Adaptation and Evaluation of RESTORE (NCT07104474) | Clinical Trial Compass
By InvitationNot Applicable
Adaptation and Evaluation of RESTORE
United States470 participantsStarted 2025-12-02
Plain-language summary
The purpose of this clinical trial is to test whether the RESTORE intervention works to reduce nurse burnout, by engaging nursing staff in system redesign to reduce job demands and increase job resources.
Participants in the RESTORE intervention process will be interviewed about:
* their experience with RESTORE
* their experiences working on a unit where RESTORE was used
Participants will also complete surveys of the impact of RESTORE on job demands, job resources, burnout, and work engagement.
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.
Aim 1 and Aim 2:
Inclusion Criteria:
* Nursing staff employed on one of the study units and involved in direct patient care
Exclusion Criteria:
* Nursing staff that are not involved in direct patient care, travel and float nursing staff
Aim 3:
Inclusion Criteria:
\- Hospital and system leaders from one of the following groups
* leaders from hospitals that participated in Aims 1 and 2, OR
* other leaders from our partner health systems, OR
* leaders from other hospital settings
* leaders from hospital advocacy or quality organizations
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
Change in Maslach Burnout Inventory (MBI)
Timeframe: Baseline to 30 months (measured quarterly)