Effects of Dual-task Aerobic Exercise
Acute Effect of Dual-task Aerobic Exercise on Cognitive Load and Myocardial Oxygen Consumption in Healthy Sedentary Individuals
1 other identifier
interventional
34
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 7, 2024
CompletedFirst Posted
Study publicly available on registry
June 14, 2024
CompletedStudy Start
First participant enrolled
July 7, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 16, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2024
CompletedDecember 17, 2024
December 1, 2024
1 month
June 7, 2024
December 12, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
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.
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 Outcomes (1)
Reaction time evaluation
Time to acute change in measurements 1 hour before the application and 1 hour after the application.
Study Arms (2)
Double leg dual duty aerobic exercise group
EXPERIMENTALDuring 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.
Double leg standard aerobic exercise group
ACTIVE COMPARATORIn 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.
Interventions
Group of people doing dual tasks during double-leg cycling training.
The group that received only aerobic exercise.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Istanbul Medipol University Hospitallead
- University of Yalovacollaborator
- Istanbul Gedik Universitycollaborator
Study Sites (1)
Ebrar Atak
Yalova, 77100, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof.
Study Record Dates
First Submitted
June 7, 2024
First Posted
June 14, 2024
Study Start
July 7, 2024
Primary Completion
August 16, 2024
Study Completion
September 30, 2024
Last Updated
December 17, 2024
Record last verified: 2024-12