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

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

      • Yalova, Turkey, 77100
        • Ebrar Atak

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.
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.
The group that received only aerobic exercise.

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).
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.
Time to acute change in measurements 1 hour before the application and 1 hour after the application.

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

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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