- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06461130
Effects of Dual-task Aerobic Exercise
December 12, 2024 updated by: ebrar atak, Istanbul Medipol University Hospital
Acute Effect of Dual-task Aerobic Exercise on Cognitive Load and Myocardial Oxygen Consumption in Healthy Sedentary Individuals
The aim of this study was to examine the acute effect of dual-task aerobic exercise on cognitive load and myocardial oxygen consumption in healthy sedentary individuals.
In this study: 1.
Does dual-task exercise applied in addition to aerobic training have an acute effect on cognitive load in healthy sedentary individuals?
2. Does dual-task exercise applied in addition to aerobic training in healthy sedentary individuals have an acute effect on myocardial oxygen consumption, which reflects the indirect oxygen consumption of the heart?
The questions were answered.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
To find answers to the questions of the study, healthy sedentary participants were randomized into two groups by online randomization method.
One of the groups was the group that received only double-leg aerobic exercise.
The other group was the double-leg aerobic exercise group integrated with dual-task-oriented training.
Before and after the interventions, the blood pressure and pulse rate of the participants were measured, their cognitive functions were evaluated with the MOCA Test, their reaction times were evaluated with the Nelson Reaction Test, and the acute effect of the trainings was examined.
Study Type
Interventional
Enrollment (Actual)
34
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
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Yalova, Turkey, 77100
- Ebrar Atak
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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:
- Volunteering to participate in the study
- No comorbidities
- Absence of comorbid diseases of the orthopedic, neurological, cardiopulmonary system
- Participants who have not been involved in another clinical trial in the last 1 month
Exclusion Criteria:
- Participants who had hip, pelvis, knee, ankle surgery in the last year
- Sensory loss
- Participants with leg length inequality
- Participants with known balance disorders in the last three months due to vestibular disorders, pregnancy, concussion
- Presence of systemic disease (diabetes, blood pressure, etc.)
- Those using bronchodilator drugs
- Having a neurological disease
- Not being in good psychological condition
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Double leg dual duty aerobic exercise group
During double-leg cycling training, people were made to do dual tasks.
Dual-task: aerobic training on a bicycle ergometer + serial sevens In the dual-task condition, participants completed the exercise while simultaneously performing a series of sevens cognitive tasks.
Specifically, participants were instructed to serially subtract sevens from a prescribed three-digit number (range 100-300) and read the calculations aloud while performing aerobic exercise.
|
Group of people doing dual tasks during double-leg cycling training.
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|
Active Comparator: Double leg standard aerobic exercise group
In double leg cycling training, both legs; Exercise was performed on the bicycle ergometer, starting with a 5-minute warm-up (25% labor force) on the ergometer before the application, lasting a total of 20 minutes, and continuously training at 70% intensity.
Finished with 5 minutes of cooling.
Individuals were allowed to maintain a pedaling frequency of 50 rpm, set externally with a metronome.
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The group that received only aerobic exercise.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cognitive load assessment
Time Frame: Time to acute change in measurements 1 hour before the application and 1 hour after the application.
|
Cognitive load change was assessed with the Montreal Cognitive Function Assessment Scale (MOCA).
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Time to acute change in measurements 1 hour before the application and 1 hour after the application.
|
|
Myocardial oxygen consumption assessment
Time Frame: Time to acute change in measurements 1 hour before the application and 1 hour after the application.
|
Myocardial oxygen consumption was calculated using the Double Product formula of the data obtained from blood pressure and pulse measurement.
|
Time to acute change in measurements 1 hour before the application and 1 hour after the application.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction time evaluation
Time Frame: Time to acute change in measurements 1 hour before the application and 1 hour after the application.
|
Reaction time was determined by measuring the distance the ruler caught after the ruler was released.
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Time to acute change in measurements 1 hour before the application and 1 hour after the application.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
July 7, 2024
Primary Completion (Actual)
August 16, 2024
Study Completion (Actual)
September 30, 2024
Study Registration Dates
First Submitted
June 7, 2024
First Submitted That Met QC Criteria
June 11, 2024
First Posted (Actual)
June 14, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 12, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DualTaskwithAerobicTraining
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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