- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01167400
Cybercycling for Cognitive Health
September 4, 2014 updated by: Cay Anderson-Hanley, Union College, New York
Cybercycling for Older Adults: Neuropsychological, Physiological and Behavioral Effects
Exercise has been linked to cognitive health, but few older adults exercise at recommended levels.
Cybercycling may provide additional cognitive benefits due to increased motivation to ride the interactive 3D tours.
Participants will be randomly assigned to three months of either cybercycling or traditional stationary biking; and they will complete comprehensive evaluations before and after exercise.
Older adults are expected to show significant neuropsychological, physiological and behavioral gains.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The purpose of this study is to test the following hypotheses: (1) stationary cycling with virtual reality tours ("cybercyle") will enhance executive function and clinical status more than traditional exercise; (2) exercise effort will explain improvement; and (3) brain-derived neurotrophic growth factor (BDNF) will increase.
Study Type
Interventional
Enrollment (Actual)
63
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Colonie, New York, United States, 12222
- Beltrone Living Center
-
Malta, New York, United States, 12065
- Highpointe Apartments
-
Niskayuna, New York, United States, 12308
- Glen Eddy
-
Saratoga Springs, New York, United States, 12866
- Prestwick Chase
-
Saratoga Springs, New York, United States, 12866
- Wesley Health Care (Woodlawn and Embury)
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Saratoga Springs, New York, United States, 12866
- Westview Apartments
-
Schenectady, New York, United States, 12308
- Schaffer Heights
-
Schenectady, New York, United States, 12308
- Kingsway Village
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age 50+
- able to participate in cycling
- physician permission
Exclusion Criteria:
- unstable heart condition
- physician denial
- neurological condition
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cybercycling
cybercycling for 3 months
|
exercising on a videogame-enhanced interactive 3D stationary bicycle for 3 months, 3-5x/wk
Other Names:
|
|
Active Comparator: Traditional Stationary Biking
Traditional exercise on a stationary bike for 3 months.
|
exercising on a traditional stationary bike for 3 months, 3-5x/wk
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in cognitive function after three months of exercise.
Time Frame: 3 months
|
Cognitive function, especially executive function, will be assessed before and after three months of either cybercycling or traditional exercise biking.
Neuropsychological tests will assess: cognitive flexibility and simultaneous processing(i.e., Stroop, Digits Backwards, and Trails Difference Score).
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight
Time Frame: 3 months
|
Weight and other physiological factors will be assessed before and after 3 months of exercise.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Cay Anderson-Hanley, PhD, Union College
- Principal Investigator: Paul Arciero, DPE, Skidmore College
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2008
Primary Completion (Actual)
August 1, 2010
Study Completion (Actual)
August 1, 2010
Study Registration Dates
First Submitted
July 20, 2010
First Submitted That Met QC Criteria
July 21, 2010
First Posted (Estimate)
July 22, 2010
Study Record Updates
Last Update Posted (Estimate)
September 5, 2014
Last Update Submitted That Met QC Criteria
September 4, 2014
Last Verified
September 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HS1259
- 64449 (Other Grant/Funding Number: Robert Wood Johnson Foundation)
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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