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Aerobic Exercise for Alzheimer's Disease (BIMII Trial)

N/A
Recruiting
Led By Marc J Poulin, PhD, DPhil
Research Sponsored by University of Calgary
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
Not fluent in verbal and written English
History of stroke
Timeline
Screening 3 weeks
Treatment Varies
Follow Up participants will be assessed at 6, 12 and 18 months.
Awards & highlights
No Placebo-Only Group

Summary

This trial tests whether regular aerobic exercise can help prevent dementia in older adults with memory issues. The exercise program aims to improve brain health by boosting blood flow and fitness. Researchers hope to show that this can slow down or prevent cognitive decline.

Who is the study for?
This trial is for inactive adults aged 50-80 with memory complaints but no dementia, and at least one vascular risk factor like high blood pressure or diabetes. They should not be doing vigorous exercise more than twice a week and must speak English fluently. People with serious illnesses, history of stroke, or other conditions that could affect the study can't join.
What is being tested?
The trial tests if regular aerobic exercise can prevent or slow down cognitive decline in older adults at risk of Alzheimer's Disease and related dementias (ADRD). Participants will do either aerobic exercises or stretching-toning exercises to see which helps brain health and cognition more.
What are the potential side effects?
While the trial focuses on beneficial effects, potential side effects from increased physical activity may include muscle soreness, fatigue, joint pain, and an elevated risk of injury. The intensity will be monitored to minimize these risks.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am not fluent in English.
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I have had a stroke in the past.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~participants will be assessed at 6, 12 and 18 months.
This trial's timeline: 3 weeks for screening, Varies for treatment, and participants will be assessed at 6, 12 and 18 months. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Change in Blood Biomarkers Assessed by Elisa Assays
Change in Health behaviour with appropriate support strategies
Change in Maximal Oxygen Uptake (VO2max) Assessed by Metabolic Cart
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Stretch and StrengthExperimental Treatment1 Intervention
A control group will meet on a similar schedule as the exercise group for sessions on stretching and toning but without aerobic exercise. Based on prior RCTs of similar interventions the investigators expect this control to be ineffective or minimally effective, but anticipate that it will increase participant enthusiasm and retention. All assessments will be conducted in this arm.
Group II: Aerobic exerciseExperimental Treatment1 Intervention
Participants will take part in a supervised 6-month-long aerobic (walk/jog) training program held 3 days/week. Each session will include a 5-min warm-up, 20-40 min of aerobic exercise (walking, jogging), 5-min cool-down, and stretching. Exercise prescriptions will follow current principles and guidelines established by ACSM/AHA, including sufficient warm-up, cool-down, and ongoing provision of safety precautions/exercise tips. As participants progress, the duration of aerobic exercise will increase from 20 (month 1) to 30 (months 2-3) and 40 min (months 4-6), with proportional increases to warm-up and cool-down periods. Exercise intensity will be based on individual maximal oxygen uptake (VO2 max), measured at baseline. Intensity will build from 30-45% (months 1-3) to mitigate the risk of injury and will progress to 60-70% (months 4-6) heart rate reserve (HRR).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Aerobic exercise
2000
Completed Phase 2
~1130

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Aerobic exercise is believed to improve cognitive function in dementia patients by enhancing vascular function and cerebrovascular reserve. This is achieved through increased cerebral blood flow and better regulation of blood vessels in the brain, which can mitigate age-related declines in brain health. These improvements are crucial for dementia patients as they help maintain cognitive performance and potentially slow the progression of cognitive decline. Additionally, aerobic exercise may influence molecular and cellular changes, such as reducing inflammation and promoting neurogenesis, further supporting brain health.
Exercise as Potential Therapeutic Target to Modulate Alzheimer's Disease Pathology in APOE ε4 Carriers: A Systematic Review.Galantamine for vascular cognitive impairment.

Find a Location

Who is running the clinical trial?

Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,388 Previous Clinical Trials
26,517,809 Total Patients Enrolled
16 Trials studying Dementia
1,278,729 Patients Enrolled for Dementia
University of CalgaryLead Sponsor
809 Previous Clinical Trials
886,125 Total Patients Enrolled
5 Trials studying Dementia
1,040 Patients Enrolled for Dementia
Marc J Poulin, PhD, DPhilPrincipal InvestigatorUniversity of Calgary
3 Previous Clinical Trials
322 Total Patients Enrolled

Media Library

Aerobic exercise Clinical Trial Eligibility Overview. Trial Name: NCT03035851 — N/A
Dementia Research Study Groups: Aerobic exercise, Stretch and Strength
Dementia Clinical Trial 2023: Aerobic exercise Highlights & Side Effects. Trial Name: NCT03035851 — N/A
Aerobic exercise 2023 Treatment Timeline for Medical Study. Trial Name: NCT03035851 — N/A
~30 spots leftby Nov 2025