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Clinical Trials/NCT03479177
NCT03479177
Completed
Not Applicable

The Effect of a Home-Based High Intensity Interval Training Intervention on Increasing Exercise Among Low Active Adults

University of Minnesota1 site in 1 country50 target enrollmentJuly 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
University of Minnesota
Enrollment
50
Locations
1
Primary Endpoint
Exercise minutes per week
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to examine the effect of a home-based high intensity interval training intervention on exercise among low active adults (defined as engaging in exercise 90 minutes or less per week). Participants will be randomly assigned to a HIIT-based intervention or a wait-list control each lasting 12 weeks (participants in the wait-list control condition will have the option of receiving the HIIT intervention following the 12 weeks).

Detailed Description

The intervention will be a 12-week high intensity interval training workout that will consist of home-based exercise sessions prescribed by the exercise counselor. The exercise sessions will be based on exercises the participant can confidentially engage in (regular push-ups vs. knee push-ups vs. wall push-ups). The goal will be to engage in three exercise sessions per week. The participants will receive weekly telephone calls during the first month and bi-weekly calls during months 2 and 3. The exercise counselor will also engage in dialogue that will motivate the participant to exercise.

Registry
clinicaltrials.gov
Start Date
July 1, 2018
End Date
September 1, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 and older
  • Exercising for 90 minutes or less each week
  • Access to the Internet

Exclusion Criteria

  • A history of coronary heart disease (history of myocardial infarction, symptoms of angina)
  • Orthopedic problems that would limit physical activity participation
  • Osteoarthritis
  • Any other medical condition that may make physical activity unsafe or unwise.
  • Current or planned pregnancy
  • Psychosis or current suicidal ideation
  • Psychiatric hospitalization within the last six months

Outcomes

Primary Outcomes

Exercise minutes per week

Time Frame: Change from Baseline to 12 weeks

Exercise minutes per week as assessed by an accelerometer for one week at baseline and 12 weeks. Higher reported minutes per week indicates a higher level of physical activity.

Secondary Outcomes

  • Physical Activity Self-efficacy Questionnaire(Change from Baseline to 12 weeks)
  • Biometrics(Change from Baseline to 12 weeks)
  • Social Support for Exercise Questionnaire(Change from Baseline to 12 weeks)
  • Physical Activity Enjoyment Scale (PACES)(Change from Baseline to 12 weeks)
  • Outcome Expectancies Questionnaire(Change from Baseline to 12 weeks)

Study Sites (1)

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