Skip to content

REACT MCI - Repeated Advanced Cognitive Training in Mild Cognitive Impairment

Repeated Advanced Cognitive Training in Mild Cognitive Impairment (The REACT MCI Study). A Randomized, Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04792528
Acronym
REACT MCI
Enrollment
205
Registered
2021-03-11
Start date
2021-05-15
Completion date
2028-10-25
Last updated
2026-04-30

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

Conditions

Mild Cognitive Impairment

Keywords

computer-based cognitive training

Brief summary

Background: Dementia is a debilitating and devastating disease impacting the individuals, their families, and the health care system. According to the World Health Organization the dementia epidemic could overwhelm the global health care system and undermine social and economic development. Currently, no curative treatment for dementia exists despite immense research activity. The cognitive and functional impairment in dementia, especially Alzheimer's disease (AD), develop slowly decades before clinical signs emerge. This knowledge has led to the recognition of a prodromal period of mild cognitive impairment (MCI), between normal cognition and dementia. This is at present the earliest stage for intervention in dementia; even a short delay in dementia progression will have a large impact on global economy and health care. Objectives: In this clinical multicenter study, we aim to investigate the efficiency and cost-effectiveness of working memory training in MCI. To identify high responders to training analysis of genetic markers, relative's stress and craniospinal clearance will be performed. Participants and methods: This study is a blinded, randomized and controlled trail that will include 213 participants, diagnosed with MCI, included from five Norwegian Memory clinics in four health care regions. The groups will be randomized to either two training periods, one training period or active control. The intervention is computerized working memory training. Neuropsychological status, activities of daily living (ADL), and relative stress and quality of life will be assessed at baseline and 3, 6, 12 ,24 and 48 months after training. Structural MRI will be performed at baseline, and 3 and 6 months after training. For participants in the REACT MCI glymphatics substudy craniospinal clearance will be measured at baseline. A cost-utility analysis will be performed to evaluate if the working memory training is more cost-effective compared to the active control group in the MCI phase, taking a societal perspective.

Interventions

OTHERComputerized cognitive training.

COGMED RM program (Pearson Inc., UK)

OTHERGeneralized brain training / Active control

Solitaire

Sponsors

Sorlandet Hospital HF
Lead SponsorOTHER_GOV
Oslo University Hospital
CollaboratorOTHER
NKS Olaviken
CollaboratorUNKNOWN
St. Olavs Hospital
CollaboratorOTHER
NKS Kloverasen
CollaboratorUNKNOWN
Barrow Neurological Institute
CollaboratorOTHER
University of Maryland
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

All study personnel except for the PI, coaches and Study secretary will be blinded for group allocation regarding types of memory training.

Intervention model description

Randomization in blocks of six to eight will be performed by the regional research support statistics service to either two training periods, one training period or generalized brain training/active control.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

for the REACT MCI study: * Diagnosis of MCI, based on the Mayo/winblad criteria or confirmation of current MCI status within the last 6 months before study enrollment. * The ability to use and accessibility to an iPad or computer. * Fluent in Norwegian. * Spinal tap performed and results available

Exclusion criteria

for the REACT MCI study: * Patients unable to undergo a MRI investigation based on claustrophobia or metal foreign bodies are excluded from the study. * Major psychiatric illness and current substance abuse * Recent stroke Inclusion Criteria for the REACT MCI Glymphatics substudy: * Enrollment in the REACT MCI study * Participant allocated to Sorlandet Hospital or Oslo University Hospital

Design outcomes

Primary

MeasureTime frameDescription
Working memory training is superior to active control measured by spatial span backwards at 6 monthsFrom enrollment until 6 months
Reduced function in the glymphatic system is associated with reduced working memory training effect measured by CT evaluated craniospinal clearanceEnrollment to 12 monthsCraniospinal clearance will be evaluated with a single CT image scan at level with the foramen magnum.
Working memory training impact quality of life measure in the participants as compared to active control measured by EuroQOL5D-5L after 12 months.Enrollment to12 months
Working memory training prolongs the MCI phase as compared to active controlsEnrollment to 48 monthsWe consider the participants as having dementia when they no longer rapport intact activities of daily living and in addition display reduction of 1.5 standard deviation on test score on two tests on three or more cognitive domains.

Secondary

MeasureTime frameDescription
The effect of working memory training is dose related measured by spatial span backwards after 6 monthsEnrollment to 6 months
Allelic variations in predefined genetic markes influence training effects after 3 months measured by spatial span backwards.Enrollment to 3 monthsAllelic variations of LMX1a, APOE, AQP4 and/or COMT have in previous publications shown variable impact on working memory training. A statistical model combining these genes will be fitted for this investigation
Workin memory training reduces relatives stress scores as compared to relatives stress scores in the active control group after 12 monthsEnrollment to 12 monthsRelatives stress score (RSS) is a validated scale measuring the stress for relatives
Working memory training reduces QALY associated cost as compared to active controls at 24 months.Enrollment to 24 monthsThe generic outcome in the analysis is QALYs (Quality adjusted life years) derived from the instrument EQ-5D 5L. The second outcome is production loss of the relatives and patients associated with MCI through the progression of dementia The health economic analysis will include following costs: 1) intervention related costs 2) direct costs/health care costs, mainly related to use of health care services, including primary, secondary and tertiary care and health services 3) indirect costs, including work absence for the patients and the relatives of the patients (i.e., productivity loss). Data will be collected through a self-report measures (EQ-5D 5L), and from the Norwegian patient registry.
Working memory training reduces QALY associated cost as compared to active controls at 48 months.enrollment to 48 monthsThe generic outcome in the analysis is QALYs (Quality adjusted life years) derived from the instrument EQ-5D 5L. The second outcome is production loss of the relatives and patients associated with MCI through the progression of dementia The health economic analysis will include following costs: 1) intervention related costs 2) direct costs/health care costs, mainly related to use of health care services, including primary, secondary and tertiary care and health services 3) indirect costs, including work absence for the patients and the relatives of the patients (i.e., productivity loss). Data will be collected through a self-report measures (EQ-5D 5L), and from the Norwegian patient registry.

Countries

Norway

Contacts

PRINCIPAL_INVESTIGATORSusanne S Hernes, M.D. Phd.

Sørlandet Sykehus HF, Universitetet i Bergen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026