The REMINDER4Care Program for Older Adults Supported by Residential and Daycare Facilities

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorUniversity of Coimbra

About this trial

Dementia incidence is rising, posing a public health challenge, but 45% of cases can be prevented by addressing modifiable risk factors. Multidomain trials show that lifestyle changes can improve cognitive function and reduce dementia risk (like the FINGER trial). The REMINDER program, a Portuguese-based dementia risk reduction protocol, was developed for community-dwelling older adults aged 55 and above. However, older adults in Residential and Daycare Facilities (RDF) have distinct needs that demand program adaptation to ensure its relevance and effectiveness. In addition, more studies are needed to evaluate the impact of multidomain interventions with older adults in RDF.

To address these challenges, the REMINDER4Care program was developed as a tailored, multidomain intervention to reduce dementia risk. It emphasizes social and cognitive engagement and advances its adaptation and evaluation in Residential and Daycare Facilities (RDF). To assess efficacy, the investigators will perform a Randomized Controlled Trial.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 65 years and older

RDF users

Elementary reading and writing skills

Disqualifiers

Have a clinical diagnosis of dementia and/or Mini-Mental State Examination (MMSE) scores below the cutoff for the presence of dementia (MMSE < 22-27, depending on education level)

Have a psychiatric or neurological condition that impairs cognition in the long term

Have sensory and functional deficits that compromise their participation in the neuropsychological assessment and throughout the intervention sessions

Trial design

Design model

Sequential

Treatments tested in this trial

  • REMINDER4Care

    Other intervention

    REMINDER4Care was an adapted version of the original REMINDER program, tailored to the characteristics, needs, and interests of older adults in RDF. The REMINDER4Care intervention includes 20 face-to-face group sessions, each approximately 60 to 75 minutes, held twice a week over ten weeks. This program aims to optimize memory, attention, executive function, and emotional regulation while promoting lifestyle habits that protect the aging brain. The sessions include brain health education, cognitive exercises, compensatory memory strategies, training for managing personally relevant goals (with goal setting), and stress management techniques (compassion-based therapies, relaxation methods, and mindfulness). Social support and emotion regulation strategies (like attention management, positive cognitive reappraisal, and reframing speech) were included to address psychosocial risk factors like stress, social isolation, and depression.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: REMINDER4Care interventionExperimental treatment 1 intervention
Group B: Waiting-list groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Screening

Participants' sociodemographic (e.g., age, marital status, education level) and clinical (presence of medical diagnosis, current medication, sensory issues, mobility deficits, substance use, and hospitalization).

Time frame
Screening
2

Screening

Dementia risk was assessed using the Lifestyle for BRAin health (LIBRA) score, which ranges from -2.1 to 10.6, with higher scores indicating a greater risk of developing dementia.

Time frame
Screening
3

Cognitive status

Global cognition was assessed using Addenbrooke's Cognitive Examination - Revised (ACE-R), a scale with scores ranging from 0 to 100, where higher scores indicate better cognitive functioning.

Time frame
Screening and 1-week and 3-months post-intervention
4

Mood status

Depressive Symptoms: Assessed using the Geriatric Depression Scale (GDS-30), a 30-item scale with scores ranging from 0 to 30, where higher scores indicate greater depressive symptoms.

Time frame
Screening and 1-week and 3-months post-intervention

Secondary outcomes

Other outcomes

Sponsors and contacts

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University of Coimbra

Lead sponsor

Fundação para a Ciência e a Tecnologia

Collaborator