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Virtual Dignity Therapy for Palliative Care Patients With Advanced Cancer

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05113199
Enrollment
21
Registered
2021-11-09
Start date
2021-11-18
Completion date
2025-02-17
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Cancer

Keywords

Dignity Therapy

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.

Interventions

BEHAVIORALVirtual Dignity Therapy

Virtual Dignity Therapy will be facilitated by a registered nurse or medical doctor trained in Dignity Therapy.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Feasibility Number2 YearsStudy feasibility will be measured by the number of participants who enrolled and finished the study.
AcceptabilityWeek 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026