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Acute Cycling on Executive Control (ACE)

W

Western University, Canada

Status

Completed

Conditions

Physical Activity

Treatments

Behavioral: High-Intensity Cycling
Behavioral: Light-Intensity Cycling
Behavioral: Moderate-Intensity Cycling
Behavioral: Sitting

Study type

Interventional

Funder types

Other

Identifiers

NCT03499977
PA and Executive Functioning

Details and patient eligibility

About

This study will examine whether 10-minute bouts of cycling at various intensities will impact executive functioning (i.e., cognitive ability) as assessed by the antisaccade (AS) task through a total of five visits. An antisaccade is a rapid eye movement away from a visual target. The ability to suppress making an eye movement towards a visual target gauges inhibitory control (i.e., a domain of executive functioning). In the initial visit, participants' exercise capacity will be assessed through a maximal effort cycling test. Intensities for the cycling bouts (i.e., high, moderate, low) in subsequent sessions will be based upon this maximal effort cycling test. In visits 2 through 5, participants will complete an AS task, followed by a 10-minute bout of cycling, and then complete the AS task again. The order of cycling intensities will be randomized between participants. Differences in the AS task (i.e., reaction time and accuracy) will be compared between and within cycling conditions.

Enrollment

20 patients

Sex

All

Ages

18 to 64 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to read, write and understand English
  • Full time student enrolled at Western University
  • Able to perform a ten-minute exercise task at a light intensity without health implications
  • Have email or phone number for contacting purposes

Exclusion criteria

  • Do not have a medical condition that prevents you from exercise (e.g. heart attack in the past year, heart disease, irregular heartbeat, etc.)
  • Do not have history of eye injury or neurological impairment
  • Do not have an orthopaedic limitation
  • Are not pregnant

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

20 participants in 4 patient groups

Sitting
Experimental group
Description:
The participant will be asked to sit for 10 min (not increasing their heart rate) then do the anti-saccade task
Treatment:
Behavioral: Sitting
Low-Intensity Cycling
Experimental group
Description:
Participant will be asked to cycle for 10 min (\<40% VO2R) and then perform the anti-saccade task
Treatment:
Behavioral: Light-Intensity Cycling
Moderate-Intensity Cycling
Experimental group
Description:
The participant will be asked to do 10 min of cycling (40-59% VO2R) followed but the anti-saccade task
Treatment:
Behavioral: Moderate-Intensity Cycling
High-Intensity Cycling
Experimental group
Description:
The participant will be asked to do 10 min of cycling (60%-84% VO2R) followed but the anti-saccade task
Treatment:
Behavioral: High-Intensity Cycling

Trial contacts and locations

1

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Central trial contact

Harry Prapavessis, Ph.D; Kirsten B Dillon, B.Sc

Data sourced from clinicaltrials.gov

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