Advanced Cancer, Chronic Obstructive Pulmonary Disease (COPD), Congestive Heart Failure, End Stage Liver Disease, Restrictive Lung Disease
Conditions
Keywords
End-of-Life issues, Talking with your doctor, Coping with chronic illness
Brief summary
This research study is a randomized trial to evaluate a training program that is designed to improve the communication skills of clinicians. The training program focuses on care for patients with serious illnesses and their family members, and assesses effectiveness using patient and family outcomes. The long term goal of this research is to improve communication skills of doctors and nurses, thereby improving patient and family outcomes.
Detailed description
Three decades of research on end-of-life care in the United States indicates that people who are dying often spend their final days with a significant burden of pain and other symptoms and receive care they would not choose. Patient-clinician communication about end-of-life care is an important focus for improving patient-centered end-of-life care for three reasons: 1) it is an integral component of clinician skill that affects all other aspects of end-of-life care; 2) physicians and nurses in practice do not demonstrate adequate skills for communicating about end-of-life care; and 3) current training in end-of-life communication is inadequate. Studies have shown that clinicians can improve their communication skills with experiential training, but no studies to date have shown that an intervention to improve clinician communication skill improves patient outcomes. Furthermore, despite widespread knowledge that end-of-life care is best delivered in an interdisciplinary context, most studies do not incorporate interdisciplinary training that includes physicians and nurses. This is a randomized trial of a communication skills workshop for internal medicine residents and nurse practitioner (NP) students. A total of 373 residents and 128 NP students from two large training programs (UW and MUSC) will be randomized to either the intervention or usual education. The study's primary outcome measure will be the QOC scores on the communication about end-of-life care domain. The QOC will be assessed by patients, family members, and nurses before and after the intervention time period for all trainees. Secondary outcome measures are patient symptoms and patient-, family - and nurse-assessed QEOLC scores. Outcome measures will be collected for 5 patients and family members per trainee before the intervention period and 5 patients and family members per trainee after the intervention period. Process measures for both residents and NP students will include pre- and post-intervention assessment of knowledge, attitudes, and behavior regarding communication using standardized patient assessment as well as self-assessment and faculty assessment.
Interventions
BEHAVIORALTraining Program Intervention
Resident or NP Student receives the educational intervention during 8 half-day sessions.
Sponsors
National Institute of Nursing Research (NINR)
University of Washington
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Physician: * all internal medicine residents at either University of Washington (UW)or the Medical University of South Carolina * who have a clinical rotation allowing implementation of the intervention. NP Student: * All NP Students at UW or MUSC * in programs that train them to work with the following patient types: * Adult patents with Cancer or other chronic, life-limiting illnesses * Older Adults * Adults Primary Care Patients Patient: One or more of the following diagnostic criteria: * Advanced Cancer; * Chronic obstructive pulmonary disease (COPD) with FEV1 values \< 35% predicted and/or oxygen dependent; * Restrictive lung disease with a TLC \< 50% predicted; * Congestive heart failure with an ejection fraction \<30% or functional deficits matching New York Heart Association Class III or IV heart failure; * End stage liver disease including Child's Class C cirrhosis, MELD score ≥ 18, a variceal bleed, refractory ascites, or spontaneous bacterial peritonitis (SBP); * a Charlson Comorbidity Score point value ≥6; * in-patients with a University HealthSystem Consortium (UHC) Risk of Mortality score of major or extreme; * OR hospitalized patients ≥ 80 years. Family: * The ability to speak English well enough to be able to complete the study procedures * AND no significant dementia or delirium that would limit the family member's ability to complete instruments. Nurse-evaluators: * are working in the hospital or clinic with the resident or NP student enrolled in the study.
Exclusion criteria
* less than 18 years, * significant dementia, delirium, or psychosis; * the inability to speak English well enough to be able to complete the study procedures.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient and family ratings on the End-of-Life domain of the Quality of Communication Questionaire (QOC) | 4/1/2007-3/31/2012 |
Secondary
| Measure | Time frame |
|---|---|
| Patient symptoms of depression as assessed by the PHQ-8 (Memorial Symptom Assessment scale) | 4/01/2007-3/31/2012 |
| Patient-, family-, and nurse-assessed ratings of the quality of end-of-life care provided by study clinicians using Quality of End-of-Life Care questionaire | 4/01/2007-3/31/2012 |
Countries
United States
Outcome results
None listed