Effects of a Bicycling Intervention on Cognitive Skills and Cardiovascular Health (BIKE)
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| ClinicalTrials.gov Identifier: NCT02453178 |
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Recruitment Status :
Completed
First Posted : May 25, 2015
Last Update Posted : January 30, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Sedentary Lifestyle | Behavioral: Cycling | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 33 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Basic Science |
| Official Title: | Effects of a Bicycling Intervention on Cognitive Skills and Cardiovascular Health |
| Study Start Date : | July 2015 |
| Actual Primary Completion Date : | January 2018 |
| Actual Study Completion Date : | January 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Steady state moderate intensity cycling
Moderate intensity exercise training will be a 12-week supervised cycling program, with supervision directly from our research team. All participants will first receive a one-on-one orientation with an exercise training specialist that has been trained by Dr. Gary Pierce in monitoring an exercise program for healthy older adults. Training will start with a 5 minute-warm-up, 20 minutes moderate intensity cycling and 30 minutes passive cycling, and 5 minute cool-down per session, for 3 sessions/week. In each additional week, we will add 6 minutes of moderate intensity cycling per session, until the total time for moderate intensity is 50 minutes per session by the start of week 5 (with additional 5 minute warm-up and 5 minute cool-down).
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Behavioral: Cycling
The experimental group will complete a 3 month exercise program that includes working up to cycling at a moderate intensity for 50 minutes/session 3 times a week. The comparison group will complete a 3-month exercise program that includes intermittent cycling (alternating between passive and moderate intensity) for 50 minutes/session 3 times a week. Both groups will exercise in our laboratory at Spence Labs, and will be supervised by an exercise trainer that is trained in working with elderly and special populations.
Other Name: Exercise |
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Active Comparator: Intermittent cycling
The intermittent cycling group will come to the exercise lab for the same duration and frequency each week and complete primarily passive cycling such that a motor in the stationary bicycle moves the pedals for them. To maintain interest in this intervention, we will include short bouts of moderate intensity activity. The short bouts of moderate intensity cycling will be designed to be ineffective for substantially increasing cardiorespiratory fitness over the course of the intervention.
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Behavioral: Cycling
The experimental group will complete a 3 month exercise program that includes working up to cycling at a moderate intensity for 50 minutes/session 3 times a week. The comparison group will complete a 3-month exercise program that includes intermittent cycling (alternating between passive and moderate intensity) for 50 minutes/session 3 times a week. Both groups will exercise in our laboratory at Spence Labs, and will be supervised by an exercise trainer that is trained in working with elderly and special populations.
Other Name: Exercise |
- Functional brain network integrity: the strength of the correlation between fluctuating functional magnetic resonance imaging (fMRI) signal in different brain regions of the Default Mode Network (DMN) and the Executive Control Network (ECN) at rest [ Time Frame: Change from baseline functional network integrity at 12-weeks ]Resting state brain networks known to be vulnerable to decline with normal aging
- Motor learning rate [ Time Frame: Change from baseline learning rate at 12-weeks ]Learning rate parameter expressing rate of reaction time speeding in an alternating serial reaction time task (ASRTT)
- Explicit paired associates learning rate [ Time Frame: Change from baseline learning rate at 12-weeks ]Learning rate parameter expressing rate of improvement in accuracy in a paired associates learning task
- Executive function composite measure [ Time Frame: Change from baseline executive function performance at 12-weeks ]Composite score from performance (speed and accuracy) on four executive function tasks, including Trails A and B, Go/No-Go dual task, a modified flanker task, and a non-verbal working memory n-back task
- Cardiovascular fitness measured as "Vo2 max" from a cycle ergometer test [ Time Frame: Change from baseline fitness at 12-weeks ]The ability of the heart and lungs to supply oxygen to working muscle tissues and the ability of the muscles to use oxygen to produce energy for movement
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 60 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Eligible to participate in an aerobic exercise intervention based on the Physical Activity Readiness Questionnaire, and corrected vision of 20/40.
- Because our older adult sample is over the age of 40, we will also require completion of a detailed health history questionnaire and further eligibility for the exercise intervention will be determined following approval from a physician that monitored electrocardiography (ECG) response during a maximal aerobic fitness test that is part of the second study visit described below.
Exclusion Criteria:
- Not between the ages of 60 and 80 years old
- Not fluent in English
- Score < 26 (out of 30) on the Montreal Cognitive Assessment (MoCA)
- Inability to comply with experimental instructions
- Qualify as "high risk" for acute cardiovascular event by the published standards of the American College of Sports Medicine
- Left-handed
- Previous diagnosis of neurological, metabolic, or psychiatric condition, and no previous brain injury associated with loss of consciousness
- Inability to complete an MRI
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02453178
| United States, Iowa | |
| HBC Lab | |
| Iowa City, Iowa, United States, 52245 | |
| Principal Investigator: | Michelle Voss, PhD | University of Iowa |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Michelle W. Voss, Assistant Professor of Psychological and Brain Sciences, University of Iowa |
| ClinicalTrials.gov Identifier: | NCT02453178 |
| Other Study ID Numbers: |
201405837 |
| First Posted: | May 25, 2015 Key Record Dates |
| Last Update Posted: | January 30, 2018 |
| Last Verified: | January 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | In accord with NIH regulations, we will make the data and relevant documentation available to other investigators at their request upon acceptance of the main findings from the study for publication. Because the collected data are to remain anonymous, only a subject number will identify all data. To further protect the privacy and confidentiality of the data, data and documentation will be made available only under a data-sharing agreement that provides for restrictions for the transferring of data to others and a commitment that the data will be used for research purposes only and not for a profit-making enterprise. |
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physical activity aging cognition brain exercise |

