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Clinical Trials/NCT05433090
NCT05433090
Completed
N/A

An Inpatient Advance Care Planning Intervention for Older Patients With Hematologic Malignancies

University of Rochester1 site in 1 country41 target enrollmentNovember 23, 2022

Overview

Phase
N/A
Intervention
Inpatient serious illness care program
Conditions
Hematologic Malignancies
Sponsor
University of Rochester
Enrollment
41
Locations
1
Primary Endpoint
Retention Rate
Status
Completed
Last Updated
2 months ago

Overview

Brief Summary

This is a pilot study to assess the preliminary efficacy of an inpatient advance care planning intervention on outcomes in older patients with hematologic malignancies

Detailed Description

Older adults with hematologic malignancies receive more aggressive inpatient care at the end of life compared to patients with solid tumors. Advance care planning may promote early serious illness conversations for patients with hematologic malignancies, leading to less aggressive healthcare utilization at the end of life. This pilot aims to assess the preliminary efficacy of an inpatient advance care planning intervention on outcomes in older patients with hematologic malignancies.

Registry
clinicaltrials.gov
Start Date
November 23, 2022
End Date
November 14, 2024
Last Updated
2 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kah Poh Loh

Associate Professor - Department of Medicine, Hematology/Oncology (SMD)

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • Age ≥60 years
  • A diagnosis of hematologic malignancy \[including but not limited to acute leukemia, myeloid malignancies (e.g., atypical CML, MDS/MPN overlap syndromes, CMML), multiple myeloma, lymphoma, or any other hematologic malignancies based on the primary oncologist's judgment\]
  • Able to provide informed consent
  • Being managed in the inpatient setting
  • English-speaking

Exclusion Criteria

  • Not provided

Arms & Interventions

Experimental

Patients will participate in an inpatient advance care planning intervention.

Intervention: Inpatient serious illness care program

Outcomes

Primary Outcomes

Retention Rate

Time Frame: From consent until completion of the ACP intervention visit, usually within 1 week.

Retention rate is the percentage of consented patients who completed the ACP intervention visit. A retention rate of \>70% was considered feasible.

Secondary Outcomes

  • Advance Directive Completion - HCP(From baseline (pre-intervention) to 1 year post-intervention. The time interval is approximately 1 year.)
  • Advance Directive Completion - MOLST(From baseline (pre-intervention) to 1 year post-intervention. The time interval is approximately 1 year.)

Study Sites (1)

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