Improving the Quality of End-of-Life Communication for Patients With COPD
Tracking Information | |||||
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First Received Date ICMJE | March 18, 2005 | ||||
Last Updated Date | August 1, 2012 | ||||
Start Date ICMJE | November 2004 | ||||
Primary Completion Date | May 2008 (final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures ICMJE |
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 ] | ||||
Original Primary Outcome Measures ICMJE |
Quality of Patient Clinican Communication About End-of-Life Care (QOC) score | ||||
Change History | Complete list of historical versions of study NCT00106080 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures ICMJE |
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 ] | ||||
Original Secondary Outcome Measures ICMJE |
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. | ||||
Current Other Outcome Measures ICMJE | |||||
Original Other Outcome Measures ICMJE | |||||
Descriptive Information | |||||
Brief Title ICMJE | Improving the Quality of End-of-Life Communication for Patients With COPD | ||||
Official Title ICMJE | Improving the Quality of End-of-Life Communication for Patients With COPD | ||||
Brief Summary | 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. |
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Detailed Description | 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 |
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Study Type ICMJE | Interventional | ||||
Study Phase | |||||
Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Investigator) |
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Condition ICMJE |
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Intervention ICMJE | 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. |
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Study Arm (s) |
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Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||
Recruitment Status ICMJE | Completed | ||||
Estimated Enrollment ICMJE | 400 | ||||
Completion Date | May 2008 | ||||
Primary Completion Date | May 2008 (final data collection date for primary outcome measure) | ||||
Eligibility Criteria ICMJE | 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
Exclusion Criteria:
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Gender | Both | ||||
Ages | 18 Years and older | ||||
Accepts Healthy Volunteers | No | ||||
Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
Location Countries ICMJE | United States | ||||
Administrative Information | |||||
NCT Number ICMJE | NCT00106080 | ||||
Other Study ID Numbers ICMJE | IIR 02-292 | ||||
Has Data Monitoring Committee | No | ||||
Responsible Party | Department of Veterans Affairs | ||||
Study Sponsor ICMJE | Department of Veterans Affairs | ||||
Collaborators ICMJE | |||||
Investigators ICMJE |
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Information Provided By | Department of Veterans Affairs | ||||
Verification Date | May 2008 | ||||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |