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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06922071
Acronym
REMINDER4Care
Enrollment
100
Registered
2025-04-10
Start date
2025-05-01
Completion date
2026-12-31
Last updated
2026-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Health, Dementia Risk Factors, Prevention

Keywords

Dementia Risk Factors, Prevention, Health, Aging, Residential and Daycare Facilities, Lifestyle

Brief summary

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.

Interventions

OTHERREMINDER4Care

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.

Sponsors

University of Coimbra
Lead SponsorOTHER
Fundação para a Ciência e a Tecnologia
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 65 years and older * RDF users * Elementary reading and writing skills

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
ScreeningScreeningParticipants' sociodemographic (e.g., age, marital status, education level) and clinical (presence of medical diagnosis, current medication, sensory issues, mobility deficits, substance use, and hospitalization).
Cognitive statusScreening and 1-week and 3-months post-interventionGlobal 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.
Mood statusScreening and 1-week and 3-months post-interventionDepressive 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.
Perceived social isolation and lonelinessBaseline and 1-week and 3-months post-interventionLoneliness: Measured with the UCLA Loneliness Scale (UCLA LS-3), the score was 20 to 80, with higher scores reflecting greater perceived loneliness.
Perceived social networkBaseline and 1-week and 3-months post-interventionSocial Networks: Evaluated using Lubben's Brief Social Network Scale (LSNS-6), scored from 0 to 30, where higher scores indicate a stronger social network.
Functionality statusBaseline and 1-week and 3-months post-interventionFunctional abilities: This is measured using the IAFAI (Informant Assessment of Functioning in Aging and Intellectual Disabilities).
Perceived quality of lifeBaseline and 1-week and 3-months post-interventionPsychological Well-Being: Assessed using the EBEP-R is a short version of the Psychological Well-Being Scale. Higher scores on the EBEP-R indicate better psychological well-being.

Countries

Portugal

Contacts

CONTACTCatarina L. B. Baptista, PhD Student
catarinalbbaptista23@gmail.com+351 963 031 318
PRINCIPAL_INVESTIGATORCatarina L. B. Baptista, PhD Student

University of Coimbra

STUDY_CHAIRAna Rita E. S. Silva, Doctorate

University of Coimbra

STUDY_CHAIRMargarida P. Lima, Doctorate

University of Coimbra

STUDY_CHAIRRosa M. Afonso, Doctorate

University of Beira Interior

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026