Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to determine if it is feasible and acceptable to recruit for and deliver the AI Assisted Personalized Legacy Program intervention to patients with serious illness.
This study is an investigator-initiated, multi-site Mayo Clinic prospective minimal risk pilot study to determine feasibility and acceptability of an AI Assisted Personalized Legacy Program. The AI Assisted Personalized Legacy Program 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. The sessions are recorded and transcribed. The interventionist will work with patients to edit the document and provide a final legacy document for patient to keep and give to loved ones.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AI Assisted Personalized Legacy Program | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AI Assisted Personalized Legacy Program | Behavioral | AI Assisted Personalized Legacy Program will be facilitated by a clinician trained in legacy work. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility Number | Study feasibility will be measured by the number of participants who enrolled and finished the study. | 2 years |
| Acceptability | 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. | 5-10 days post-delivery of the final legacy document |
Not provided
Not provided
Participant population: Adults with serious illness - defined as a health condition that carries a high risk of mortality
Inclusion Criteria for patients:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Melissa Felt | Contact | 507-255-4162 | felt.melissa@mayo.edu | |
| Dept. of Medicine Research Hub | Contact | 507-266-1944 | DOMResearchHub@mayo.edu |
| Name | Affiliation | Role |
|---|---|---|
| Deirdre Pachman, MD | Mayo Clinic in Rochester | Principal Investigator |
| Mark Edwin, MD | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic | Recruiting | Phoenix | Arizona | 85054 | United States |
Not provided
| Label | URL |
|---|---|
| Mayo Clinic Clinical Trials | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Mayo Clinic | Recruiting | Rochester | Minnesota | 55905 | United States |
|