NCT02746692

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P50-P75 for not_applicable healthy

Timeline
Completed

Started Jul 2016

Typical duration for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 18, 2016

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 21, 2016

Completed
2 months until next milestone

Study Start

First participant enrolled

July 1, 2016

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2017

Completed
Last Updated

November 30, 2017

Status Verified

November 1, 2017

Enrollment Period

1.1 years

First QC Date

April 18, 2016

Last Update Submit

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

EXPERIMENTAL
Other: Fit15

Comparison

ACTIVE COMPARATOR
Other: Endurance

Interventions

Fit15OTHER

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

Intervention

Moderate intensity ergometer training. Total duration 50 minutes

Comparison

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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

Locations