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Evaluation of Methods for Implementation of a Comfort Care Order Set

Not Applicable
Completed
Conditions
Terminal Conditions, End of Life
Interventions
Other: Basic Implementation Approach
Other: Enhanced Implementation Approach
Registration Number
NCT02383173
Lead Sponsor
VA Office of Research and Development
Brief Summary

The overarching goal of this research program is to improve the quality of end-of-life care provided to Veterans dying in VA Medical Centers (VAMCs), by transferring the best practices of home hospice and palliative care for the last days and hours of life into the inpatient setting. This trial will examine two methods of delivering a Comfort Care Education Intervention utilizing the established infrastructure of VA Palliative Care Consult Teams (PCCT): a Basic Implementation Approach using a teleconference to review educational materials and activate PCCTs to educate other providers, and an Enhanced Implementation Approach utilizing in-person, train-the-"champion" workshops to prepare PCCT members to be leaders and trainers at their home sites. Findings will provide a robust evaluation of the implementation process, and will be used to refine the Comfort Care Education Intervention and implementation strategies in preparation for nationwide dissemination of best practices for end-of-life care within the VA Healthcare System.

Detailed Description

Anticipated Impacts on Veterans' Healthcare: The overarching goal of this research program is to improve the quality of end-of-life care provided to Veterans dying in VA Medical Centers (VAMCs), by transferring the best practices of home hospice and palliative care for the last days and hours of life into the inpatient setting.

Project Background: Often, patients who are near the end of life are not recognized as actively dying. As a result, their suffering may not be appreciated or managed properly, and may even be exacerbated by usual medical care when aggressive, futile, or iatrogenically harmful treatments are continued. During this time, supportive and comfort care treatment plans can be implemented to reduce suffering and improve the quality of care provided to these patients. The investigative team has developed and evaluated an education-based intervention to teach providers how to identify patients who are actively dying and to implement care plans appropriate for the last days or hours of life. To facilitate use of these interventions, an electronic Comfort Care Order Set (CCOS) was designed and integrated into the Computerized Patient Record System (CPRS) to support and guide the selection of comfort care treatments. The effectiveness of the Comfort Care Education Intervention has been demonstrated in 7 VAMCs and it is ready for implementation on a broader scale.

Project Objectives: This trial will extend this line of research by examining two methods of delivering this Comfort Care Education Intervention utilizing the established infrastructure of Palliative Care Consult Teams (PCCT): a Basic Implementation Approach using a teleconference to review educational materials and activate PCCTs to educate other providers, and an Enhanced Implementation Approach utilizing in-person, train-the-"champion" workshops to prepare PCCT members to be leaders and trainers at their home sites. The aims of this study are 1) to compare the effectiveness of the two approaches for changing provider behavior, as reflected in documented processes of end-of-life care, 2) to formatively evaluate PCCT members' experiences with and perceptions of the two approaches, and 3) to quantitatively evaluate PCCT members' perceptions of the training received and its impact on attitudes, skills, and perceived efficacy to care for patients and teach other providers.

Project Methods: PCCTs at 47 VA Medical Centers will be recruited to participate in the trial and randomized to receive the Comfort Care Education Intervention using the Basic or the Enhanced Implementation Approach. Data on processes of end-of-life care will be abstracted from the CPRS medical records of Veterans who die before and after the interventions, including presence of an active opioid order at time of death (primary endpoint), other medication orders and administration, do-not-resuscitate orders, palliative care consult orders, location of death, presence of nasogastric tubes/intravenous lines, restraints, and pastoral care. Semi-structured telephone interviews will be conducted with all participating PCCT members to explore their perceptions of training, the process of teaching other providers at each site, barriers and facilitators they encountered, how prepared they felt to overcome these barriers, and specific needs and preferences regarding the implementation approach.

Findings will provide a robust evaluation of the implementation process, and will be used to refine the Comfort Care Education Intervention and implementation strategies in preparation for nationwide dissemination of best practices for end-of-life care within the VA Healthcare System.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
134
Inclusion Criteria

To be eligible, each provider had to be a member of a VA palliative care consult team (PCCT)

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Exclusion Criteria

VAMCs were excluded if the facility scored in the top 10th percentile or lowest 10th percentile on PROMISE after-death survey; if they had no prescribing provider on the PCCT team; or if there were fewer than 30 deaths in VAMC during the reporting period

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Basic Implementation ApproachBasic Implementation ApproachBasic approach to implementing a Comfort Care Education Intervention utilizing the established infrastructure of Palliative Care Consult Teams
Enhanced Implementation ApproachEnhanced Implementation ApproachEnhanced approach to implementing a Comfort Care Education Intervention utilizing the established infrastructure of Palliative Care Consult Teams
Primary Outcome Measures
NameTimeMethod
Presence of an Active Opioid Order at Time of Deathat time of death for veterans who died in the 9 months following the intervention period

presence of an active opioid order at time of death in Veteran's medical record

Secondary Outcome Measures
NameTimeMethod
Presence of a Palliative Care Consult Orderlast 7 days of life for veterans who died in the 9 months following the intervention period

presence of a palliative care consult order in the last 7 days of life

Presence of a Do-not-resuscitate Orderlast 7 days of life for veterans who died in the 9 months following the intervention period

presence of a do-not-resuscitate order in the last 7 days of life

Presence of an Intravenous Linein the 9 months following the intervention period

presence of an intravenous line at time of death

Presence of a Pastoral Care Visitlast 7 days of life for veterans who died in the 9 months following the intervention period

presence of a pastoral care visit in the last 7 days of life

Presence of an Order for Benzodiazepine Medicationlast 7 days of life for veterans who died in the 9 months following the intervention period

presence of an order for benzodiazepine medication in the last 7 days of life

Location of Deathin the 9 months following the intervention period

death in intensive care unit

Presence of a Nasogastric Tubein the 9 months following the intervention period

presence of a nasogastric tube at time of death

Presence of Restraintsin the 9 months following the intervention period

presence of restraints at time of death

Trial Locations

Locations (1)

Birmingham VA Medical Center, Birmingham, AL

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Birmingham, Alabama, United States

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