Brief Summary

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.

Trial Health

On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment

participants targeted

Target at P25-P50 for not_applicable

Timeline

13mo left

Started Aug 2025

Typical duration for not_applicable

Geographic Reach

1 country

2 active sites

Status

recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

1.8 years study duration

Study Progress41%

Aug 2025Jun 2027

First Submitted

Initial submission to the registry

May 29, 2025

Completed

8 days until next milestone

First Posted

Study publicly available on registry

June 6, 2025

Completed

2 months until next milestone

Study Start

First participant enrolled

August 11, 2025

Completed

1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected

6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

September 16, 2025

Status Verified

September 1, 2025

Enrollment Period

1.3 years

First QC Date

May 29, 2025

Last Update Submit

September 10, 2025

Conditions

Serious Illness Existential Distress

Keywords

Legacy Work

Outcome Measures

Primary Outcomes (2)

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

Study Arms (1)