- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06186635
Comparison of Traditional and Artificial Intelligence-Assisted Yoga
Comparison of the Effects of Traditional and Artificial Intelligence-Assisted Yoga on Quality of Life and Mental Well-Being: A Randomized Controlled Study
The goal of the study was to compare the effects of traditional yoga and AI-assisted yoga practice on quality of life and mental well-being in students in a randomized controlled trial. The main question[s] it aims to answer are:
- What is the level of quality of life of students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences?
- What is the level of mental well-being of students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences?
- Does the traditional yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect the quality of life?
- Does the artificial intelligence-supported yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect the quality of life?
- Does the traditional yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect mental well-being?
- Does the artificial intelligence-supported yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect mental well-being?
Participants will take part in a traditional and AI-assisted yoga practice. The researchers will compare the effect of traditional yoga and AI-assisted yoga on quality of life and mental well-being.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Gözde Özsezer
- Phone Number: +905077548552
- Email: gozdeozsezer@hotmail.com
Study Contact Backup
- Name: Gülengül Mermer
- Phone Number: +905054515631
- Email: gulengul.s.mermer@ege.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a student at Çanakkale Onsekiz Mart University, Faculty of Health Sciences, Department of Nursing, Midwifery, Emergency Aid and Disaster Management.
- Volunteering to participate in the study
- Not having any physical dysfunction that would prevent yoga (COPD, septum deviation, etc.)
- Not having chronic diseases that would prevent yoga (Breast CA, epilepsy, chemotherapy, radiotherapy, stage 3 hypertension >180/110)
- Not having done yoga before
- Being open to communication
- Having internet access.
- Having a computer/tablet/phone with a camera.
Exclusion Criteria:
- Having a physical or mental health problem that will prevent and/or limit practicing yoga.
- Having had a surgical operation within the last month
- Having had a cancer-related surgical operation within the last year
- Not volunteering to participate in the study
- Not wanting to turn on his camera.
- Doing yoga regularly
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Traditional yoga group
This group will practice traditional yoga for an average of 2 hours, preferably once a week, for 12 weeks.
|
This group will practice traditional yoga for an average of 2 hours, preferably once a week, for 12 weeks.
|
|
Experimental: AI-Assisted Yoga
This group will practice AI-assisted yoga for an average of 2 hours, preferably once a week, for 12 weeks.
|
This group will practice AI-assisted yoga for an average of 2 hours, preferably once a week, for 12 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Multidimensional Quality of Life Scale
Time Frame: 6 months after interventions
|
1.
The Multidimensional Quality of Life Scale total score varies between 35-245.
Higher scores represent better functional status.
|
6 months after interventions
|
|
Waarwick-Edinburg Mental Well-Being Scale
Time Frame: 6 months after interventions
|
2. A minimum of 14 and a maximum of 70 points are obtained from the Waarwick-Edinburg Mental Well-Being Scale.
High scores from the scale indicate high mental (psychological) well-being.
|
6 months after interventions
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gözde Özsezer, Çanakkale Onsekiz Mart University
Publications and helpful links
General Publications
- undefined
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 2023-YÖNP-0911
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
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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