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Clinical Trials/NCT06340659
NCT06340659
Recruiting
N/A

Concurrent Aerobic Exercise and Cognitive Training to Prevent Alzheimer's in At-risk Older Adults (The Exergames Telerehabilitation Study)

University of Minnesota1 site in 1 country104 target enrollmentAugust 14, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
At Risk for AD-dementia, With Subjective Cognitive Decline
Sponsor
University of Minnesota
Enrollment
104
Locations
1
Primary Endpoint
fluid cognition (global cognition)
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

Significance of Research Question/Purpose: Subjective cognitive decline (SCD) is regarded as the first clinical manifestation in the AD-dementia continuum and currently has a prevalence of 11.2% in adults over the age of 45, with incidence increasing with greater age. Furthermore, population-based studies suggest that between 50% and 80% of older individuals (aged 70 years and older) who perform normally on cognitive tests, report some form of perceived decline in cognitive functioning when asked. The SCD state is unique as this population is more likely than their healthy peers to present with AD biomarkers such as neurodegeneration and amyloid burden, and therefore represents probable preclinical AD relative to other causes of SCD. Likewise, growing evidence suggests that a significant proportion of those adults are subsequently found to develop MCI, or AD, following the classic SCD-MCI-AD trajectory, with SCD increasing MCI risk 1.5-3 fold. Preventing Alzheimer's disease (AD) is arguably the most important approach to address the dementia epidemic worldwide because 99.6% of drug trials failed and no drugs can yet prevent, cure, or even slow AD. A treatment that delays the onset of AD by five years could save $89 billion in 2030.This highlights an urgent and pressing need to develop behavioral interventions to prevent AD and slow its progression.

This study will use a randomized, 2-parallel group, trial design that is guided by the Consolidated Standards of Reporting Trials (CONSORT)and the SPIRIT checklist. We will randomize 104 community-dwelling older adults to one of two arms for 3 months: home-based (asynchronous telerehabilitation) Exergame (HbExergame) or home-based (asynchronous telerehabilitation) aerobic exercise (HbAEx). Randomization will allocate subjects on a 1:1 allocation ratio within each age stratum (65-74 and >75), and will use permuted blocks of 8 and 4. We do not expect equal numbers of subjects in each age stratum, but want to balance the groups for each age. Investigators will be blinded to group assignment. All participants will be blinded to study aims and reminded as needed not to discuss their experiences with outcome assessors. Outcome assessors (also blinded to group allocations) will measure: 1) feasibility (attendance, adherence to exercise dose, systems usability scale), 2) preliminary cognition: fluid cognition [primary outcome], attention, episodic memory, and processing speed [secondary outcomes] using the NIH Toolbox cognition battery and aerobic fitness [VO2peak and 6-minute walk distance], and 3) blood neurotrophic biomarkers.

Registry
clinicaltrials.gov
Start Date
August 14, 2024
End Date
September 30, 2026
Last Updated
8 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Cognitive complaint (defined as answering yes to the questions's "Do you perceive memory or cognitve difficulties?" and "In the last two years, has your cognition or memory declined?";
  • Montreal Cognitive Assessement (MoCA) 26 or greater
  • Age 65 years and older;
  • English-speaking;
  • Without ACSM contraindication to exercise

Exclusion Criteria

  • Dementia or mild cognitive impairment diagnosis;
  • Neurological or major psychiatric disorder, alcohol/chemical dependency or recent medical condition (anethesia COVID-19 \["brain fog"\]) likely causing cognitive impairment;
  • Current enrollment in another intervention study

Outcomes

Primary Outcomes

fluid cognition (global cognition)

Time Frame: 12 weeks

which refers to the overall cognitive ability and will be assessed with the NIH Toolbox Cognitive Battery (NIHTB-CB) and its Fluid Composite Score (convergent validity \[r = 0.78\] and test-retest reliability \[r = 0.86)

Secondary Outcomes

  • Aerobic fitness(12 weeks)
  • Neuroprotective biomarkers and ApoE status.(12 weeks)
  • Depressive Symptoms(12 weeks)
  • Exergame-specific usability and satisfaction(12 weeks)
  • Anxiety Symptoms(12 weeks)
  • SCD Symptoms(12 weeks)

Study Sites (1)

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