The Effects of Stress Inoculation Training Program on Occupational Stress Level, Coping Style, an… (NCT07105774) | Clinical Trial Compass
CompletedNot Applicable
The Effects of Stress Inoculation Training Program on Occupational Stress Level, Coping Style, and Sleep Quality in New Psychiatric Nurses.
China72 participantsStarted 2024-09-07
Plain-language summary
The aim of this clinical trial is to find out whether a stress inoculation program can reduce occupational stress in new psychiatric nurses. The main question it aimed to answer was:
Does a stress inoculation training program improve participants' occupational stress, coping styles, and sleep quality? The researchers compared the stress inoculation training to a conventional training control to see if the stress inoculation training reduced occupational stress.
Who can participate
Age range
18 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:
* obtained nurse practitioner's license;
* nurses who were newly employed within the last three years and have been in their position for one month or longer;
* directly interacting with patients with mental illnesses in daily work;
* obtained informed consent to participate voluntarily in this study.
Exclusion Criteria:
* non-fresh graduates;
* these taking vacations, refresher courses during the study period;
* were breastfeeding or pregnant;
* had attended a similar stress intervention training (e.g., Positive Thinking Stress Reduction training, etc.) within the past year;
* new major non-work stressors (e.g., death of a close family member, divorce, exposure to a major natural disaster, etc.) within the last six months.
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
Job stress scale for newly-graduated nurses (JSSNGN)
Timeframe: From enrollment to the end of treatment at 12 weeks