Testing the REMINDER Multidomain Neuropsychological Program
for Adults 60 to 75 at Risk of Dementia
Led by University of Coimbra · Updated on 2024-05-08
400
Participants Needed
1
Research Sites
126 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating a neuropsychological intervention called the REMINDER program designed to reduce the risk of dementia in older adults with increased risk. This study compares the REMINDER program to an active control group receiving psychoeducation about brain health and dementia risk factors. The trial aims to assess the effects of the program on cognitive function, daily functioning, neuropsychological measures, biomarkers, and dementia conversion rates over time.
The REMINDER program involves 20 therapist-led sessions lasting 45 to 60 minutes, delivered twice weekly over 12 weeks. It includes personal development activities, cognitive compensatory aids, goal setting, and behavior change techniques. The program is delivered either online via videoconferencing or face-to-face, with group and individual sessions to encourage social support and skill training. The control group participates in 20 psychoeducation sessions of the same length and frequency.
Participants will undergo assessments shortly after the intervention and at 6, 12, 18, and 24 months follow-up, including cognitive and functionality evaluations, blood biomarker tests, brain imaging, mood and quality of life measures, and self-efficacy questionnaires. Researchers will track adherence and measure the rate of progression from mild cognitive impairment to dementia. Total participation includes the 12-week intervention and extended follow-up for up to 24 months.
CONDITIONS
Brief Title
Validation of the REMINDER Dementia Risk Reduction Program
Research Team
A
Ana Rita Silva, PhD
U
University of Coimbra
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No significant cognitive impairment according to the Addenbrooke's Cognitive Examination-REVISED
No physical disabilities preventing study participation
Willing to complete all study activities for 12 weeks
You will not qualify if you...
Diagnosis of mild cognitive impairment or dementia
History of neurological events affecting cognition
Severe psychiatric disorders (mild depression or anxiety allowed)
Unable to travel to the session site (if applicable)
Illiteracy
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Outpatient Treatment
Duration - 12 weeks
Participants receive the REMINDER program or brain health psychoeducation sessions to promote cognitive reserve, socialization, and dementia risk reduction.
Twice weekly sessions totaling 20 sessions
Follow-up
Duration - Up to 24 months after the intervention
Participants are monitored for lasting effects on cognition, functionality, mood, and quality of life after the intervention.
Assessments at 1 week, 12 months, and 24 months post intervention
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
3
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Published Research Related To This Trial
REMINDER program: a randomized controlled trial protocol of a neuropsychological intervention for lifestyle modification in older adults at risk of dementia.
Ana Rita Silva, Catarina Baptista, Inês Baldeiras...