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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06247215
Other study ID # 2023-0354
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 15, 2024
Est. completion date March 31, 2025

Study information

Verified date May 2024
Source University of Illinois at Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Less than 15% of Chinese Americans complete advance directives. That is less than half of the 37% completion rate in the US general population. This disparity in the use of advance care planning between White Americans and Chinese Americans may extend to disparities in end-of-life care. To address such disparities in end-of-life care, we will develop and assess the acceptability of a culturally tailored resilience-building intervention to help Chinese Americans with cancer or heart disease and their family caregivers engage in advance care planning discussions.


Description:

The overall objective of this cross-sectional pilot study is to develop a culturally tailored resilience-building intervention for Chinese Americans with cancer or heart disease in Chicago. A qualitative analysis of semi-structured interviews will be conducted to identify how religious leaders addressed death-related topics with Chinese Americans with cancer or heart disease in Chicago. In addition, a usability test of a resilience-building intervention prototype will be conducted to to understand the feasibility and acceptability among 18 pairs of Chinese Americans and their family caregivers (9 pairs with cancer and 9 pairs with heart disease).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 36
Est. completion date March 31, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion criteria for patient participants: - Age = 18 years of age - Having a cancer diagnosis or a heart failure diagnosis documented in the electronic medical record - Being able to read and respond to questions in English or Mandarin - Having a family caregiver who is responsible for the care and willing to participate in the study - Being of non-Hispanic Asian race/ethnicity Exclusion criteria for patient participants: - Having cognitive impairment per a Short Portable Mental Status Questionnaire with more than 3 errors - Having received heart transplantation or a left ventricular assist device • Having completed an advance directive - Being born in the US Inclusion criteria for identified family caregivers: - Age = 18 years - Being able to read and respond to questions in English or Mandarin - Being identified by the patient as a family caregiver

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Culturally tailored resilience-building intervention
A booklist teaching resilience skills for advance care planning discussions

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
University of Illinois at Chicago Rush University Medical Center, University of Chicago

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability The Theoretical Framework of Acceptability, which ranges from 1 to 5, will be used to assess acceptability. A higher score indicates higher acceptability. Immediately at the end of the usability testing
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