IRCT20151122025191N3
Recruiting
Phase 3
Evaluation of Efficacy of multidomain interventions of diet, exercise, managing of vascular risk factors and cognitive training to prevent cognitive decline in Iranian older adults
Department of health and ageing - Department of population, family and school health0 sites196 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Major neurocognitive disorder.
- Sponsor
- Department of health and ageing - Department of population, family and school health
- Enrollment
- 196
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Aged 55 to 74 years.
- •Having at least one modifiable dementia risk factor from among hypertension, diabetes mellitus, dyslipidemia, obesity, abdominal obesity, abdominal obesity, metabolic syndrome, smoking, educational level less than 9 years, physical inactivity, and social inactivity.
- •No neurocognitive disorder detected by the psychiatrist with the use of DSM5 criteria at the base time.
- •The score 85 or more in the Addenbrooke cognitive test at the base time.
- •Able to independently perform the activities of daily living.
- •Can read and write in Farsi.
- •Able to participate in the exercise program safely.
- •Having a reliable informant who can provide investigators with requested information.
- •Providing written informed consent.
Exclusion Criteria
- •Existence of major psychiatric illness such as major depressive disorder.
- •Existence of other neurodegeneration disease such as Parkinson's disease.
- •The history of malignancy within the previous 5 years.
- •The history of cardiac stent or revascularization within the previous 1 year.
- •Existence of serious or unstable medical disease such as acute or sever asthma, active gastric ulcer, sever liver disease, or sever renal disease.
- •Existence of sever loss of vision or hearing, or communication disability.
- •Existence of any conditions preventing cooperation as judged by the study physician.
- •Existence of significant laboratory abnormality that may result in cognitive impairment.
- •The simultaneous participation in any other intervention trial.
Outcomes
Primary Outcomes
Not specified
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