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Generative Artificial Intelligence Nurse Staffing Study

No phase Interventional Burnout, Healthcare Workers

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Generative Artificial Intelligence Nurse Staffing (GAINS) Intervention.
Who it may be relevant to
Registry conditions: Burnout, Healthcare Workers. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Generative Artificial Intelligence Nurse Staffing (GAINS) Study

Overview

This study is guided by Maslach's Burnout Theory and with Normalization Process Theory supporting the implementation of the GAINS intervention by facilitating its integration into routine system-level practice. In Year 1, the investigative team will collaborate with hospital-based nursing leadership and key stakeholders to identify staffing-specific factors essential for operationalizing the GAINS AI model/intervention. In Year 1, the investigators will also conduct a survey amongst nursing staff to measure baseline burnout. In Year 2, the AI-staffing intervention will be implemented with the medical-surgical nursing float pool team. In Year 3, the investigators will first repeat the nurse burnout survey and second, expand the intervention to include the nursing assistant float pool team. In Year 4, the investigators will conduct the final burnout survey with nurses, assess feasibility of GAINS (target vs. actual staffing- nurses and nursing assistants), and assess preliminary efficacy of GAINS to reduce costs related to staffing. the investigators will compare outcomes at three time points (pre, mid, and post-intervention). Interviews with nurses, nursing assistants, unit nurse managers, and leadership will further explicate the intervention's acceptability, feasibility, and impact on burnout.

Interventions

  • Other Generative Artificial Intelligence Nurse Staffing (GAINS) Intervention
    The Generative Artificial Intelligence intervention is an industrial engineering and nursing-informed innovation developed to optimize team-based staffing of registered nurses and nursing assistants. We anticipate that the GAINS intervention will enhance staffing efficiency, reduces reliance on travel nurses, minimizes overtime costs, and supports nurse well-being by proactively managing workload distribution and reducing burnout. At the core of GAINS is a generative AI model that predicts futur

Primary outcome measures

  • Maslach's Burnout Inventory [Time frame: Up to 2.5 years]
  • Qualitative Interviews to Evaluate Feasibility, Normalization, and Acceptability of the GAINS Intervention [Time frame: Up to 3 years]
Secondary outcome measures (2)
  • Optimization Staffing Rates [Target staffing rate - Actual staffing rate] [Time frame: Up to 2 years]
  • Total Cost: Travel Nurse and Nurse Overtime [Time frame: Up to 2 years]

Eligibility criteria

Inclusion criteria

  • Registered nurses, nursing assistants, or key stakeholders
  • Employed by The Queen's Medical Center
  • Working at least 24 hours per week
  • Position associated with medical-surgical units where float pool nurses work

Exclusion criteria

  • Employees working less than 24 hours per week at The Queen's Medical Center
  • Employees whose roles are not related to medical-surgical units

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Sequential
Masking
Open label
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06978790 · 41775

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗