- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02746692
Faster Back Home: Efficacy of a High-intensity Endurance Training (Fit15)
Faster Back Home: a Randomized Controlled Equivalence Study on the Efficacy of a High-intensity 15 Minute Aerobic Endurance Training
Sports medical experts recommend considerable amounts of regular physical activity in order to improve strength, motor control, endurance and flexibility. However, only a small share of the population is able to meets the corresponding international guidelines. One reason for this is supposed to consist in private scheduling problems and the high time expenditure. Against this background, high-intensity intermittent training methods with short durations have become popular.
The present study aims to evaluate the effectivity of a high -intensity functional circuit training (the FIT15 program) in improving body function.
Thirty healthy individuals will be included in the randomized, controlled two-armed parallel group trial. In the intervention group, the participants will perform the FIT15 program, a group-based high-intensity circuit training based on functional movement patterns (e.g. squats, push-ups, burpees, jumps, rope-skipping). The training will be carried out three times a week, each 15 minutes for a total of six weeks. In the control group, the participants will exercise three times a week (in total for six weeks) at moderate intensity on an ergometer according to the cardiopulmonary exercise guidelines of the American College of Sports Medicine. Outcomes assess prior and following the six-week training period encompass body fat and muscle mass (bio impedance analysis), aerobic exercise capacity (spirometric exercise testing including lactate analysis), postural control (force plate), maximum strength of the leg extensors and shoulder muscles (1 repetition maximum) and psychometric variables (e.g. physical activity readiness questionnaire).
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hessen
-
Frankfurt/Main, Hessen, Germany, 60487
- Department of Sports Medicine, Goethe University Frankfurt/Main
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- healthy
- subscribing informed consent
Exclusion Criteria:
- Drug intake in the past 48 hours
- Pregnancy
- Muscle soreness
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
|
Group-based high-intensity circuit training based on functional movement patterns (e.g. squats, push-ups, burpees, jumps, ropeskipping). Total duration 15 minutes circle training: 20s workout, 10 rest |
|
Active Comparator: Comparison
|
Moderate intensity ergometer training.
Total duration 50 minutes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Maximal ventilatory aerobic endurance capacity assessed by spiroergometry
Time Frame: 10 min.
|
10 min.
|
|
Maximal lactate aerobic endurance capacity assessed by spiroergometry
Time Frame: 10 min.
|
10 min.
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Jumping performance; counter movement jump
Time Frame: 1 min.
|
1 min.
|
|
Dynamic balance assessed with the time to stabilization test
Time Frame: 2 min
|
2 min
|
|
Static balance assessed with the time to stabilization test
Time Frame: 2 min
|
2 min
|
|
Maximal isometric voluntary force of the shoulder muscles
Time Frame: 10 min
|
10 min
|
|
Maximal isometric voluntary force of the lower limb extensors
Time Frame: 10 min
|
10 min
|
|
body composition assessed with a external non-invasive impedance device
Time Frame: 10 min.
|
10 min.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SpM2016-003
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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