The Effects of Exercise Timing and Intensity on Motor Learning in Healthy Adults.

December 11, 2023 updated by: Muhammed Şeref Yıldırım, Trakya University

Effects of a Single Bout of Low and Moderate Intensity Aerobic Exercise on Acquisition and Retention of Motor Learning in Young Adults

The purpose of this study is to compare of the effects of a single session of aerobic exercise with different intensity and timing on motor learning processes in healthy young adults.

Study Overview

Detailed Description

Long-term aerobic training are associated with improved motor learning. Recent studies have shown that even a single bout of moderate or high ıntensity aerobic exercise can lead to immediate improvements on motor learning. On the other hand, there is still insufficient knowledge about whether aerobic exercise should occur before or after motor practice and what the intensity of aerobic exercise should be. In this study, the ınvestigators examined the effects of a single bout of low and moderate intensity aerobic exercise applied before or after motor practice on golf putting task. Additionally, the ınvestıgators evaluated the effects of sleep quality on motor learning and the acute effects of the exercise on cognition. 75 young adults were divided into five groups: two groups that did low or moderate intensity aerobic exercise before motor practice (LOW-MP, MOD-MP), two groups that did aerobic exercise after motor practice (MP-LOW, MP-MOD), and non-exercise control group. The acquisition practice consisted of six blocks of ten golf puttings. The retention was also evaluated both 1 day and 7 days after the experimental day with one block each. The putting performance was measured with accuracy and consistency error scores were computed for each acquisition and retention block. The sleep quality of the night before and the experimental day were evaluated using the Richard Campbell Sleep Scale.

Study Type

Interventional

Enrollment (Actual)

75

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • İskender
      • Edirne, İskender, Turkey, 22100
        • Faculty of Health Science, Trakya University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 18-24 years
  • Risk score less than two based on The American Heart Association (AHA) and American College of Sports Medicine (ACSM) health/fitness facility pre-participation screening questionnaire
  • Physical activity level>1500 MET/min weeks based on the International Physical Activity Questionnaire (IPAQ)

Exclusion Criteria:

  • being elite athletes
  • being smokers
  • using psychiatric/neurologic medications.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: MP-LOW (pre-motor practice (MP) low ıntensity aerobic exercise )

On the experimental day, they participated in 60 golf puttings (acquisition practice) followed by a half-hour low-intensity treadmill run.

Retention levels were measured 1 and 7 days after the experimental day with 10 puttings each.

Sleep quality (richard campbell sleep questionnaire) and cognitive level (Paced auditory serial addition test) were evaluated in all participants.

The exercise intervention was 30 min of treadmill jogging/running. After a two-minute warm-up walk at 1.0 m/s, the treadmill speed was increased to 57-63% maximum heart rate.
Experimental: MP-MOD (pre-motor practice (MP) moderate ıntensity aerobic exercise )

On the experimental day, they participated in 60 golf puttings (acquisition practice) followed by a half-hour moderate-intensity treadmill run.

Retention levels were measured 1 and 7 days after the experimental day with 10 puttings each.

Sleep quality (richard campbell sleep questionnaire) and cognitive level (Paced auditory serial addition test) were evaluated in all participants.

The exercise intervention was 30 min of treadmill jogging/running. After a two-minute warm-up walk at 1.0 m/s, the treadmill speed was increased to 64-76% maximum heart rate.
Experimental: MOD-MP (post-motor practice (MP) moderate ıntensity aerobic exercise )

On the experimental day, they participated in a half-hour moderate-intensity treadmill run followed by 60 golf puttings (acquisition practices).

Retention levels were measured 1 and 7 days after the experimental day with 10 puttings each.

Sleep quality (richard campbell sleep questionnaire) and cognitive level (Paced auditory serial addition test) were evaluated in all participants.

The exercise intervention was 30 min of treadmill jogging/running. After a two-minute warm-up walk at 1.0 m/s, the treadmill speed was increased to 64-76% maximum heart rate.
Experimental: LOW-MP ((post-motor practice (MP) low ıntensity aerobic exercise )

On the experimental day, they participated in a half-hour low-intensity treadmill run followed by 60 golf puttings (acquisition practices).

Retention levels were measured 1 and 7 days after the experimental day with 10 puttings each.

Sleep quality (richard campbell sleep questionnaire) and cognitive level (Paced auditory serial addition test) were evaluated in all participants.

The exercise intervention was 30 min of treadmill jogging/running. After a two-minute warm-up walk at 1.0 m/s, the treadmill speed was increased to 57-63% maximum heart rate.
No Intervention: Control

On the experimental day, they completed 60 golf puttings (just acquisition practices- NO EXERCISE) Retention levels were measured 1 and 7 days after the experimental day with 10 puttings each.

Sleep quality (richard campbell sleep questionnaire) and cognitive level (Paced auditory serial addition test) were evaluated in all participants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Bivariate variable error score (BVE)
Time Frame: For each of 8 golf putting blocks (6 acquisition blocks on the experimental day, 1 retention block 1 day after the experimental day and 1 retention block 7 days after the experimental day
The distance of the ball to the target in the x- and y-coordinates was recorded for each putting with the help of coordinate lines drawn on the artificial grass mat. Recorded coordinates were used to calculate the bivariate variable error (BVE) scores. The BVE, also referred to as consistency, was measured, as the average of the absolute distance to the subject's own midpoint. Each subject's midpoint was measured as the average hit location over ten puttings for each block. Lower BVE indicates greater consistency.
For each of 8 golf putting blocks (6 acquisition blocks on the experimental day, 1 retention block 1 day after the experimental day and 1 retention block 7 days after the experimental day
Median Radial Error (MRE)
Time Frame: For each of 8 golf putting blocks (6 acquisition blocks on the experimental day, 1 retention block 1 day after the experimental day and 1 retention block 7 days after the experimental day
The distance of the ball to the target in the x- and y-coordinates was recorded for each putting with the help of coordinate lines drawn on the artificial grass mat. Recorded coordinates were used to calculate the Median Radial Error (MRE) scores. The mean radial error (MRE) was measured as the average of the absolute distances to the centre of the target of the 10 shots comprising each block.
For each of 8 golf putting blocks (6 acquisition blocks on the experimental day, 1 retention block 1 day after the experimental day and 1 retention block 7 days after the experimental day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Paced auditory serial addition task (PASAT)
Time Frame: For the four exercise groups: On the experimental day 2 times immediately before and after the half-hour exercise For control group: immediately before and after the half-hour rest.
The PASAT is a measure of cognitive function that assesses auditory information processing speed and working memory, as well as calculation ability. The PASAT is presented using recording tape to ensure standardization in the rate of stimulus presentation. Single digits are presented every 2 seconds and the patient must add each new digit to the one immediately prior to it. The score for the PASAT is the total number correct out of 60 possible answers.
For the four exercise groups: On the experimental day 2 times immediately before and after the half-hour exercise For control group: immediately before and after the half-hour rest.
Richard Campbell Sleep Questionnaire (RCSQ)
Time Frame: Day 1 (experimental day) and Day 2 (1 day retention visit)
The RCSQ is a five-item self-report questionnaire that is used in order to assess perceived sleep depth, sleep latency (time to fall asleep), and number of awakenings, as well as sleep efficiency and quality.
Day 1 (experimental day) and Day 2 (1 day retention visit)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Muhammed Ş Yıldırım, PhD, Trakya University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 12, 2022

Primary Completion (Actual)

October 4, 2022

Study Completion (Actual)

October 4, 2022

Study Registration Dates

First Submitted

December 3, 2023

First Submitted That Met QC Criteria

December 3, 2023

First Posted (Actual)

December 12, 2023

Study Record Updates

Last Update Posted (Estimated)

December 18, 2023

Last Update Submitted That Met QC Criteria

December 11, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • TU-FTR-MŞY-001

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I can share my data with all participants who contact me by e-mail.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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