Actively Recruiting

Phase Not Applicable
Age: 60Years - 75Years
All Genders
Healthy Volunteers
ID05296980

Validation of a Multidomain Neuropsychological Intervention for Individuals at Risk of Dementia: the REMINDER Program

Led by University of Coimbra · Updated on 2024-05-08

400

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

Sponsors

U

University of Coimbra

Lead Sponsor

F

Fundação para a Ciência e a Tecnologia

Collaborating Sponsor

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

Who Can Participate

Age: 60Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 60 or older
  • CAIDE dementia risk score greater than 8
  • 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
Not Eligible

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

AI-Screening

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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

Trial Site Locations

Total: 1 location

1

Faculty of Psychology and Educational Sciences

Coimbra, Portugal, 3002-115

Actively Recruiting

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Research Team

A

Ana Rita Silva, PhD

U

University of Coimbra

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...

https://pubmed.ncbi.nlm.nih.gov/41366742