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REACT MCI - Repeated Advanced Cognitive Training in Mild Cognitive Impairment (REACT MCI)

Primary Purpose

Mild Cognitive Impairment

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Computerized cognitive training.
Generalized brain training / Active control
Sponsored by
Sorlandet Hospital HF
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild Cognitive Impairment focused on measuring computer-based cognitive training

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Exclusion Criteria for the REACT MCI Glymphatics substudy:

  • Individuals with known allergy against contrast solutions
  • Individuals with other serious allergies
  • Individuals with kidney failure or glomerular filtration rate < 30
  • Individuals younger than 18 or older than 80
  • Pregnant or lactating women
  • For individuals >70 years or with medications affecting kidney function the glomerular filtration rate needs to be less than week old.

Sites / Locations

  • Sørlandet Sykehus ArendalRecruiting
  • NKS Olaviken Alderspsykiatriske sykehus - HukommelsesklinikkRecruiting
  • N.K.S. KløveråsenRecruiting
  • Oslo Universitetssykehus UllevålRecruiting
  • St. Olavs HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

One training period

Two training periods

Active control

Arm Description

One training period of 30 minutes of daily adaptive training for 4-5 days a week up for 20- 25 trainings using computerized cognitive training.

Two training periods of 30 minutes of daily adaptive training for 4-5 days a week up for 20- 25 trainings using computerized cognitive training.

The generalized brain training group (Active control) will play solitaire 30 minutes daily for 25 sessions

Outcomes

Primary Outcome Measures

Working memory training is superior to active control measured by spatial span backwards at 6 months
Reduced function in the glymphatic system is associated with reduced working memory training effect measured by CT evaluated craniospinal clearance
Craniospinal 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.
Working memory training prolongs the MCI phase as compared to active controls
We 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 Outcome Measures

The effect of working memory training is dose related measured by spatial span backwards after 6 months
Allelic variations in predefined genetic markes influence training effects after 3 months measured by spatial span backwards.
Allelic 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 months
Relatives 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.
The 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.
The 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.

Full Information

First Posted
February 23, 2021
Last Updated
February 3, 2023
Sponsor
Sorlandet Hospital HF
Collaborators
Oslo University Hospital, NKS Olaviken, St. Olavs Hospital, NKS Kloverasen, Barrow Neurological Institute, University of Maryland
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1. Study Identification

Unique Protocol Identification Number
NCT04792528
Brief Title
REACT MCI - Repeated Advanced Cognitive Training in Mild Cognitive Impairment
Acronym
REACT MCI
Official Title
Repeated Advanced Cognitive Training in Mild Cognitive Impairment (The REACT MCI Study). A Randomized, Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 15, 2021 (Actual)
Primary Completion Date
April 15, 2026 (Anticipated)
Study Completion Date
April 15, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sorlandet Hospital HF
Collaborators
Oslo University Hospital, NKS Olaviken, St. Olavs Hospital, NKS Kloverasen, Barrow Neurological Institute, University of Maryland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment
Keywords
computer-based cognitive training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
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.
Allocation
Randomized
Enrollment
213 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
One training period
Arm Type
Experimental
Arm Description
One training period of 30 minutes of daily adaptive training for 4-5 days a week up for 20- 25 trainings using computerized cognitive training.
Arm Title
Two training periods
Arm Type
Experimental
Arm Description
Two training periods of 30 minutes of daily adaptive training for 4-5 days a week up for 20- 25 trainings using computerized cognitive training.
Arm Title
Active control
Arm Type
Active Comparator
Arm Description
The generalized brain training group (Active control) will play solitaire 30 minutes daily for 25 sessions
Intervention Type
Other
Intervention Name(s)
Computerized cognitive training.
Intervention Description
COGMED RM program (Pearson Inc., UK)
Intervention Type
Other
Intervention Name(s)
Generalized brain training / Active control
Intervention Description
Solitaire
Primary Outcome Measure Information:
Title
Working memory training is superior to active control measured by spatial span backwards at 6 months
Time Frame
From enrollment until 6 months
Title
Reduced function in the glymphatic system is associated with reduced working memory training effect measured by CT evaluated craniospinal clearance
Description
Craniospinal clearance will be evaluated with a single CT image scan at level with the foramen magnum.
Time Frame
Enrollment to 12 months
Title
Working memory training impact quality of life measure in the participants as compared to active control measured by EuroQOL5D-5L after 12 months.
Time Frame
Enrollment to12 months
Title
Working memory training prolongs the MCI phase as compared to active controls
Description
We 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.
Time Frame
Enrollment to 48 months
Secondary Outcome Measure Information:
Title
The effect of working memory training is dose related measured by spatial span backwards after 6 months
Time Frame
Enrollment to 6 months
Title
Allelic variations in predefined genetic markes influence training effects after 3 months measured by spatial span backwards.
Description
Allelic 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
Time Frame
Enrollment to 3 months
Title
Workin memory training reduces relatives stress scores as compared to relatives stress scores in the active control group after 12 months
Description
Relatives stress score (RSS) is a validated scale measuring the stress for relatives
Time Frame
Enrollment to 12 months
Title
Working memory training reduces QALY associated cost as compared to active controls at 24 months.
Description
The 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.
Time Frame
Enrollment to 24 months
Title
Working memory training reduces QALY associated cost as compared to active controls at 48 months.
Description
The 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.
Time Frame
enrollment to 48 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 Exclusion Criteria for the REACT MCI Glymphatics substudy: Individuals with known allergy against contrast solutions Individuals with other serious allergies Individuals with kidney failure or glomerular filtration rate < 30 Individuals younger than 18 or older than 80 Pregnant or lactating women For individuals >70 years or with medications affecting kidney function the glomerular filtration rate needs to be less than week old.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mona L Henriksen
Phone
004737075161
Email
mona.lonebu.henriksen@sshf.no
First Name & Middle Initial & Last Name or Official Title & Degree
Susanne S Hernes, M.D. Phd.
Phone
004748136020
Email
Susanne.sorensen.hernes@sshf.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne S Hernes, M.D. Phd.
Organizational Affiliation
Sørlandet Sykehus HF, Universitetet i Bergen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sørlandet Sykehus Arendal
City
Arendal
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susanne L Hernes
Email
Susanne.sorensen.hernes@sshf.no
First Name & Middle Initial & Last Name & Degree
Mona L Henriksen
Facility Name
NKS Olaviken Alderspsykiatriske sykehus - Hukommelsesklinikk
City
Bergen
ZIP/Postal Code
5009
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Minna Hynninen, MD, Phd
Email
kia.minna.johanna.hynninen@olaviken.no
Facility Name
N.K.S. Kløveråsen
City
Bodø
ZIP/Postal Code
8076
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bodil S Olsen
Email
Bol2@kloverasen.no
Facility Name
Oslo Universitetssykehus Ullevål
City
Oslo
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne Brita Knapskog, MD, Phd
Email
Anne-brita@knapskog.net
Facility Name
St. Olavs Hospital
City
Trondheim
ZIP/Postal Code
7006
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rannveig Eldholm, MD, Phd
Email
Rannveig.s.eldholm@ntnu.no

12. IPD Sharing Statement

Plan to Share IPD
No

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REACT MCI - Repeated Advanced Cognitive Training in Mild Cognitive Impairment

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