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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02527876
Other study ID # 1505m70321
Secondary ID
Status Withdrawn
Phase N/A
First received August 5, 2015
Last updated January 22, 2018
Start date August 2015
Est. completion date October 2016

Study information

Verified date January 2018
Source University of Minnesota - Clinical and Translational Science Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate how physical activity levels change in young adults when they start a specific exercise program.


Description:

The purpose of this study is to evaluate how physical activity levels change in young adults when they start a specific exercise program. Physical activity levels will be monitored daily via a FitBit Flex. Outcome measures include number of minutes of activity per day and distance traveled per day.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- 18-40 years old,

- 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:

- Contraindications to increasing physical activity including, but not limited to,

- 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
High Intensity Interval Training
High Intensity Interval Training
Moderate Intensity
Moderate Intensity Training
Delayed Control
Delayed Control
Device:
FitBit Flex
Use to measure increase in Physical Activity

Locations

Country Name City State
United States DCRU Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota - Clinical and Translational Science Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With Increase in Physical Activity as assessed by FitBit 12 weeks