- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04848038
Combined Exercise Trial (COMET)
Differential Effects of Exercise Modality on Cognition and Brain in Older Adults
Study Overview
Detailed Description
Older adults often experience physical decline that can be directly ameliorated by physical activity and exercise. Evidence is building that exercise prevents cognitive decline or delays the onset of debilitating dementia (e.g. Alzheimer's disease) yet, the optimal dose and combination of exercise modalities for promoting brain health, however, remains unknown and essentially untested.
The long-term research goal of this project is to develop and test strategies to support successful aging and prevent Alzheimer's disease. The study will enroll 280 individuals, age 65 to 80 years without cognitive impairment, into a 26-week exercise intervention to test the combined and independent effects of aerobic and resistance training on cognition, brain structure, and physical function. The project will also explore underlying biological mechanisms that may link exercise with brain health.
Participants will be randomized into 1 of 4 groups: flexibility, toning and balance (control), aerobic exercise training, progressive resistance training, or combined aerobic and resistance training. All intervention groups represent the most common modalities of exercise and directly reflect the public health recommendations for aerobic and resistance training. Exercise training will occur in a community setting through the network of Greater Kansas City Young Men's Christian Association. It is hypothesized that 26 weeks of exercise will improve 1) cognitive performance, 2) regional brain volume, 3) cardiorespiratory fitness and strength 4) biomarkers.
This will be the largest study to assess the combined and independent effects of the two most recommended forms of exercise. Demonstrating specific exercise effects on cognitive function and brain health in older adults would have enormous public health implications. The study's results will also impact public health policy and education by providing evidence towards the specific or synergistic effects of aerobic and resistance training on cognition and brain structure. Encouraging the public to adapt more active lifestyles and stimulate the development of effective exercise delivery programs to enhance initiation and maintenance of physical activity interventions is key to increasing the number of quality years of life for America's aging population.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kansas
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Fairway, Kansas, United States, 66205
- University of Kansas Alzheimer's Disease Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 65-80 yrs (inclusive at time of consent).
- Conversant English speaking and reading ability.
- Medical clearance by a health care provider.
- Reliable means of transportation.
- Telephone Interview of Cognitive Status score > 25 and adjudication of normal cognition based on cognitive test data by a study medical monitor.
Exclusion Criteria:
- Intention to move out of the area or travel for more than 4 weeks in the next year.
- Use of an assistive device for ambulation.
- Joint pain severe enough to prevent taking walks in community, lifting objects over your head due to pain or restriction of movement, or that is worsened by increasing physical activity.
- Any MRI contraindications or refusal to attempt MRI.
- Treatment for alcohol or substance abuse in the last 2 years.
- Treatment for cancer (other than non-metastatic, localized cancer) in the last 2 years.
- Currently taking insulin.
- Diagnosis of heart disease, heart failure, heart attack, or heart surgery or chest pain with effort in the last 2 years.
- Untreated atrial fibrillation, valve replacements, angioplasty or stent placement in the last 2 years regardless of physician clearance.
- History of major psychiatric illness including schizophrenia (not including general anxiety disorder or depression), multiple sclerosis, Parkinson's, Dementia, mild cognitive impairment, brain injury (traumatic or clinically evident Stroke), or similar, likely to negatively impact cognitive testing.
- Head injury with loss of consciousness for more than a few minutes.
- Change in blood pressure medication in the last 2 months.
- Considered "Active" or engaging in a progressive resistance training 2 or more times a week.
- reported condition likely to compromise ability to safely perform exercise as determined by study medical monitor (e.g. chronic obstructive pulmonary disease, Lupus, end stage renal disease, etc.)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Core and Fusion Training
150 minutes/week of Core and Fusion exercise, a mix of low impact toning, strengthening, flexibility and balance exercises.
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Standard public health exercise recommendations
Other Names:
|
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Active Comparator: Endurance Training
Moderate-intensity endurance training such as brisk walking, 150 minutes/week over 3-5 days.
Progression based on a set schedule.
In addition 0-2 days of Core and Fusion control exercise will also be recommended.
|
Standard public health exercise recommendations
Other Names:
|
|
Active Comparator: Weight Training
Progressive resistance training 2 days/week, non-consecutive, of 2 sets (10 - 15 repetitions) of 10 exercises (~75 minutes/week).
Progression based on repetition completion and 1-repetition maximum.
In addition 3 days of Core and Fusion control exercise will also be recommended.
|
Standard public health exercise recommendations
Other Names:
|
|
Active Comparator: Combined Endurance and Weight Training
Moderate-intensity endurance training such as brisk walking, 150 minutes/week over 3-5 days.
Progression based on a set schedule.
Progressive resistance training 2 days/week, non-consecutive, of 2 sets (10 - 15 repetitions) of 10 exercises (~75 minutes/week).
Progression based on repetition completion and 1-repetition maximum.
|
Standard public health exercise recommendations
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Global Cognition
Time Frame: Baseline, 6 months, 12 months
|
Assessing change in cognitive function from baseline to 12 months.
The 6 month measure is being used to assess the trajectory of the change.
A comprehensive neuropsychological battery will be used that assesses a global cognition score derived from domains of cognition (e.g.
Executive Function, Visuospatial Processing, Episodic Memory, Processing Speed).
We will use a second order confirmatory factor analysis (CFA) to estimate the factor loadings between the observed indicators and the first order factors and between the first and second order factors.
The CFA will use baseline data to avoid any potential intervention related biases.
The primary outcome will be constructed by summing the weighted average (by the estimated first and second order loadings) of the standardized observed scores across the cognitive tests.
|
Baseline, 6 months, 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hippocampal volume
Time Frame: Baseline, 12 months
|
Volume of bilateral hippocampus in milliliters
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Baseline, 12 months
|
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Peak oxygen consumption
Time Frame: Baseline, 12 months
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Peak volume of oxygen used in in milliliters per kilogram of body mass per minute during a graded maximal exercise test
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Baseline, 12 months
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1-Repetition Maximum
Time Frame: Baseline, 12 months
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The maximum amount of mass that can be lifted one time (summed leg press and chest press)
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Baseline, 12 months
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hopkins Verbal Learning Test - Revised
Time Frame: Baseline, 6 months, 12 months
|
The Hopkins Verbal Learning Test - Revised is an oral test that has been validated within brain-disordered populations (e.g., Alzheimer's disease, amnestic disorders) as a measure of verbal learning and memory.
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Baseline, 6 months, 12 months
|
|
NIH Toolbox Flanker Task
Time Frame: Baseline, 6 months, 12 months
|
The NIH ToolboxFlanker Task is a computer based test to assess selective attention and inhibitory function.
|
Baseline, 6 months, 12 months
|
|
NIH Toolbox Dimensional Change Card Sort
Time Frame: Baseline, 6 months, 12 months
|
The NIH Toolbox Dimensional Change Card Sort is a computer based test to assess cognitive flexibility and attention.
|
Baseline, 6 months, 12 months
|
|
NIH Toolbox Oral Symbol Digit Test
Time Frame: Baseline, 6 months, 12 months
|
The NIH Toolbox Oral Symbol Digit Test is a computer based test to Measure of processing speed.
|
Baseline, 6 months, 12 months
|
|
Virginia Cognitive Aging Project Logical Memory
Time Frame: Baseline, 6 months, 12 months
|
The Virginia Cognitive Aging Project Logical Memory test measures episodic verbal memory.
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Baseline, 6 months, 12 months
|
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Letter Comparison
Time Frame: Baseline, 6 months, 12 months
|
This paper-based task measures processing speed.
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Baseline, 6 months, 12 months
|
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Matrix Reasoning
Time Frame: Baseline, 6 months, 12 months
|
This computer-based task measures visuospatial ability.
|
Baseline, 6 months, 12 months
|
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Task Switching
Time Frame: Baseline, 6 months, 12 months
|
This computer task asks participants to learn two different tasks.
This task measures task switching.
|
Baseline, 6 months, 12 months
|
|
Spatial Working Memory
Time Frame: Baseline, 6 months, 12 months
|
This computer task measures spatial memory.
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Baseline, 6 months, 12 months
|
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Stroop Task
Time Frame: Baseline, 6 months, 12 months
|
This paper-based oral task measures executive control, specifically attention and inhibitory control.
|
Baseline, 6 months, 12 months
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Fat Mass
Time Frame: Baseline, 12 months
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Estimated total body, axial, appendicular and visceral fat mass from dual x-ray absorptiometry.
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Baseline, 12 months
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Lean Mass
Time Frame: Baseline, 12 months
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Estimated total body, axial, appendicular lean mass from dual x-ray absorptiometry.
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Baseline, 12 months
|
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Bone Mass
Time Frame: Baseline, 12 months
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Estimated total body, axial, appendicular bone mass and density from dual x-ray absorptiometry.
|
Baseline, 12 months
|
|
Cerebral brain blood flow
Time Frame: Baseline, 12 months
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Whole brain and regional cerebral blood flow estimated using arterial spin labeling, a technique of magnetic resonance imaging
|
Baseline, 12 months
|
|
Senior Fitness Test
Time Frame: Baseline, 12 months
|
Composite and sub-test scores of 6 common physical activities.
Scores can be normalized for age and sex
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Baseline, 12 months
|
|
Waist to Hip Ratio
Time Frame: Baseline, 12 months
|
The circumference of the waist and hip areas are measured via measuring tape.
|
Baseline, 12 months
|
|
Body Mass Index
Time Frame: Baseline, 12 months
|
Height and body mass are measured and Body Mass Index is calculated based on a standard equation.
|
Baseline, 12 months
|
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Blood lactate concentration
Time Frame: Baseline, 12 months
|
Blood lactate concentration is measured before and after a bout of exercise.
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Baseline, 12 months
|
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Pittsburgh Sleep Quality Index
Time Frame: Baseline, 6 months, 12 months
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Paper-based questionnaire of self-rated sleep quality.
|
Baseline, 6 months, 12 months
|
|
Perceived Stress Scale, 10-item
Time Frame: Baseline, 6 months, 12 months
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Paper-based questionnaire of self-rated appraisal of stress.
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Baseline, 6 months, 12 months
|
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National Health and Nutrition Examination Survey Diet Survey Questionnaire
Time Frame: Baseline, 6 months, 12 months
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Self-rated computer based questionnaire of dietary intake.
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Baseline, 6 months, 12 months
|
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Mediterranean Eating Pattern for Americans
Time Frame: Baseline, 6 months, 12 months
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Self-rated computer based questionnaire of mediterranean diet eating pattern.
|
Baseline, 6 months, 12 months
|
|
Barriers Self-Efficacy Scale
Time Frame: Baseline, 3 months, 6 months, 12 months
|
Self-rated computer based questionnaire of physical activity self-efficacy.
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Baseline, 3 months, 6 months, 12 months
|
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Exercise Self-Efficacy Scale
Time Frame: Baseline, 3 months, 6 months, 12 months
|
Self-rated computer based questionnaire of exercise goal self-efficacy.
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Baseline, 3 months, 6 months, 12 months
|
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Leisure Self-Efficacy Scale
Time Frame: Baseline, 3 months, 6 months, 12 months
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Self-rated computer based questionnaire of leisure-time physical activity self-efficacy.
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Baseline, 3 months, 6 months, 12 months
|
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Godin Leisure-Time Exercise Questionnaire
Time Frame: Baseline, 3 months, 6 months, 12 months
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Self-rated computer based measure of use of leisure-time for physical activity
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Baseline, 3 months, 6 months, 12 months
|
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Wechsler Test of Adult Reading
Time Frame: Baseline
|
The Wechsler Test of Adult Reading is a reading recognition test that can be used to estimate intelligence quotient and memory scores
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Baseline
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Spatial Relations
Time Frame: Baseline, 26-weeks, 52-weeks
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In this computer task, participants are asked to determine which three-dimensional figure can be formed from a two-dimensional pattern presented.
This task measures visual construction ability.
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Baseline, 26-weeks, 52-weeks
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MacArthur Scale of Subjective Social Status
Time Frame: Baseline, 6 months, 12 months
|
The MacArthur Scale of Subjective Social Status (MacArthur Socio-Economic Status Scale) contains questions regarding finances, assets and other home socioeconomics.
|
Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Applied Cognitive Abilities v1.0
Time Frame: Baseline, 6 months, 12 months
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Computer-based adaptive questionnaire of self-rated cognitive function.
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Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Applied Cognitive General Concerns v1.0
Time Frame: Baseline, 6 months, 12 months
|
Computer-based adaptive questionnaire of self-rated cognitive concerns.
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Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety v1.0
Time Frame: Baseline, 6 months, 12 months
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Computer-based adaptive questionnaire of self-rated anxiety.
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Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Depression v1.0
Time Frame: Baseline, 6 months, 12 months
|
Computer-based adaptive questionnaire of self-rated depression.
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Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Ability to Participate in Social Roles and Activities v1.0
Time Frame: Baseline, 6 months, 12 months
|
Computer-based adaptive questionnaire of self-rated social roles.
|
Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) General Life Satisfaction v1.0
Time Frame: Baseline, 6 months, 12 months
|
Computer-based adaptive questionnaire of self-rated life satisfaction.
|
Baseline, 6 months, 12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function v1.0
Time Frame: Baseline, 6 months, 12 months
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Computer-based adaptive questionnaire of self-rated life physical function.
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Baseline, 6 months, 12 months
|
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EuroQol Group Five Dimension Five Level (EQ-5D-5L)
Time Frame: Baseline, 6 months, 12 months
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A visual analog scale of quality of life
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Baseline, 6 months, 12 months
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Physical Activity Self-Regulation Scale, 12-item
Time Frame: Baseline, 3 months, 6 months, 12 months
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Self-rated computer based measure of physical activity self-regulation for use with older adults.
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Baseline, 3 months, 6 months, 12 months
|
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Blood biomarkers
Time Frame: Baseline, 6 months, 12 months
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Brain Derived Neurotrophic factor , Insulin Growth Factor-1 (IGF-1), lactate, glucose and insulin levels, inflammatory cytokines, plasma phosphorylated tau (various form), plasma beta-amyloid (various forms), neurofilament light, glial fibrillary acidic protein and others as become available.
|
Baseline, 6 months, 12 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Eric D Vidoni, PhD, University of Kansas Medical Center
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 146904
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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