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ExerciseNCT03619291

High-intensity Functional Circuit Training and Cognitive Function

A study testing Aerobic Exercise and High-intensity functional training in people with Exercise and Cognition, run by Goethe University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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 more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Exercise, Cognition
What is being tested?
Aerobic Exercise and High-intensity functional training
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
36 participants
Where
No sites listed yet
Study dates
Aug 2018to Nov 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 18-40 years

Who cannot join

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

Trial locations and contacts

No sites are listed yet.

About this study

Official title: Acute Effects of High-intensity Functional Circuit Training on Cognitive Function: a Randomised, Controlled Trial

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.

Conditions
Exercise, Cognition
Being tested
Aerobic Exercise, High-intensity functional training, control
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Aerobic ExerciseOther

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

  • High-intensity functional trainingOther

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

  • controlOther

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

Study groups in NCT03619291
Study groupRoleWhat they receive
High-intensity functional trainingExperimentalall-out exercise
Receives: Other: High-intensity functional training
Aerobic exerciseActive comparatorwalking
Receives: Other: Aerobic Exercise
controlSham comparatorsitting
Receives: Other: control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. interference control

    stroop test

    Measured: 2 min

Secondary outcomes (2)
  1. cognitive flexibility/visual orientation

    trail making test

    Measured: 2 min

  2. inhibitory control

    stop-signal task

    Measured: 2 min

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Aug 2018
  2. Study startAug 2018 (estimated)
  3. Primary completionOct 2018 (estimated)
  4. Study completionNov 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
36 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03619291
Sponsor's protocol ID
SpM2018-001
Status last verified
Aug 2018
First submitted
27 Jul 2018
Last updated
7 Aug 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Aerobic Exercise and High-intensity functional training in people with Exercise and Cognition, run by Goethe University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 7 Aug 2018. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Jan Wilke, PhD (0049 69 798 24588, wilke@sport.uni-frankfurt.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

interference control (time frame: 2 min). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Aug 2018; AzTrials last refreshed its copy on 2 Nov 2026.

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