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临床试验/NCT06491797
NCT06491797尚未招募不适用

Booster of the "More Time for Patients" Program: a Cluster Randomized Controlled Trial

University Hospital, Geneva1 个研究点 分布在 1 个国家目标入组 764 人开始时间: 2024年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
764
试验地点
1
主要终点
Timely delivery of appropriate analgesic

研究概览

简要总结

The goal of this clinical trial is to determine if reactivating a hospital program called "Plus de temps au service des patients" (PTP) can improve the quality of pain management for patients and increase job satisfaction among healthcare professionals. The main questions this study aims to answer are:

  • Does reactivating PTP improve the quality of pain management?
  • Does reactivating PTP increase healthcare professionals' job satisfaction? In this study, researchers will compare the effects of reactivating the program immediately to reactivating it after a 3-month delay.

Participants in the trial are healthcare professionals who will:

  • Select 2 or 3 elements of the program they believe would be most beneficial to reactivate in their hospital units.
  • Implement the selected elements for 3 months.
  • Complete job satisfaction and burnout questionnaires before and after the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •for the units:
  • •Implementation of PTP finished at least 6 months previously
  • •Agreement to the study from both medical head of service and head of unit (IRES)
  • •Inclusion criteria for healthcare professionals:
  • •Healthcare professionals >18 yo.
  • •Healthcare professionals working in a HUG service of medicine or surgery.
  • •Healthcare professionals include Physicians, Nurses, Assistant Nurses, Pharmacists, Physiotherapists and other physical therapists.
  • •Provided general informed consent.
  • •Inclusion criteria for patients
  • •Patients hospitalised in one of the boosted units.
  • •Cognitive ability to provide satisfaction assessment.

排除标准

  • 未提供

研究组 & 干预措施

Immediate reactivation

Experimental

Our intervention will be booster measure of the existing PTP elements that will be designed for each unit that has been randomized to the immediate intervention group. The booster will consist in a reactivation through audit and feedback of 2-3 elements of the PTP program. The selection of the elements to boost will be done locally in each unit through a coordinated discussion between representants of the PTP organization and representants of the unit's medical and nursing professionals. This will create an adaptable intervention that will feature selected standards among the list of 36 existing standards. The boost will be performed over 3 months

干预措施: Immediate reactivation (Behavioral)

Delayed reactivation

No Intervention

The control intervention will also be PTP as applied usually, in the control group before the application of the booster measure (applied delayed by three months).

结局指标

主要结局

Timely delivery of appropriate analgesic

时间窗: Timely is operationalized as maximum 6 hours before for reserve pain medication, and up to 1 hour after pain measurement for any medication appropriate to the level of pain.

Quality of pain management as recorded through the timely delivery of an appropriate level painkiller after any pain Visual Analog Scale (VAS) ≥4. VAS score range from 0 to 10, 0 being no pain and 10 being the worse pain imaginable.

次要结局

  • Pain VAS documentation(12 hours)
  • Healthcare professionals' burnout(Once before the reactivation and once after (month 1 and month 3))
  • Healthcare professional's absenteeism rate(At month 1, 2 and 3 corresponding to the period of study)
  • Healthcare professionals' satisfaction(Once before the reactivation and once after (month 1 and month 3))
  • Healthcare professionals' risk of turnover(Once before the reactivation and once after (month 1 and month 3))
  • Patient satisfaction - daily(Every day from month 1 to month 3 corresponding to the period of study)
  • Patient satisfaction - Picker(1 week after discharge for every patients.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Agoritsas

Professor

University Hospital, Geneva

研究点 (1)

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