Improving the Quality of End-of-Life Communication for Patients With COPD

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00106080
First received: March 18, 2005
Last updated: August 1, 2012
Last verified: May 2008

March 18, 2005
August 1, 2012
November 2004
May 2008   (final data collection date for primary outcome measure)
Quality of Patient Clinician Communication About End-of-Life Care(QOC) score [ Time Frame: Measured at enrollment and post-intervention ] [ Designated as safety issue: No ]
Quality of Patient Clinican Communication About End-of-Life Care (QOC) score
Complete list of historical versions of study NCT00106080 on ClinicalTrials.gov Archive Site
Effect of the intervention on self-reported end-of-life discussions between patient, reported independently by patient and provider, and patient and surrogate. Assess baseline desire for and the quality of end-of-life communication. [ Time Frame: Measured at enrollment and post-intervention ] [ Designated as safety issue: No ]
Effect of the intervention on self-reported end-of-life discussions between patient, reported independently by patient and provider, and patient and surrogate. Assess baseline desire for and the quality of end-of-life communication, facilitators.
 
 
 
Improving the Quality of End-of-Life Communication for Patients With COPD
Improving the Quality of End-of-Life Communication for Patients With COPD

The purpose of this study is to evaluate a multifaceted intervention to improve the quality of end-of-life communication between patients with COPD and their primary care providers using information about patients preferences for end of life care and how to communicate and use this information to activate patients, family members, and healthcare providers.

This project builds on previous work that described preferences important to patients at end-of-life and desire for life-sustaining therapy by incorporating these attributes into a multifaceted intervention designed to improve the quality of end-of-life communication.

Our specific aim is to evaluate a multifaceted intervention to improve the quality of end-of-life communication between patients with moderate or severe COPD and their primary care providers. The intervention is based on self-efficacy theory and includes provider education, local champions and role models, determination of patients individual barriers and facilitators regarding communication about end-of-life care, preferences for communication about end-of-life care and preferences for end-of-life care and using this information to activate patients, family members, and healthcare providers.

If successful, the methods used for this study could be translated into clinic practice and possibly generalized to other chronic life-threatening conditions

Interventional
 
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Investigator)
  • Pulmonary Disease
  • Palliative Care
Behavioral: Audit and Feedback
Individualized summaries of patient's preferences regarding communication about end-of-life care and preferences for end-of-life care to activate patients, family members, and healthcare providers.
  • Experimental: Arm 1
    Provider and surrogate summaries of patient's preferences for health care communication and treatment.
    Intervention: Behavioral: Audit and Feedback
  • No Intervention: Arm 2
    Usual care

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
400
May 2008
May 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

One or more of the following:

1 Have 3 or more outpatient clinics visits for COPD (ICD-9) in the two years prior to enrollment.

2. Have been hospitalized with a primary discharge diagnosis (ICD-9) for COPD in the two years prior to enrollment.

3. Active use of inhaled beta-agonist and ipratropium bromide (or equivalent in combination inhalers like Combivent) in the 12 months prior to enrollment.

Plus

  1. Have a future visit scheduled in one of the eligible primary care or chest clinics; and
  2. Have airflow limitation

Exclusion Criteria:

  1. If they have cognitive dysfunction, language barriers or severe psychiatric disorder that would preclude them from completing the questionnaires. This will be assessed initially by the patients provider and by the research assistant during in-person interviews.
  2. The provider taking care of their COPD does not participate.
  3. Have a new diagnosis of COPD within the last month.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00106080
IIR 02-292
No
Department of Veterans Affairs
Department of Veterans Affairs
 
Principal Investigator: David H. Au, MD MS VA Puget Sound Health Care System, Seattle
Department of Veterans Affairs
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP