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Clinical Trials/ACTRN12608000489392
ACTRN12608000489392
Completed
未知

The Study of Mental Activity and Regular Training for the Prevention of Cognitive Decline in at Risk Individuals: The SMART Trial

niversity of Sydney0 sites100 target enrollmentSeptember 30, 2008

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Sydney
Enrollment
100
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 30, 2008
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 55 or above with a corrected Mini\-Mental State Exam score of 29 or below; willing to have multiple cognitive, physical and imaging assessments over 12 months; has a suitable informant (if available) that is willing and able to answer questions about their past and current condition; understands and agrees to comply with random allocation process; has telephone at home. There will be 3\-stage screening, which includes: Telephone screen by RA of participant and informant (if available) for willingness to participate, sedentary status, no exclusionary medical history, and TICS \< or equal to 30\. This will be followed by In\-person screen by neuropsychologist and later on by In\-person screen by geriatrician/stress testing (to ascertain unstable or unsuitable medical conditions).

Exclusion Criteria

  • Diagnosis of dementia, more than 1 stroke or transient ischemic attack (TIA) or major degenerative neurological disease; current psychotic illness diagnosis, current/past alcohol or drug abuse; current or past use of prescribed cognitive enhancing medication such as cholinesterase inhibitor, nootropic agents; no competency in English, or unable to read and write or use computers due to sensory impairment; high participation in mental activity; current participation in planned structured exercise of any kind other than low\- intensity walking 1 or more days per week; Activities of daily living (ADL) or instrumental activities of daily living (IADL) impairment due to cognition; non\-ambulatory; contraindications to high intensity progressive resistance training (PRT) or maximal exercise testing

Outcomes

Primary Outcomes

Not specified

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