- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06081660
Advance Care Planning for Older Latinos With Chronic Illness
Advance Care Planning for Older Latinos With Chronic Illness: A Feasibility Study
Study Overview
Status
Intervention / Treatment
Detailed Description
The goal of this study is to test the feasibility of a randomized controlled trial to learn about implementation of an intervention model, Advance Care Planning I Plan (ACP-I Plan), among older Latinos with chronic illnesses in community settings.
The questions of this study seek to explore implementation of the intervention model:
- To evaluate feasibility, acceptability, and preliminary impact of ACP-I Plan to improve AD documentation and increase engagement in ACP communication with family and providers among older Latinos with chronic diseases (cancers and non-cancers); and
- To evaluate implementation of ACP-I Plan in a community setting and examine further need for adaption.
Participants will be randomized into two groups:
ACP education consisting of
- a brief social work screening,
- an educational pamphlet,
- advance directive forms (in English and Spanish), and
- community resource materials (i.e., handout); and
ACP education plus counseling consisting of
- motivational interviewing
- decisional support, and
- patient navigation to address barriers We anticipate that ACP-I Plan will be feasibly and acceptable. Participants who receive ACP-I Plan will show 1) greater likelihood of documenting an AD, 2) greater importance of and concern for engaging in ACP communication with family members and providers, and 3) reduced distress at 4-week post intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
San Diego, California, United States, 92182
- San Diego State University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 50 years old or older
- Latino/Latina or Hispanic?
- Have 1 or more chronic health conditions
Exclusion Criteria:
- Schizophrenia
- Schizoaffective Disorder
- Dementia
- Alzheimer's disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: ACP education
ACP education consisting of
|
ACP-I Plan consisting of education, counseling, decisional support, and patient navigation
|
|
Experimental: ACP education plus counseling
ACP education plus counseling consisting of
|
ACP-I Plan consisting of education, counseling, decisional support, and patient navigation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intervention Feasibility
Time Frame: 12 months
|
Feasibility We use benchmarks for feasibility.
|
12 months
|
|
Satisfaction with intervention
Time Frame: 1 month
|
Acceptability of the intervention Satisfaction survey questions includes 14 questions using "I" statements and a 5-point Likert scale: Strongly Disagree to Strongly Agree). Improved scores at follow up indicate satisfaction of information delivery. Reference Lyon ME, Garvie PA, Briggs L, He J, McCarter R, D'Angelo LJJJopm. Development, feasibility, and acceptability of the Family/Adolescent-Centered (FACE) Advance Care Planning intervention for adolescents with HIV. 2009;12(4):363-372. |
1 month
|
|
Retention and Attrition Rates
Time Frame: 12 months
|
Feasibility of recruitment and retention
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Completion Rates
Time Frame: 1 month
|
Self report yes/no completed an advance directive document. We use the method that Douglas & Brown (2002) used ask about completion of advance directives at 2 points, baseline and 1-month follow-up. Questions have yes/no [Y/N], responses. Reference Douglas R, Brown HN. Patients' attitudes toward advance directives. Journal of Nursing Scholarship. 2002;34(1):61-65. We also use the Advance Directive Attitude Survey (ADAS) by Nolan has 16 items and asks questions (uses a 4-point Likert scale, Strongly Agree to Strongly Disagree with AD decision making). Sixteen questions are subscales and ask about: (a) opportunity for treatment choices, (b) effect of advance directives on the family, (c) effect of an AD on treatment, and (d) perception of illness. Nolan MT, Bruder M. Patients' attitudes toward advance directives and end-of-life treatment decisions. Nursing outlook. 1997;45(5):204-208. |
1 month
|
|
Communication Readiness Provider
Time Frame: 1 month
|
Barriers to ACP communication and readiness to talk with provider. We use a barrier scale developed to identify Barriers to Communication about Advance Care Planning (Nedjat-Haiem, 2022) which has 19 questions and uses a scale from 0 to 4, asking how much of a concern is this for you? Readiness to engage in communication about ACP will be assessed by three yes/no questions that ask about: (1) fear of death and dying, (2) difficulty engaging in EOL care communication, and (3) worry about illness severity. We also use a readiness scale (1-10) which asks: how ready are you to engage in ACP communication with your physician. |
1 month
|
|
Communication Readiness Family
Time Frame: 1 month
|
Self Report yes/no - Readiness to talk with a family member We also use one question to ask about about readiness using a scale (1-10) which asks: how ready are you to engage in ACP communication with your family member? |
1 month
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayala, PhD, San Diego State University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS-2020-0175
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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