- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04861818
The Role of the Time of Day in the Effects of Exercise on Memory in Heathy Young Adults (TEEMY)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cumulative evidence indicates that a single bout of exercise has beneficial impacts on short- and long-term memory in young adults. From a physiological perspective, acute exercise leads to changes of heart rate variability (HRV), which is associated with memory retrieval process. From a psychological perspective, acute exercise increases the arousal level and thus facilitates cognitive processing including memory storage and retrieval. Such HRV- and/or arousal-based effects of exercise on memory could be differed by the time of day in young adults based on their circadian rhythms of HRV; sleep-wake transition led to rapid changes of HRV. Moreover, young adults prefer afternoon or evening to morning, showing less wakefulness and lower memory performance in the morning relative to afternoon. Based on the potential physiological and/or psychological mechanisms, exercise could impact young adults' memory differently by the time of day. Few studies, however, tested the effects of exercise on memory based on the time of day; rather, a recent study found null effects of exercise-induced arousal on implicit and explicit memory performance in college students in the morning.
The investigators here aim to 1) determine the extent to which the time of day moderates how moderate-intensity cardiovascular exercise impacts verbal-auditory and visuo-spatial short- and long-term memory in young adults, and 2) consider potential physiological and psychological markers that may mediate exercise's effects on cognitive performance. Specifically, the investigators will conduct a mixed-design randomized experiment to compare the effects of a single session of moderate-intensity cardiovascular exercise on cognitive performance at two times of day - in the morning (7 - 9 AM) and late afternoon (3 - 5 PM). Participants in each of two groups (morning versus afternoon) will complete two sessions of cognitive tests - at baseline without exercise and after an exercise intervention, while their emotional states, arousal levels, and heart rate (HR) will be measured at baseline, before, during, and after the exercise and memory sessions. The hypotheses are 1) acute exercise in the morning will be more beneficial for short- and long-term memory than an equal volume of exercise in the afternoon; 2) resting HRV and changes in perceived arousal and emotional states will be associated with memory performance following the exercise intervention. The rationale for the hypotheses is that cognitive benefits of exercise can differ by the preference for the time of day, so it is important to investigate such interactions to inform recommendations of the timing of exercise for young adults in academic settings. Moreover, exploring the role of psychophysiological markers in mediating exercise effects on cognition help to further understanding of the benefits of exercise for brain health.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shin Park, PhD
- Phone Number: 336-256-1069
- Email: k_park4@uncg.edu
Study Locations
-
-
North Carolina
-
Greensboro, North Carolina, United States, 27412
- Recruiting
- UNC Greensboro
-
Contact:
- Kyounshin Park, PhD
- Phone Number: 336-256-1069
- Email: k_park4@uncg.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Between the ages of 18-25.
- Currently meeting the American College of Sports Medicine's recommended guidelines of activity (at least 90 min/week of moderate and/or vigorous physical activity).
- Willing to participate for 4 days (2 visits) and refrain from exercise outside of the lab for 4 days (1 day before and the day of two visits).
Exclusion Criteria:
- Any known history of cardiac, pulmonary, or metabolic disease (e.g. cardiovascular disease, asthma, diabetes).
- A current musculoskeletal injury, mental illness (e.g., depression, anxiety, or stress disorders), or sleep disorder.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Morning group
Participant are assigned to the morning group (7-9am) for 30-min exercise/rest interventions.
|
Eligible participants will come into the lab on day 1 and 3 at the same time of day (either morning at 7-10am or afternoon at 3-5pm).
They will be then randomly assigned for a rest or an exercise session prior to the memory test.
For the rest condition, they will be required to sit and relax while watching Planet Earth for 30 minutes on a cycle ergometer.
During the exercise session, they will complete a moderate-intensity cardiovascular exercise for 20 minutes following a 5-min warm-up and followed by a 5-min cool-down on a cycle ergometer.
They will start the memory test immediately after the rest/exercise session.
|
|
Experimental: Afternoon group
Participant are assigned to the afternoon group (3-5pm) for 30-min exercise/rest interventions.
|
Eligible participants will come into the lab on day 1 and 3 at the same time of day (either morning at 7-10am or afternoon at 3-5pm).
They will be then randomly assigned for a rest or an exercise session prior to the memory test.
For the rest condition, they will be required to sit and relax while watching Planet Earth for 30 minutes on a cycle ergometer.
During the exercise session, they will complete a moderate-intensity cardiovascular exercise for 20 minutes following a 5-min warm-up and followed by a 5-min cool-down on a cycle ergometer.
They will start the memory test immediately after the rest/exercise session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Verbal episodic memory change
Time Frame: Immediately after the intervention, the first cognitive test
|
Verbal episodic memory will be assessed immediately and 24 hour after intervention (rest and exercise) using the Auditory Verbal Learning Test (AVLT trial 1 - 8; max/min score: 15/0 for each trial)
|
Immediately after the intervention, the first cognitive test
|
|
Visual episodic memory change
Time Frame: Immediately after the intervention, the second cognitive test
|
Verbal episodic memory will be assessed immediately after intervention (rest and exercise) using the NIH Toolbox Picture Sequence Memory Test (max/min score: 30/0).
|
Immediately after the intervention, the second cognitive test
|
|
Lure discrimination index change
Time Frame: Immediately after the intervention, the third cognitive test
|
Lure discrimination index will be assessed immediately after intervention (rest and exercise) using the Mnemonic Similarity Task (max/min score: 1/0).
|
Immediately after the intervention, the third cognitive test
|
|
Working memory change
Time Frame: Immediately after the intervention, the fourth cognitive test
|
Verbal episodic memory will be assessed immediately after intervention (rest and exercise) using the Digits Span Forward and Backward Task (max/min score: 14/0).
|
Immediately after the intervention, the fourth cognitive test
|
Collaborators and Investigators
Investigators
- Principal Investigator: Kyoung Shin Park, PhD, UNC Greensboro
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- 20-0141
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
product manufactured in and exported from the U.S.
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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