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effect of cognitive rehabilitation and life style modification on patients with mild cognitive intervention

Effectiveness of Cognitive Rehabilitation and Life Style Modification on Executive Function of Patients with Non Amnestic Mild Cognitive Impairment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203029188N1
Enrollment
45
Registered
2016-01-15
Start date
2014-09-20
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

mild cognitive impairment. Personal history of other mental and behavioural disorders

Interventions

Intervention 1: "Intervention group:" nine sessions of executive functions rehabilitation. Intervention 2: " Control group" will receive educational pamphlet of the other groups( after 6months)at the
Rehabilitation
Lifestyle
"Intervention group:" nine sessions of executive functions rehabilitation
" Control group" will receive educational pamphlet of the other groups( after 6months)at the end of the assessments.
" Intervention group": Nine sessions of life style educations in the same time with the other intervention group

Sponsors

Vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria :Age above 60 years; minimum 9 years of school education;NeuroCognitive Unite assesment (noucog) test score 75to 85 with executive function subscale score under 12 and memory subscale score above 15; /general Health Questioner(GHQ )test score under 22 ; physical ability to participate in training classes . Exclusion criteria : complaint of disability in daily activities, ; major psychiatric or neurological diagnosis ; diagnosis of dementia; substance abuse with effect on cognitive abilities ; use of psychotropic drug with effect on cognitive abilities

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Chenges of cognitive test's scores. Timepoint: Befor interventin-immediately after interventions-6months after intervention. Method of measurement: Go no go test.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6months after intervention. Method of measurement: Design fluency test.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6 months after intervention. Method of measurement: Five points test.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6 months after intervention. Method of measurement: Category fluency test.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6 months after intervention. Method of measurement: Tower of london test.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6 months after intervention. Method of measurement: BRIEF-A.;Chenges of cognitive test's scores. Timepoint: Before intervention-immediately after intervention-6 months after intervention. Method of measurement: Color trail making test.

Secondary

MeasureTime frame
Changes in scores of qialoty of life test. Timepoint: Before intervention-immediately after intervention-6months after intervention. Method of measurement: health promoting lifestyle test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Alavirad

Isfahan University of Medical Sciences

maryamalavirad@yahoo.com+98 31 3222 2135

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026