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Completed

NCT Number: NCT00234286

Intervention to Improve Care at Life's End

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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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Birmingham VA Medical Center

Birmingham, Alabama, 35233, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aim 1: Not applicable. Patients were deceased.
  • Aim 2: After-death interviews with next of kin: must be willing and able to participate in after-death interview at local VA Medical Center.

Exclusion criteria

  • N/A

Treatment and study plan

Comfort care education intervention

Behavioral

Comfort care education intervention, consisting of intensive, on-site staff training together with an electronic order set for palliative care and educational materials

Primary outcomes

  1. Presence of Order for Opioid Pain Medication

    Time frame: Pre and Post Intervention

    Presence of order for opioid pain medication at time of death based on abstraction of electronic medical record

Secondary outcomes

  1. Do Not Resuscitate Order

    Time frame: Pre and Post Intervention

    Presence of a Do Not Resuscitate order at time of death based on abstraction of electronic medical record

  2. Number of Patients Who Died in ICU

    Time frame: Pre and Post Intervention

    Location of death (ICU vs. other) based on abstraction of electronic medical record

  3. Individuals With a Nasogastric Tube

    Time frame: Pre and Post Intervention

    Presence of nasogastric tube based on abstraction of electronic medical record

  4. Individuals With an Intravenous Line

    Time frame: Pre and Post Intervention

    Presence of intravenous line infusing at time of death based on abstraction of electronic medical record

  5. Number of Individuals Who Died in Restraints

    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

  6. Individuals Administered of Opioid Medication

    Time frame: Pre and Post Intervention

    Administration of opioid medication based on abstraction of medical record

  7. Individuals With an Order for Antipsychotic Medication

    Time frame: Pre and Post Intervention

    Order for antipsychotic medication based on abstraction of medical record

  8. Individuals Administered Antipsychotic Medication

    Time frame: Pre and Post Intervention

    Administration of antipsychotic medication based on abstraction of medical record

  9. Individuals With an Order for Benzodiazepine Medication

    Time frame: Pre and Post Intervention

    Order for benzodiazepine medication based on abstraction of medical record

  10. Individuals Who Received Benzodiazepine Medication

    Time frame: Pre and Post Intervention

    Administration of benzodiazepine medication based on abstraction of medical record

  11. Individuals Who Received Scopolamine

    Time frame: Pre and Post Intervention

    Administration of scopolamine (for death rattle) based on abstraction of medical record

  12. Sublingual Administration

    Time frame: Pre and Post Intervention

    Sublingual administration of medication based on abstraction of medical record

  13. Individuals With Pastoral Care Visit

    Time frame: Pre and Post Intervention

    Pastoral Care Visit based on abstraction of medical record

  14. Individuals With an Advance Directive

    Time frame: Pre and Post Intervention

    Presence of advance directive based on abstraction of medical record

  15. Individuals With a Palliative Care Consultation

    Time frame: Pre and Post Intervention

    Palliative Care Consultation based on abstraction of medical record

Sponsors and collaborators

Lead sponsor

US Department of Veterans Affairs

Fed

Registry information

Official study title

Intervention to Improve Care at Life's End in VA Medical Centers

Acronym: BEACON

Important dates

Study start
2005
Primary completion
2011
Study completion
2013
First posted
Oct 6, 2005
Registry last updated
Apr 27, 2015

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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