Making Memory Better for Seniors With Mild Cognitive Impairment
- Conditions
- Mild Cognitive Impairment
- Interventions
- Behavioral: Cognitive training
- Registration Number
- NCT01532739
- Lead Sponsor
- Nova Scotia Health Authority
- Brief Summary
The purpose of this study is to investigate the feasibility and effectiveness of a cognitive training group in individuals with Mild Cognitive Impairment, using a new paradigm that will optimize ecological validity by (1) focusing on everyday memory problems, (2) supplementing traditional memory training with the teaching of an empirically-supported problem-solving approach, and (3) employing a clinically representative sample of individuals with MCI (e.g., not excluding those with mild affective symptoms).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 40
- Clinical diagnosis of Mild Cognitive Impairment
- Clinical diagnosis of dementia
- History of neurological conditions known to impair cognition
- History of alcohol or drug abuse
- History of chronic psychiatric illness
- Current symptoms of moderate to severe depression (Geriatric Depression Scale >19) or anxiety (Beck Anxiety Inventory >15)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Cognitive training Cognitive training -
- Primary Outcome Measures
Name Time Method Change in everyday memory functioning Measured at baseline and months 3, 5, 8 Rivermead Behavioural Memory Test (3rd Edition)
- Secondary Outcome Measures
Name Time Method Change in memory perception Measured at baseline and months 3, 5, 8 Multifactorial Metamemory Questionnaire
Change on traditional memory testing Measured at baseline and months 3, 5, 8 California Verbal Learning Test (2nd Edition)
Change in quality of life Measured at baseline and months 3, 5, 8 Zarit Burden Interview
Change in mood (i.e., self-report symptoms of depression) Measured at baseline and months 3, 5, 8 Geriatric Depression Scale
Change in mood (i.e., self-report symptoms of anxiety) Measured at baseline and months 3, 5, 8 Beck Anxiety Inventory
Feasibility Measured at end of study Recruitment, retention, and compliance rates
Change in other psychiatric symptoms (informant-report) Measured at baseline and months 3, 5, 8 Neuropsychiatric Inventory
Change in caregiver burden Measured at baseline and months 3, 5, 8 Zarit Burden Interview
Trial Locations
- Locations (1)
Neuropsychology Service, Nova Scotia Hospital
🇨🇦Dartmouth, Nova Scotia, Canada