Skip to main content
Clinical Trials/NCT05113199
NCT05113199
Completed
Not Applicable

Feasibility and Acceptability of Virtual Dignity Therapy for Palliative Care Patients with Advanced Cancer

Mayo Clinic1 site in 1 country21 target enrollmentNovember 18, 2021
ConditionsAdvanced Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advanced Cancer
Sponsor
Mayo Clinic
Enrollment
21
Locations
1
Primary Endpoint
Feasibility Number
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to determine if it is feasible and acceptable to recruit for and deliver the Virtual Dignity Therapy intervention to palliative care patients with advanced cancer.

Detailed Description

This study is an investigator-initiated, single site Mayo Clinic Rochester prospective minimal risk pilot study to determine feasibility and acceptability of Virtual Dignity Therapy. The Dignity Therapy intervention is a brief, individualized psychotherapy that aims to relieve psycho-emotional and existential distress and improve the experiences of patients whose lives are impacted by serious illness. This therapy offers patients an opportunity to reflect on their life with a trained facilitator and share their thoughts and memories with family and other people in their life. This therapy consists of a total of 3 sessions, with each session 2-4 weeks apart, in which the investigator provides questions focused on life review. The sessions are recorded and transcribed. The interventionist will work with patients to edit the document and provide a final generativity document for patient to keep and give to loved ones.

Registry
clinicaltrials.gov
Start Date
November 18, 2021
End Date
February 17, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Deirdre R. Pachman

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years
  • English fluency
  • No diagnosed dementia
  • Diagnosis of advanced cancer
  • Expected prognosis \> 6 months
  • Provide informed consent
  • Ability to complete questionnaire(s) by themselves or with assistance

Exclusion Criteria

  • Other psychological co-morbidities such as untreated schizophrenia, bipolar disease
  • Recent suicide attempt or psychiatric illness severe enough that hospitalization has been necessary in last 6 months
  • Active delirium
  • Participation in concurrent legacy offerings through the palliative care clinic
  • Inclusion Criteria for caregivers:
  • Age ≥18 years
  • English fluency
  • Provide informed consent
  • Supported patient through Dignity Therapy

Outcomes

Primary Outcomes

Feasibility Number

Time Frame: 2 Years

Study feasibility will be measured by the number of participants who enrolled and finished the study.

Acceptability

Time Frame: Week 8 (after 3rd intervention session)

Acceptability, as measured by the 7-item Was it Worth It (WIWI Questionnaire).The questions are answered as either "yes, no, or uncertain," overall perception of quality of life change, overall perception of study experience, one open-ended feedback question, and an option to talk with someone about concerns. Positive responses indicate acceptability. Results are reported as individual items.

Study Sites (1)

Loading locations...

Similar Trials