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Clinical Trials/NCT06061965
NCT06061965
Completed
Not Applicable

Facilitating Advance Care Planning Discussions Between Patients With Advanced Cancer and Their Family Caregivers Using a Resilience-Building Intervention

University of Illinois at Chicago1 site in 1 country36 target enrollmentJuly 9, 2024

Overview

Phase
Not Applicable
Intervention
Web-based resilience-building intervention
Conditions
Resilience, Psychological
Sponsor
University of Illinois at Chicago
Enrollment
36
Locations
1
Primary Endpoint
Usability
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

The aims of this study are to (1) identify the advance care planning deliberation process among 20 dyads of patients with advanced cancer and family caregivers and (2) conduct usability testing among 9 dyads to refine the content and design of the web-based resilience-building intervention.

Detailed Description

Patients with advanced cancer have not fully benefited from advance care planning due to the high levels of anxiety and depression experienced and other barriers that affect their appraisals and coping. Despite the protective effects of resilience, there have been few clinical trials improving the resilience skills of patients with advanced cancer and their family caregivers to help initiate advance care planning discussions and sustain engagement. This research will provide new insights through using a dyadic intervention approach to advance care planning while developing and evaluating a web-based resilience-building intervention to improve the completion of advance directives, resilience, coping, anxiety, and depression for patients with advanced cancer and their family caregivers.

Registry
clinicaltrials.gov
Start Date
July 9, 2024
End Date
May 22, 2025
Last Updated
3 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients will be eligible for the study if they (1) are ≥ 18 years of age; (2) have a cancer diagnosis; (3) are able to read and respond to questions in English with minimal assistance from family caregivers for interpretation; (4) have previously completed an advance directive such as a living will; (5) have a family caregiver who serves as a surrogate in the advance directive and is willing to participate in the study; and (6) have access to the internet on a cell phone, laptop, or computer.
  • Family caregivers will be eligible if they (1) are ≥ 18 years of age; (2) are able to read and respond to questions in English with minimal assistance from others for interpretation; (3) are identified by the patient as a family caregiver who serves as a surrogate for health care decisions; and (4) have access to the internet on a cell phone, laptop, or computer.

Exclusion Criteria

  • Patients who have cognitive impairment per a Short Portable Mental Status Questionnaire score \< 8.

Arms & Interventions

Web-based resilience-building

The web-based resilience-building intervention will be implemented on a website and consist of (1) assessments to help participants (a) understand their coping strategies and (b) appraise their beliefs, values, and goals about advance care planning and (2) 6 weekly modules.

Intervention: Web-based resilience-building intervention

Outcomes

Primary Outcomes

Usability

Time Frame: Immediately at the end of the usability testing

Qualitative feedback from participants about the impressions of the website prototype

Study Sites (1)

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