Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

AI-assisted personalized legacy program — Reflections: My Story

Official title: Feasibility and Acceptability of AI Assisted Personalized Legacy Program (Reflections: My Story) for Patients With Serious Illness

Run by Mayo Clinic · NCT07009210 · Data updated 2026-11-12

This AI-assisted personalized legacy program tries to help adults with serious illness reflect on their life and create a keepsake document to share with loved ones.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorMayo Clinic
Academic / other
Locations2 sites (Phoenix, Arizona and 1 other locations)
StatusRecruiting
StartedAugust 11, 2025
Main results expectedDecember 31, 2026
Study endsJune 30, 2027
Registry record updatedJune 17, 2026
Trial IDNCT07009210 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (age ≥18) with a serious illness who are English-fluent, can provide informed consent, and can complete questionnaires with or without assistance are the intended participants.

Probably not a fit

Patients with active delirium, advanced dementia, untreated severe psychiatric disorders (such as untreated schizophrenia or bipolar disorder), recent psychiatric hospitalization, or those already receiving concurrent legacy services are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a multi-site, minimal-risk pilot conducted at Mayo Clinic to test feasibility and acceptability of a brief, individualized psychotherapy called the AI Assisted Personalized Legacy Program. Patients meet with a trained facilitator to reflect on life memories and values while sessions are recorded and transcribed. The interventionist and patient work together to edit the transcript into a polished legacy document that the patient can keep and share. The pilot will document recruitment, delivery, participant feedback, and preliminary signals of emotional or existential benefit.

Why it matters

Potential benefit: If successful, the program could reduce existential and psycho-emotional distress and improve patient and family experience by producing a meaningful, shareable legacy document.

How similar studies have gone: Non-AI life-review and legacy interventions in palliative care have shown promising reductions in existential distress and improved family satisfaction, but AI-assisted personalized legacy programs are relatively novel and less well tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Participant population: Adults with serious illness - defined as a health condition that carries a high risk of mortality

Inclusion Criteria for patients:

1. Age ≥18 years
2. English fluency
3. Provide informed consent
4. Ability to complete questionnaire(s) by themselves or with assistance

Exclusion Criteria:

1. Other psychological co-morbidities such as untreated schizophrenia, bipolar disease
2. Recent suicide attempt or psychiatric illness severe enough that hospitalization has been necessary in last 6 months
3. Active delirium
4. Advanced dementia
5. Participation in concurrent legacy offerings through the palliative care clinic

Where it's running

  • Mayo Clinic
    Phoenix, Arizona, United States
    Recruiting
  • Mayo Clinic
    Rochester, Minnesota, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.