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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06461130
Other study ID # DualTaskwithAerobicTraining
Secondary ID
Status Completed
Phase N/A
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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.
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