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Comparison of Traditional and Artificial Intelligence-Assisted Yoga

NCT06186635 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-01-02

No results posted yet for this study

Summary

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:

1. What is the level of quality of life of students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences?
2. What is the level of mental well-being of students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences?
3. Does the traditional yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect the quality of life?
4. 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?
5. Does the traditional yoga program applied to students studying at Çanakkale Onsekiz Mart University, Faculty of Health Sciences affect mental well-being?
6. 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.

Conditions

  • Healthy People

Interventions

OTHER

Traditional yoga

This group will practice traditional yoga for an average of 2 hours, preferably once a week, for 12 weeks.

OTHER

AI-Assisted Yoga

This group will practice AI-assisted yoga for an average of 2 hours, preferably once a week, for 12 weeks.

Sponsors & Collaborators

  • Gözde Özsezer

    lead OTHER

Principal Investigators

  • Gözde Özsezer · Çanakkale Onsekiz Mart University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-01
Primary Completion
2025-08-30
Completion
2025-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06186635 on ClinicalTrials.gov