Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2015-08-31
2016-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
PREVENTION
NONE
Study Groups
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High Intensity Interval Training/FitBit Flex
Meet with personal trainer once per week for 20-minute exercise session
High Intensity Interval Training
High Intensity Interval Training
FitBit Flex
Use to measure increase in Physical Activity
Moderate Intensity/FitBit Flex
Meet with personal trainer once per week for 30-minute exercise session and exercise two times a week outside of personal trainer
Moderate Intensity
Moderate Intensity Training
FitBit Flex
Use to measure increase in Physical Activity
Delayed Control/FtBit Flex
No exercise offered
Delayed Control
Delayed Control
FitBit Flex
Use to measure increase in Physical Activity
Interventions
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High Intensity Interval Training
High Intensity Interval Training
Moderate Intensity
Moderate Intensity Training
Delayed Control
Delayed Control
FitBit Flex
Use to measure increase in Physical Activity
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* stable physical/mental health,
* current smoker
* currently minimally active,
* ambulatory,
* interested in increasing their physical activity,
* willingness to attend weekly exercise intervention sessions at a SNAP Fitness location within 10 miles of the University of Minnesota campus,
* the ability to comply with the study protocol and provide informed consent
Exclusion Criteria
* abnormal electrocardiogram or V02 test results,
* high blood pressure (defined as systolic blood pressure over 165 or diastolic blood pressure over 100),
* heart attack, acute (2 days) cardiac event or stroke in preceding six months,
* unstable angina,
* uncontrolled dysrhythmias causing hemodynamic compromise,
* symptomatic severe aortic stenosis,
* uncontrolled symptomatic heart failure,
* acute pulmonary embolism or pulmonary infarction,
* acute myocarditis or
* pericarditis,
* dissecting aneurism,
* acute systemic infection and
* unstable pulmonary or cardiovascular conditions.
18 Years
40 Years
ALL
Yes
Sponsors
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University of Minnesota
OTHER
Responsible Party
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Principal Investigators
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Alicia Allen, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Minnesota
Locations
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DCRU
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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1505m70321
Identifier Type: -
Identifier Source: org_study_id
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