Skip to main content
Clinical Trials/NCT02527876
NCT02527876WithdrawnNot Applicable

Exercise to Promote Quit Attempts in Young Adults

University of Minnesota2 sites in 1 countryStarted: August 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
2
Primary Endpoint
Number of Participants With Increase in Physical Activity as assessed by FitBit

Study Overview

Brief Summary

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

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

High Intensity Interval Training/FitBit Flex

Experimental

Meet with personal trainer once per week for 20-minute exercise session

Intervention: High Intensity Interval Training (Behavioral)

High Intensity Interval Training/FitBit Flex

Experimental

Meet with personal trainer once per week for 20-minute exercise session

Intervention: FitBit Flex (Device)

Moderate Intensity/FitBit Flex

Experimental

Meet with personal trainer once per week for 30-minute exercise session and exercise two times a week outside of personal trainer

Intervention: Moderate Intensity (Behavioral)

Moderate Intensity/FitBit Flex

Experimental

Meet with personal trainer once per week for 30-minute exercise session and exercise two times a week outside of personal trainer

Intervention: FitBit Flex (Device)

Delayed Control/FtBit Flex

Placebo Comparator

No exercise offered

Intervention: Delayed Control (Behavioral)

Delayed Control/FtBit Flex

Placebo Comparator

No exercise offered

Intervention: FitBit Flex (Device)

Outcomes

Primary Outcomes

Number of Participants With Increase in Physical Activity as assessed by FitBit

Time Frame: 12 weeks

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

Loading locations...

Similar Trials

Exercise, Activity and Smoking in Young... | Clinical Trial