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NCT05722249
Interventions to Promote Well-being of Nightshift Nursing Team Members
Conditions: Professional Quality of Life
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 221
Sponsor: Children's National Research Institute
Location: United States
Summary
Background:Nightshift health care employees can experience greater likelihood of health threats such as weight gain, hypertension, and sleep disturbances.
Evidence indicates a willingness of nightshift health care professionals to engage in wellness activities initiated at the work setting and during the assigned nightshift.
In this single site study at a freestanding pediatric tertiary care hospital, inpatient units will be randomized to one of two nightshift interventions during an 8-week study period (mindfulness plus sleep hygiene or physical activity plus sleep hygiene).
Immediately following the first study period, the randomized units will begin a second study period in which they will continue with the intervention first received but shall add the intervention not initially received.
While there are hundreds of studies that describe the adverse health and safety effects of night shift work, there are few studies where interventions are tested for their efficacy to reduce the harm to workers or improve their well-being.
Currently the few intervention studies that exist focus on the scheduling, duration and timing of work shifts, the timing of meals, and aspects of lighting in the workplace.
Other interventions, such as those proposed in this study, have not been tested systematically using a rigorous design.Purpose and Methods:The purpose of this study, using a cluster cross-over randomized trial design, is to measure the impact on professional quality of life (primary endpoint) and medication administration error, role-related meaning, and sleep quality (secondary endpoints) of either a mindfulness intervention plus sleep hygiene (Arm A) or a physical activity intervention plus sleep hygiene (Arm B) in the first study period, and the combination of both interventions on the same outcomes in the second study period for nightshift health care employees.
Eligibility Criteria
Inclusion Criteria:Eligible participants will be nurses and members of the nursing care team that work the nightshift fulltime or that rotate from the dayshift to the nightshift on a routine basis.
Participants will need to be scheduled to work at least 2 weeks of the nightshift during each study period (Study Period 1, Study Period 2) to be fully eligible to participate in the study.
To be fully eligible, participants must be able to complete a consent process and understand the study design and the self-report periods.Exclusion Criteria:Exclusion criteria would include nurses and nursing care team members who do not rotate regularly to the nightshift or who work only the dayshift.
Source: ClinicalTrials.gov (NCT05722249). StuddyBuddy aggregates publicly available trial information.