Wishes to Improve Support and Humanity at End-of-life in Safety-net Hospitals
WISHES
Personalized End of Life Care in Safety-Net Hospitals: Implementation of the 3 Wishes Project
2 other identifiers
interventional
900
1 country
4
Brief Summary
Dignified and compassionate end-of-life (EOL) care is a cornerstone of high-quality, patient-centered care, but in safety-net hospitals EOL care is often overlooked, considered too late, or not at all. By eliciting and implementing final wishes for dying patients, the 3 Wishes Project (3WP) has demonstrated, in tertiary academic centers, that acts of compassion can improve the EOL experience and help families cope with loss. The investigators propose to implement the 3WP in safety-net hospitals where there are less resources and more diverse, disadvantaged patient populations, and hypothesize that there will be similar positive effects on the EOL experience for patients, families, and clinicians.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2024
Longer than P75 for not_applicable
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 13, 2024
CompletedFirst Posted
Study publicly available on registry
February 26, 2024
CompletedStudy Start
First participant enrolled
March 19, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2028
April 22, 2026
April 1, 2026
4.4 years
February 13, 2024
April 21, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Families' assessment of the quality of end-of-life, particularly in emotional and spiritual support.
Bereaved families of patients who died in the ICU will complete an after-death survey, which includes the Bereaved Family Survey (BFS). The BFS asks questions regarding the family's perception of the patient's end of life care. We will also use a question from the FS-ICU (family satisfaction with ICU) to assess whether family felt supported in final hours of patient's life.
3 months after patient's death (families will be surveyed 3 months after the date of death).
Secondary Outcomes (3)
Family anxiety and depression
3 months after patient's death (families will be surveyed 3 months after the date of death).
Nurse Burnout
6 months and 1 year after
Family PTSD
3 months after patient's death (families will be surveyed 3 months after the date of death).
Study Arms (1)
3WP intervention
EXPERIMENTALfamilies of patients whose loved ones died in the ICU where the 3 Wishes Program has been implemented
Interventions
palliative care initiative in which clinicians elicits and implements small acts of kindness for dying patients and their families
Eligibility Criteria
You may qualify if:
- For participation in the 3WP, if there was a decision to withdraw life support or the health care team agreed that the patient's probability of dying in the hospital or on discharge to hospice was \>95% For surveys, next of kin/surrogate of a patient who died in the ICU during the study period For surveys, speaks English or Spanish
You may not qualify if:
- \<18 years old
- does not speak english or spanish
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of California, Los Angeleslead
- Olive View-UCLA Education & Research Institutecollaborator
- LAC+USC Medical Centercollaborator
- National Institute of Nursing Research (NINR)collaborator
Study Sites (4)
LA General Hospital
Los Angeles, California, 90033, United States
Ronald Reagan UCLA Medical Center
Los Angeles, California, 90095, United States
Olive View Medical Center
Sylmar, California, 91342, United States
Harbor-UCLA
Torrance, California, 90502, United States
Related Publications (6)
Neville TH, Clarke F, Takaoka A, Sadik M, Vanstone M, Phung P, Hjelmhaug K, Hainje J, Smith OM, LeBlanc A, Hoad N, Tam B, Reeve B, Cook DJ. Keepsakes at the End of Life. J Pain Symptom Manage. 2020 Nov;60(5):941-947. doi: 10.1016/j.jpainsymman.2020.06.011. Epub 2020 Jun 21.
PMID: 32574658BACKGROUNDVanstone M, Neville TH, Clarke FJ, Swinton M, Sadik M, Takaoka A, Smith O, Baker AJ, LeBlanc A, Foster D, Dhingra V, Phung P, Xu XS, Kao Y, Heels-Ansdell D, Tam B, Toledo F, Boyle A, Cook DJ. Compassionate End-of-Life Care: Mixed-Methods Multisite Evaluation of the 3 Wishes Project. Ann Intern Med. 2020 Jan 7;172(1):1-11. doi: 10.7326/M19-2438. Epub 2019 Nov 12.
PMID: 31711111BACKGROUNDVanstone M, Neville TH, Swinton ME, Sadik M, Clarke FJ, LeBlanc A, Tam B, Takaoka A, Hoad N, Hancock J, McMullen S, Reeve B, Dechert W, Smith OM, Sandhu G, Lockington J, Cook DJ. Expanding the 3 Wishes Project for compassionate end-of-life care: a qualitative evaluation of local adaptations. BMC Palliat Care. 2020 Jun 30;19(1):93. doi: 10.1186/s12904-020-00601-5.
PMID: 32605623BACKGROUNDCook DJ, Clarke FJ, Neville TH, Hoad N, Boyle A, Woods A, Dionne JC, Dennis BB, Toledo F, Tam B, Swinton M, Reid J, Vanstone M. The 3 Wishes Project: toward spiritual care at the end of life. Pol Arch Intern Med. 2023 Mar 29;133(3):16465. doi: 10.20452/pamw.16465. Epub 2023 Mar 29. No abstract available.
PMID: 36994496BACKGROUNDNeville TH, Taich Z, Walling AM, Bear D, Cook DJ, Tseng CH, Wenger NS. The 3 Wishes Program Improves Families' Experience of Emotional and Spiritual Support at the End of Life. J Gen Intern Med. 2023 Jan;38(1):115-121. doi: 10.1007/s11606-022-07638-7. Epub 2022 May 17.
PMID: 35581456BACKGROUNDNeville TH, Walling A, Wenger NS, Mittman BS, Tseng CH, Chang D, Cook D, Marentes Ruiz CJ, Cassano H, Beers E, Gadgil R, Kamangar N, Blake N, Tarn DM. Implementation and evaluation of the 3 Wishes Project in safety-net hospitals: Protocol for a hybrid effectiveness-implementation study. PLoS One. 2025 May 2;20(5):e0320843. doi: 10.1371/journal.pone.0320843. eCollection 2025.
PMID: 40315279DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
February 13, 2024
First Posted
February 26, 2024
Study Start
March 19, 2024
Primary Completion (Estimated)
August 1, 2028
Study Completion (Estimated)
August 1, 2028
Last Updated
April 22, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share