- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07631117
Yoga Nidra for Stress, Sleep Quality, and Academic Resilience in Nursing Students (YNSAR)
Effects of Nidra Yoga Intervention on Psychological Stress, Sleep Quality, and Academic Resilience Among Nursing Students During Clinical Practicum
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 1120201
- MacKay Junior College of Medicine, Nursing, and Management
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 1.1 Fifth-year nursing students from a junior college of medicine, nursing, and management who will participate in clinical practicum courses from February 2026 to December 2026 across six classes. Students from classes taught by the principal investigator will not be included.
1.2 Students without any major family or personal life events during the study period, as confirmed during verbal recruitment by the principal investigator.
1.3 Students who agree to complete the questionnaires and participate in the study.
1.4 Students who have not participated in any form of yoga or meditation practice.
Exclusion Criteria:
- 2.1 Students experiencing major family or personal life events at the time of verbal recruitment.
2.2 Students who have participated in any form of yoga or meditation practice. 2.3 Students from classes taught by the principal investigator.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Yoga Nidra Intervention Group
Participants in this group will receive a structured Yoga Nidra intervention during the clinical practicum period.
The intervention will be delivered through guided online audio sessions conducted four times per week for 16 consecutive weeks, with each session lasting approximately 30 minutes.
Participants will subsequently continue home-based Yoga Nidra practice during the clinical practicum period.
|
Participants in this group will receive a structured Yoga Nidra intervention during the clinical practicum period.
The intervention will be delivered through guided online audio sessions conducted four times per week for 16 consecutive weeks, with each session lasting approximately 30 minutes.
Participants will subsequently continue home-based Yoga Nidra practice during the clinical practicum period.
|
|
No Intervention: Control Group
Participants in this group will receive routine educational support and regular clinical practicum training during the study period without participation in the Yoga Nidra intervention program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical Practicum Stress
Time Frame: Baseline, 3 months after the intervention, and 6 months after the intervention
|
Changes in nursing students' clinical practicum stress measured using the Nursing Students' Clinical Practicum Stress Scale.
|
Baseline, 3 months after the intervention, and 6 months after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anxiety
Time Frame: Baseline, 3 months, and 6 months
|
Changes in anxiety levels measured using the Generalized Anxiety Disorder-7 (GAD-7).
|
Baseline, 3 months, and 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: chin-ting lee, MSN, RN, MacKay Junior College of Medicine, Nursing, and Management
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 26MMHIS034e
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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