- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04680494
Effect of Acute Physical Exercise on Memory (SPEMO)
An increasing amount of studies show the beneficial effect of regular exercise on cognitive and brain functions and especially in the memory domain. Yet little is known of what happens within an acute bout of exercise and whether it would also yield cognitive effects. The literature clearly shows that molecules such as brain derived neurotrophic factor (BDNF) and endocannabinoids (mainly anandamide, AEA) are heavily involved in neural plasticity mechanisms and increase when we exercise hinting at possible mechanisms underlying memory improvement after exercise.
This protocol assesses the effects of acute exercise on associative and motor sequence memory, their underlying neural activations (measured using fMRI) and blood biomarkers (BDNF and AEA). A related aim is to assess the effect of exercise intensity, therefore three exercising conditions (rest, moderate intensity and high intensity) were included. Finally, a 3-month delayed retest visit is also realized to assess effects of acute exercise on long-term memory consolidation.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male
- Right-handed,
- Exercising regularly (at least twice per week).
- VO2max comprised between 40ml/kg/min and 65ml/kg/min.
Exclusion Criteria:
- Psychiatric and neurological history
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Rest
Participants rest quietly for 30 minutes, sitting on a chair.
They may read magazines not involving motion-related elements
|
|
|
EXPERIMENTAL: Moderate intensity exercise
Participants cycle on a cycle ergometer during 30 minutes at 65% of their maximal cardiac frequency
|
|
|
EXPERIMENTAL: High intensity exercise
Participants cycle on a cycle ergometer during 15 minutes at 75% of their maximal cardiac frequency.
This session also includes 3 minutes of warm-up and three minutes of cool down at 50% of their maximal cardiac frequency
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
cognitive measures - performance
Time Frame: Till the end of the study for each participant, i.e.3 months (long time retest)
|
we measure performance during cognitive tasks.
Performance is measured as percentage of correct trials, with higher percentages corresponding to better performance - measured in percentages.
|
Till the end of the study for each participant, i.e.3 months (long time retest)
|
|
cognitive measures - reaction times
Time Frame: Till the end of the study for each participant, i.e.3 months (long time retest)
|
we measure reaction times during cognitive tasks.
For reaction times, lower measures correspond to faster response times and therefore to better outcome - measured in milliseconds.
|
Till the end of the study for each participant, i.e.3 months (long time retest)
|
|
BDNF levels
Time Frame: up to 1 hour
|
we measure BDNF levels before and after physical exercise and rest, measured in ng/mL of serum.
|
up to 1 hour
|
|
endocannabinoid levels
Time Frame: up to 1 hour
|
we measure endocannabinoid levels before and after physical exercise and rest, measured in ng/mL of plasma.
|
up to 1 hour
|
|
brain activations
Time Frame: up to 1 hour
|
we measure brain activations using fMRI during cognitive tasks
|
up to 1 hour
|
Collaborators and Investigators
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PB_2017-00360
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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