- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06596720
Acute Effects of Aerobic Exercise on Cognitive Functions in Patients with Chronic Stroke
Evaluating the Immediate Impact of Aerobic Exercise on Cognitive Function in Individuals Affected by Chronıc Stroke
The aim of this observational study is to investigate the acute effects of aerobic exercise on cognitive functions in patients with chronic stroke. The primary question addressed is:
Does aerobic exercise have an impact on cognitive functions in individuals with chronic stroke? Participants with chronic stroke were divided into two groups: those engaging in aerobic exercise and a control group. Both groups underwent cognitive function assessments at intervals of thirty minutes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
WORKPLACE The study was conducted at the Department of Neurological Rehabilitation, Faculty of Physiotherapy and Rehabilitation, Pamukkale University.
PARTICIPANTS The study included 38 stroke patients admitted to Pamukkale University Hospital, aged between 25 and 80, who had a diagnosed cardiopulmonary disease or additional neurological disorders, and did not have defined psychological issues. Individuals with visual or auditory impairments were excluded from the study. Participants were informed about the study, provided with a voluntary information form to read, and written consent was obtained.
In this study, a bicycle ergometer was used considering the safety and individual capabilities of the participants. The protocol consisted of a 5-minute warm-up, 20 minutes of moderate-intensity exercise, and a 5-minute cool-down period. While most studies aim for high-intensity exercise (60-80%), this study focused on a single-session exercise training model; hence, the exercise program for the study group was set at a moderate intensity (40-50%). Participants in the study group wore a pulse oximeter and were instructed to exercise within the specified heart rate ranges. Neuropsychological tests were administered before and after the bicycle ergometer sessions. The control group underwent neuropsychological tests at thirty-minute intervals without using the bicycle ergometer.
REGISTRATION FORM The registration form collected information on demographic data, including the date of stroke onset, medical history, family history, smoking and alcohol use, dominant and affected extremities, and current comorbidities.
ASSESSMENT Participants were randomly assigned to the study or control group using a closed-envelope method. All assessments were conducted in a well-lit and quiet room. Cognitive levels were measured using the Standardized Mini-Mental State Test (SMMT). In the study group, blood pressure, pulse, and oxygen saturation were measured. Subsequently, the Stroop Test T-BAG Form, Letter Cancellation Test, and Wechsler Digit Span Test were administered. After the tests, a thirty-minute submaximal bicycle ergometer session, including a 5-minute warm-up and a 5-minute cool-down period, was conducted. Blood pressure, pulse, and oxygen saturation were measured again, and the tests were repeated. In the control group, blood pressure, pulse, and oxygen saturation were measured before administering the Stroop Test, Letter Cancellation Test, and Wechsler Digit Span Test. To avoid learning effects in the neuropsychological test battery, participants in the control group waited for approximately thirty minutes before repeating cognitive tests, and results were recorded.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Denizli, Turkey
- Pamukkale University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having experienced an ischemic or hemorrhagic stroke
- Having been diagnosed with a stroke at least six months prior
- Having not experienced multiple stroke episodes
- Having no communication difficulties
- Being literate
Exclusion Criteria:
- Having hearing loss
- Receiving additional treatment beyond rehabilitation
- Using a pacemaker
- Presence of cardio-pulmonary disease
- Having experienced a recent trauma
- Having additional neurological disorders aside from stroke
- Having a psychological disorder
- Having a pre-existing condition that affects cognitive level
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study group
Cognitive assessments for participants in the study group were conducted using the Standardized Mini-Mental State Test, Stroop Test T-BAG Form, Wechsler Digit Span subtest, and Letter Cancellation Test.
Participants underwent a thirty-minute session on a moderate-intensity bicycle ergometer.
Subsequently, pulse, oxygen saturation, and blood pressure were measured, and the Stroop Test T-BAG Form, Wechsler Digit Span Tests, and Letter Cancellation Tests were repeated.
|
After the initial assessments of the individuals in the study group were completed, the exercise program was implemented.
The exercise program consisted of 30 minutes of submaximal cycling using the Karvonen formula.
The aerobic exercise program was structured with a 5-minute warm-up, a 5-minute cool-down, and the remaining time dedicated to the exercise phase.
Since our study included only a single exercise session, a moderate-intensity training program was applied to the participants.
|
|
No Intervention: Control group
Cognitive assessments for participants in the control group were conducted using the Standardized Mini-Mental State Test, Stroop Test T-BAG Form, Wechsler Digit Span subtest, and Letter Cancellation Test.
The control group was left in a quiet room for thirty minutes.
After this period, pulse, oxygen saturation, and blood pressure were measured, and the Stroop Test T-BAG Form, Wechsler Digit Span Tests, and Letter Cancellation Tests were repeated
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroop tests
Time Frame: 10 minutes
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This test is a brief measure of selective or focused attention, specifically assessing the ability to shift from one perceptual state to another and suppress response tendencies.
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10 minutes
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Wechsler Forward Digit Span, Wechsler Backward Digit Span
Time Frame: 10 minutes
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This test is used to assess attention and short-term memory.
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10 minutes
|
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CancellationTest
Time Frame: 5 minutes
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This test measures sustained attention, visual scanning, reaction time, and response impulsivity.
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5 minutes
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Saturation
Time Frame: 5 minutes
|
Oxygen saturation indicates the normal level of oxygen transported to tissues.
It is a key indicator, especially for monitoring cardiopulmonary health.
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5 minutes
|
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Pulse values
Time Frame: 5 minutes
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The total number of systolic contractions of the heart per minute is referred to as the heart rate (HR), also known as the pulse.
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5 minutes
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Systolic and diastolic blood pressure
Time Frame: 5 minutes
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Blood pressure refers to the force exerted by blood on the inner walls of the arteries.
It is one of the most fundamental indicators of a person's health.
During ventricular systole, blood is ejected into the arteries, reaching its peak pressure, known as systolic pressure.
During ventricular diastole, blood is drawn back, and the pressure falls to its lowest level, known as diastolic pressure.
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5 minutes
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 60116787-020/46559
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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