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Clinical Trials/NCT06461130
NCT06461130
Completed
Not Applicable

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

Istanbul Medipol University Hospital1 site in 1 country34 target enrollmentJuly 7, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sedentary Behavior
Sponsor
Istanbul Medipol University Hospital
Enrollment
34
Locations
1
Primary Endpoint
Myocardial oxygen consumption assessment
Status
Completed
Last Updated
last year

Overview

Brief 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.

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.

Registry
clinicaltrials.gov
Start Date
July 7, 2024
End Date
September 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Medipol University Hospital
Responsible Party
Principal Investigator
Principal Investigator

ebrar atak

Asst. Prof.

University of Yalova

Eligibility Criteria

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

Outcomes

Primary Outcomes

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.

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).

Secondary Outcomes

  • Reaction time evaluation(Time to acute change in measurements 1 hour before the application and 1 hour after the application.)

Study Sites (1)

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