The Impacts of Mindfulness on Psychological Wellbeing Among Nursing Students (NCT06361394) | Clinical Trial Compass
RecruitingNot Applicable
The Impacts of Mindfulness on Psychological Wellbeing Among Nursing Students
Taiwan240 participantsStarted 2025-02-10
Plain-language summary
The aims of this study are to develop a mindfulness-based elective course for nursing students and to evaluate its effects on psychological well-being, including mindfulness, depression, anxiety, stress, and problematic internet use, empathy, among nursing students.
Who can participate
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Nursing students enrolled at the participating university
* Aged 18 years or older
* Willing to participate in the study
* Able to provide written informed consent
* Enrolled in the elective course "Mindfulness and Happiness" for assignment to the experimental group, or not enrolled in the course for assignment to the comparison group
Exclusion Criteria:
* Younger than 18 years
* Unwilling or unable to provide informed consent
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Perceived Stress Scale score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
2
Generalized Anxiety Disorder 7-Item Scale score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
3
Mindful Attention Awareness Scale score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
4
Chinese version of the Jefferson Scale of Empathy score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
5
The Problematic Internet Use Questionnaire-Short Form (PIUQ-SF) score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
6
Taiwan Five Facet Mindfulness Questionnaire score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
7
Depression, Anxiety, and Stress Scale-21 Score
Timeframe: Baseline (T0) and end of course (T1, 18 weeks)
Trial details
NCT IDNCT06361394
SponsorChang Gung University of Science and Technology