NCT06461130

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
34

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 14, 2024

Completed
23 days until next milestone

Study Start

First participant enrolled

July 7, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 16, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2024

Completed
Last Updated

December 17, 2024

Status Verified

December 1, 2024

Enrollment Period

1 month

First QC Date

June 7, 2024

Last Update Submit

December 12, 2024

Conditions

Keywords

dual taskaerobic trainingcardiovascularcognition

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

EXPERIMENTAL

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.

Other: Study Group

Double leg standard aerobic exercise group

ACTIVE COMPARATOR

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.

Other: Control Group

Interventions

Group of people doing dual tasks during double-leg cycling training.

Double leg dual duty aerobic exercise group

The group that received only aerobic exercise.

Double leg standard aerobic exercise group

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Ebrar Atak

Yalova, 77100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Sedentary Behavior

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

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

Locations