Chronic Disease Clinical Trial
— PREPAREOfficial title:
Improving Advance Care Planning by Preparing Diverse Seniors for Decision Making
Verified date | October 2018 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this proposal is to test whether a multi-media website (www.prepareforyourcare.org) that is focused on preparing older adults for communication and medical decision making can help people engage in advance care planning.
Status | Completed |
Enrollment | 541 |
Est. completion date | November 2017 |
Est. primary completion date | November 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 55 Years and older |
Eligibility |
Inclusion Criteria: - English-speaking older adults (=55 years) - = 2 chronic illnesses determined by International Classification of Diseases-9 (ICD-9) codes - = 2 visits with an outpatient primary care clinician at San Francisco General Hospital in the past year - =2 additional outpatient/inpatient visits to San Francisco General Hospital in the past year Exclusion Criteria: - deaf, blind, or demented as determined by ICD-9 codes - too mentally or physically ill to participate as determined by their clinicians - Moderate or severe cognitive impairment as determined by the Short Portable Mental Status Questionnaire (SPMSQ), and mild cognitive impairment as determined by the SPMSQ plus an abnormal Mini-Cog - self-reported poor vision and inability to see the words on a newspaper - lack of a telephone - traveling or moving out of the area for =3 months during the study follow- up period |
Country | Name | City | State |
---|---|---|---|
United States | San Francisco General Hospital and Trauma Center | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | National Institute on Aging (NIA) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | New advance care planning documentation in the medical record | The primary outcome is documentation of ACP wishes in the medical record. ACP documentation for the purposes of this study includes legal advance directive forms or other documentation of patients wishes for medical care in clinical notes. | 15 months after study enrollment | |
Secondary | Self-reported engagement in advance care planning behaviors | Secondary outcomes were chosen to measure the full process of ACP. Using validated questionnaires, we will measure ACP behavior change processes, such as knowledge, contemplation, self-efficacy, and readiness, as well as several ACP actions, such as identifying a surrogate decision maker, identifying values and goals for medical care, choosing the level of leeway in surrogate decision making, discussing one's wishes with clinicians and surrogates, and documenting one's wishes in an advance directive. | 12 months from baseline |
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