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
1 other identifier
interventional
40
1 country
1
Brief Summary
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy
Started Jul 2016
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 18, 2016
CompletedFirst Posted
Study publicly available on registry
April 21, 2016
CompletedStudy Start
First participant enrolled
July 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2017
CompletedNovember 30, 2017
November 1, 2017
1.1 years
April 18, 2016
November 28, 2017
Conditions
Outcome Measures
Primary Outcomes (2)
Maximal ventilatory aerobic endurance capacity assessed by spiroergometry
10 min.
Maximal lactate aerobic endurance capacity assessed by spiroergometry
10 min.
Secondary Outcomes (6)
Jumping performance; counter movement jump
1 min.
Dynamic balance assessed with the time to stabilization test
2 min
Static balance assessed with the time to stabilization test
2 min
Maximal isometric voluntary force of the shoulder muscles
10 min
Maximal isometric voluntary force of the lower limb extensors
10 min
- +1 more secondary outcomes
Study Arms (2)
Intervention
EXPERIMENTALComparison
ACTIVE COMPARATORInterventions
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
Eligibility Criteria
You may qualify if:
- healthy
- subscribing informed consent
You may not qualify if:
- Drug intake in the past 48 hours
- Pregnancy
- Muscle soreness
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Sports Medicine, Goethe University Frankfurt/Main
Frankfurt am Main, Hesse, 60487, Germany
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of Department
Study Record Dates
First Submitted
April 18, 2016
First Posted
April 21, 2016
Study Start
July 1, 2016
Primary Completion
August 1, 2017
Study Completion
August 1, 2017
Last Updated
November 30, 2017
Record last verified: 2017-11