. Timepoint: Before Intervention & 3 month after Intervention. Method of measurement: Digit Span Test.;Depression. Timepoint: Before Intervention & 3 month after Intervention. Method of measurement: Beck for Primary Care questionnaire.;Quality of Life. Timepoint: Before Intervention & 3 month after Intervention. Method of measurement: Quality of Life 54 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Mahdi Shahpouri

Isfahan University of Medical Sciences , Neurosciences Research Center

Shahpouri@resident.mui.ac.ir; Shahpouri2m@gmail.com; Mahdijan2010@yahoo.com+98 31 3780 7646

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 17, 2026