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Clinical Trials/NCT06081660
NCT06081660
Completed
N/A

Advance Care Planning for Older Latinos With Chronic Illness: A Feasibility Study

San Diego State University1 site in 1 country24 target enrollmentSeptember 14, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Patient Engagement
Sponsor
San Diego State University
Enrollment
24
Locations
1
Primary Endpoint
Retention and Attrition Rates
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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.

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: 1. 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 2. To evaluate implementation of ACP-I Plan in a community setting and examine further need for adaption. Participants will be randomized into two groups: 1. 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 2. 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.

Registry
clinicaltrials.gov
Start Date
September 14, 2022
End Date
April 16, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Frances Nedjat-Haiem

Associate Professor

San Diego State University

Eligibility Criteria

Inclusion Criteria

  • 50 years old or older
  • Latino/Latina or Hispanic?
  • Have 1 or more chronic health conditions

Exclusion Criteria

  • Schizophrenia
  • Schizoaffective Disorder
  • Alzheimer's disease

Outcomes

Primary Outcomes

Retention and Attrition Rates

Time Frame: 12 months

Feasibility of recruitment and retention

Intervention Feasibility

Time Frame: 12 months

Feasibility We use benchmarks for feasibility. 1. Number of Participants Recruited, and screening no more than 100 participants, 2. tracking numbers of participants consented into the study, 3. percent refused to participate and dropout, amount of time to screen participants and complete a baseline survey once consented into the study, 4. ACP-I Plan intervention delivered for the first session \<2 weeks from their recruitment and randomization date and second session \<4 weeks from recruitment, 5. identify missing data. 6. Track the number of participants who indicate they returned a completed AD to their provider and/or talked with a family member regarding ACP.

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.

Secondary Outcomes

  • Communication Readiness Provider(1 month)
  • Completion Rates(1 month)
  • Communication Readiness Family(1 month)

Study Sites (1)

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