Effects of Dual-task Aerobic Exercise

Sedentary Behavior Clinical Trial

Official title:

Acute Effect of Dual-task Aerobic Exercise on Cognitive Load and Myocardial Oxygen Consumption in Healthy Sedentary Individuals

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06461130
• Other study ID #: DualTaskwithAerobicTraining
• Status: Completed
• Phase: N/A
• Start date: September 10, 2023
• Est. completion date: May 30, 2024

Study information

• Verified date: June 2024
• Source: Istanbul Medipol University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: May 30, 2024
• Est. primary completion date: May 16, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 40 Years

Eligibility

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

Related Conditions & MeSH terms

• Sedentary Behavior

Intervention

Other:
• Study Group
Group of people doing dual tasks during double-leg cycling training.
• Control Group
The group that received only aerobic exercise.

Locations

Country	Name	City	State
Turkey	Ebrar Atak	Yalova

Sponsors (3)

Lead Sponsor	Collaborator
Istanbul Medipol University Hospital	Istanbul Gedik University, University of Yalova

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cognitive load assessment	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.
Primary	Myocardial oxygen consumption assessment	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	Reaction time evaluation	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.