Birmingham VA Medical Center
Birmingham, Alabama, 35233, United States
NCT Number: NCT00234286
The BEACON trial (Best Practices for End-of-Life Care for Our Nations' Veterans) was a six-site implementation study to evaluate a multi-component, education-based intervention to improve the quality of end-of-life care provided in VA Medical Centers.
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Interventional
Not applicable
Birmingham, Alabama, 35233, United States
The BEACON trial (Best Practices for End-of-Life Care for Our Nations' Veterans) was a six-site, real-world implementation trial of a multi-component, education-based intervention to improve the quality of end-of-life care conducted in VA Medical Centers (VAMCs).
The primary aim was to evaluate the effectiveness of a multi-component intervention for improving processes of care provided in the last days of life in VAMCs. The second aim was to conduct after-death interviews with next-of-kin and qualitative analysis of their perceptions of the care provided to the veteran and family.
The multi-component intervention targeted VAMC inpatient providers, including physician, nursing, and ancillary staff. It consisted of preparatory site visits, a staff training program, a newly developed Comfort Care order set decision support tool built into the CPRS, and follow-up consultation. The intervention team travelled to each site to conduct two weeks of comprehensive in-service training. Staff were trained to identify actively-dying patients and implement a set of best practices of traditionally home-based hospice care for dying patients. The team provided assistance with policies, procedures, and skill training needed to implement comfort care interventions. Introduction of the intervention at each VAMC was staggered across time at six-month intervals using a multiple-baseline, stepped wedge design.
Data on processes of end-of-life care (last 7 days) were abstracted from the CPRS medical records of all veterans who died before, during, and after the intervention (January 2005-February 2011). A priori, five processes of care were identified as primary endpoints to indicate quality of end-of-life care: 1) presence of an order for opioid pain medication at time of death; 2) a do-not-resuscitate (DNR) order in place at time of death; 3) location of death; 4) presence of enteral feeding tube or intravenous line at time of death; and 5) physical restraints in place at or near time of death.
In addition, in-depth, face-to-face interviews were conducted with 78 bereaved next-of-kin.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Comfort care education intervention, consisting of intensive, on-site staff training together with an electronic order set for palliative care and educational materials
Time frame: Pre and Post Intervention
Presence of order for opioid pain medication at time of death based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Presence of a Do Not Resuscitate order at time of death based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Location of death (ICU vs. other) based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Presence of nasogastric tube based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Presence of intravenous line infusing at time of death based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Presence of restraints at or near time of death at time of death based on abstraction of electronic medical record
Time frame: Pre and Post Intervention
Administration of opioid medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Order for antipsychotic medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Administration of antipsychotic medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Order for benzodiazepine medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Administration of benzodiazepine medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Administration of scopolamine (for death rattle) based on abstraction of medical record
Time frame: Pre and Post Intervention
Sublingual administration of medication based on abstraction of medical record
Time frame: Pre and Post Intervention
Pastoral Care Visit based on abstraction of medical record
Time frame: Pre and Post Intervention
Presence of advance directive based on abstraction of medical record
Time frame: Pre and Post Intervention
Palliative Care Consultation based on abstraction of medical record
US Department of Veterans Affairs
Fed
Intervention to Improve Care at Life's End in VA Medical Centers
Acronym: BEACON
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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