- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07497022
Effectiveness of Mindful Attention Awareness Breathing on Attention and Wellbeing Among Undergraduate Students (MAAB)
Enhancing Attention and Well-Being Through Mindful Attention Awareness Breathing: An Interventional Study Among Undergraduates
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Nursing students must develop self-awareness and emotional stability to effectively interact with patients who come from diverse backgrounds and present with varied healthcare needs. During undergraduate education, students face the dual demands of theoretical learning and clinical practice, which can affect their attention, awareness, and overall well-being. Mindfulness-based practices, particularly breathing techniques, have been shown to support cognitive functioning and emotional balance. Mindful Attention Awareness Breathing is a structured breathing-based mindfulness practice that encourages individuals to focus on their breathing and remain aware of the present moment without judgment.
This experimental study was conducted among undergraduate nursing students in a selected teaching institution to evaluate the effectiveness of Mindful Attention Awareness Breathing on attention, mindfulness, and subjective well-being. Students in the intervention group participated in guided breathing sessions conducted daily for a specified period, while the control group continued with routine academic activities. Attention, mindfulness, and awareness were assessed using standardized instruments, and subjective well-being was measured using a validated student well-being questionnaire.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Tamil Nadu
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Chennai, Tamil Nadu, India, 600116
- Sri Ramachandra Institute of Higher Education and Research
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students who are willing and available for 15 days. Students from the first and second year of B.Sc. Nursing
Exclusion Criteria:
- Students who are not willing to undergo the mindful breathing practice. Students having chronic respiratory conditions and poor attention span
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Mindful Breathing Group
45 first-year students, and 40 second year students were allocated to study group.
These students received supervised practice of mindful breathing techniques for 15 days.Intervention sessions were held every day for 20 minutes over 15 consecutive days in morning for the first year B.Sc. Nursing students and afternoon for the second year students.
Students were divided into small groups of 10-12 for close observation and asked to assemble in the classroom.
The exercises practiced in each session followed a structured sequence which includes pursed-lip breathing for 5 minutes, followed by box breathing for 3-4 minutes and 4-7-8 breathing for 5 minutes, diaphragmatic breathing for 4 minutes, and alternate nostril breathing for about 5 minutes.
Students maintained proper posture, eye closure, and breath awareness throughout, with short relaxation intervals between exercises, and concluded with relaxation by placing the palms over the eyes.
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The exercises practiced in each session followed a structured sequence which includes pursed-lip breathing for 5 minutes, followed by box breathing for 3-4 minutes and 4-7-8 breathing for 5 minutes, diaphragmatic breathing for 4 minutes, and alternate nostril breathing for about 5 minutes.
Students maintained proper posture, eye closure, and breath awareness throughout, with short relaxation intervals between exercises, and concluded with relaxation by placing the palms over the eyes.
Other Names:
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No Intervention: Control group
45 first-year and 40 second year students were allocated to control group and they did not receive the intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mindfulness
Time Frame: The assessment was done at baseline on day one and posttest on 15th day of the intervention
|
Mindful Attention Awareness Scale A 15-item self-report scale measuring attention and awareness.
Total score ranges from 15 to 90, with higher scores indicating greater mindfulness.
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The assessment was done at baseline on day one and posttest on 15th day of the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attention
Time Frame: Baseline was assessed on day 1 before starting the intervention and posttest was obtained on 15th day of the intervention
|
Attention was determined using the Digit Span Test with total score ranging from 0 to 30, with higher scores indicating better cognitive performance.
|
Baseline was assessed on day 1 before starting the intervention and posttest was obtained on 15th day of the intervention
|
|
Well Being
Time Frame: Baseline on Day 1 and post-intervention Day 15
|
The wellbeing of the students was assessed using the Student Subjective Well-being Questionnaire a 16-item questionnaire with total scores range from 1-64 and higher scores indicating greater wellbeing The effectiveness of the intervention is determined on all the three components and a correlation is done to determine their effects on each other
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Baseline on Day 1 and post-intervention Day 15
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Collaborators and Investigators
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
Keywords
Other Study ID Numbers
- 146/141
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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