CClinicalTrials.gg
Status unknownNCT03619291Updated Aug 7, 2018

High-intensity Functional Circuit Training and Cognitive Function

An interventional study of Aerobic Exercise and High-intensity functional training in Exercise and Cognition, sponsored by Goethe University. Status unknown. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-08-07.

Sponsored by Goethe University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2018), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

The study investigates the acute effects of one bout of high-intensity functional circuit training on cognitive function against no-activity control and aerobic exercise.

Read the detailed description

Exercise has been shown to acutely improve cognitive function (CF). However, it is unknown as to how high-intensity functional circuit training (HIFCT) affects CF. This study aims to compare the acute effects of one HIFCT bout against an inactive control condition as well as against one bout of conventional aerobic exercise.

Healthy participants will be randomly allocated to either a HIFCT group, an aerobic exercise group (walking) or an inactive control group. In the HIFCT group, participants perform a 15-minute workout, which is composed of functional exercise mimicking activities of daily living (e.g. squat, step-ups) and conducted in a circuit format. Each exercise is performed at all-out intensity for 20 seconds, followed by a 10-second break. Thus, the 15-min workout consists of 30 exercise intervals.

In the control group, participants will be inactively seated for 15 minutes, reading sports brochures and literature.

In the walking group, participants will walk at moderate intensity on a treadmill for 15 minutes.

Outcomes assessed pre and post-workout include the stroop test, trail making test, stop-signal task, heart rate, subjective arousal, rate of perceived exertion and exercise enjoyment.

02

Conditions studied

  • Exercise
  • Cognition
03

In context

Lead sponsor

Goethe University is the lead sponsor of 97 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18-40 years

Exclusion criteria

Exclusion Criteria:

  • severe orthopaedic, psychiatric, neurological, endocrine or cardiovascular disorders
  • acute illness, not completely healed injuries
  • muscle soreness
  • pregnancy/nursing period
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    High-intensity functional training

    all-out exercise

    Other: High-intensity functional training

  • Active comparator
    Aerobic exercise

    walking

    Other: Aerobic Exercise

  • Sham comparator
    control

    sitting

    Other: control

Interventions

  • OtherAerobic Exercise

    walking on a treadmill at moderate intensity, total duration 15 minutes

  • OtherHigh-intensity functional training

    functional exercises in circuit format at 20/10 s (work/rest) intervals, total duration 15 minutes

  • Othercontrol

    physical inactivity, reading sports science literature, total duration 15 minutes

06

What researchers measure

Primary outcomes

  1. interference control

    stroop test

    Time frame: 2 min

Secondary outcomes

  1. cognitive flexibility/visual orientation

    trail making test

    Time frame: 2 min

  2. inhibitory control

    stop-signal task

    Time frame: 2 min

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 7, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03619291
Lead sponsor
Goethe University
Responsible party
Prof. Dr. Dr. Winfried Banzer (Prof, Goethe University) — Principal investigator
First posted
Aug 7, 2018
Start date
Aug 2018 (estimated)
Primary completion
Oct 2018 (estimated)
Completion
Nov 2018 (estimated)
Last update
Aug 7, 2018

Study contacts

Jan Wilke, PhD
Contact
wilke@sport.uni-frankfurt.de
0049 69 798 24588
Florian Giesche
Contact
giesche@sport.uni-frankfurt.de
0049 69 79824482

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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