- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05744765
Effects of Breathing Exercises on Reaction Time (reaction time)
Short And Long Term Effects Of Breathing Exercises on Reaction Time: A Randomized Controlled Trial
Study Overview
Detailed Description
A total of 40 participants who volunteered to participate in the study from the students of the Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Bandırma Onyedi Eylül University will be included in the study. Participants will be randomly divided into two groups using a simple random numbers table. The study group (15 people) will be given respiratory exercises (12 sessions). The control group (15 people) will receive no intervention. In the study, after the demographic characteristics of the participants are obtained, reaction time will be evaluated with auditory and visual reaction tests and upper extremity reaction tests. All evaluations are planned to take a total of 15 minutes.
The same assessments will be performed in both groups. To measure the long-term effect, after the initial evaluations are completed, the study group will be given a total of 12 sessions of breathing exercises for 4 weeks (3 days a week). After 4 weeks, both groups will be evaluated again. To measure the short-term effect, the respiratory exercise program will be started after the 1st evaluation in the study group, and the 2nd evaluation will be made after the first session.
Canan Demir will perform breathing exercises, and the other researchers who will evaluate will not know which group the participants are in. In this way, the study will be single-blinded.
Translated with www.DeepL.com/Translator (free version)
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Balıkesir, Turkey, 10200
- BandırmaOnyediEylulU
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Volunteering to participate in the study
- To be between the ages of 18-30
- Not having any problems that prevent breathing exercises
Exclusion Criteria:
- Acute infection or chronic disease of neurological, psychiatric, orthopedic, cardiological, rheumatological, etc. origin
- Having had any injury and/or operation (trauma, surgery, fracture, etc.) in the last 6 months
- Regular medication use
- Presence of respiratory disease (asthma, COPD, etc...)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Breathing exercises
First evaluation - breathing exercises (1 session) - second evaluation - breathing exercises (11 sessions) - third evaluation
|
After the initial 5 minutes of relaxed breathing, the participants will perform diaphragmatic and costal breathing for 10 minutes.
.5 diaphragmatic breathing will be done in 1 minute.
|
|
No Intervention: No exercise
First evaluation - no intervention (1 session) - second evaluation - no intervention (11 sessions) - third evaluation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Finger reaction test
Time Frame: 4weeks
|
By placing the dominant hand index finger on the left button of a computer mouse, the participant will be asked to press the left button as soon as the traffic light pattern glows green on the screen.
|
4weeks
|
|
Upper extremity reaction test
Time Frame: 4weeks
|
Upper extremity reaction test: It is planned to use a validated BlazePod sensor for upper extremity reaction time test
|
4weeks
|
|
Auditory Reaction Test
Time Frame: 4weeks
|
Auditory reaction time will be assessed with the playback.fm
(https://playback.fm/audio-reaksiyon-time)
test.
Subjects will be asked to press the 'space bar' key each time they hear a sound.
After five applications, data will be taken from the output page and the average reaction time will be calculated.
|
4weeks
|
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Bandırma Onyedi EylulU
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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