Skip to content

Yoga, Meditation and Mindful Eating Intervention in University Students

Evaluation of a Yoga, Meditation and Mindful Eating Intervention for the Control of Stress, Anxiety, Depression, and Mindfulness in University Students

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07280078
Acronym
Yoga-UDEA
Enrollment
60
Registered
2025-12-12
Start date
2026-07-01
Completion date
2026-08-01
Last updated
2026-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Mindfulness, Stress, Psychological, Well-being

Keywords

Yoga, Meditation, Stress, Psychological; Anxiety; Well-being; Mindful Eating; Psychological

Brief summary

The aim of this study is to learn whether a program that combines yoga, meditation, and mindful eating can help reduce stress, anxiety, and depression, and improve mindfulness in university students. The main questions the study aims to answer are: * Does participating in yoga, meditation, and mindful eating sessions lower students' levels of stress, anxiety, and depression? * Does the program improve students' mindfulness and general well-being? What will happen in the study: Participants will: * Attend weekly sessions of yoga, meditation, and mindful eating for 32 hours total. * Practice physical postures (Asanas), breathing exercises (Pranayama), relaxation, and meditation. * Receive short lessons about mindful nutrition and healthy lifestyle habits. * Complete questionnaires before and after the program to measure stress, anxiety, depression, and mindfulness.

Interventions

BEHAVIORALYoga, Meditation, and Mindful Eating

The behavioral intervention combines weekly 2-hour sessions for 16-weeks. Each class includes warm-up exercises, yoga postures for balance and flexibility, breathing techniques (pranayamas), guided meditation, and relaxation. Additionally, participants receive recommendations on healthy habits, conscious nutrition, and physical well-being.

Sponsors

Universidad de Antioquia
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Undergraduate students enrolled in the curso "Yoga, Meditation, and Mindful Eating" at the Faculty of Pharmaceutical and Food Sciences (CIFAL), University of Antioquia. * Willing to participate voluntarily and complete all study assessments. * Able to attend the full program (32 hours over one academic semester).

Exclusion criteria

* Students currently practicing yoga or meditation regularly. * Pregnant women or participants with any medical condition that prevents safe participation in yoga practice. * Individuals with severe psychiatric disorders requiring pharmacological treatment.

Design outcomes

Primary

MeasureTime frameDescription
Change in academic stress levels measured by the Academic Stress ScaleBaseline (Week 1, pre-test) and Week 16 (post-intervention).Academic stress will be assessed using the Academic Stress Scale, a 54-item self-report questionnaire that evaluates methodological, social, and emotional stressors related to academic activities. Each item is scored on a Likert-type scale. Total scores range from 54 to 270, with higher scores indicating higher levels of perceived academic stress.

Secondary

MeasureTime frameDescription
Change in anxiety levels measured by the State-Trait Anxiety Inventory (STAI)Baseline (Week 1, pre-test) and Week 16 (post-intervention).Anxiety will be assessed using the State-Trait Anxiety Inventory (STAI), a 40-item self-report instrument consisting of two subscales: State Anxiety (20 items) and Trait Anxiety (20 items). Each subscale score ranges from 20 to 80, with higher scores indicating greater anxiety levels.
Change in depressive symptoms measured by the Beck Depression Inventory-II (BDI-II)Baseline (Week 1, pre-test) and Week 16 (post-intervention).Depressive symptoms will be assessed using the Beck Depression Inventory-II (BDI-II), a 21-item self-report questionnaire. Each item is scored from 0 to 3. Total scores range from 0 to 63, with higher scores indicating more severe depressive symptoms.

Contacts

CONTACTJavier M Ceballos Rrueda, PhD
javier.ceballos@udea.edu.co+57 3174268448

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026