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RCT of ACP for Transplant

Withdrawn
Conditions
Cancer Patients Undergoing Stem Cell Transplantation (RCT of ACP for Transplant)
Interventions
Other: Surveys
Registration Number
NCT03158467
Lead Sponsor
Abramson Cancer Center at Penn Medicine
Brief Summary

We aim to examine the effect of an online advance directive on decisional conflict and quality of life in patients undergoing stem cell transplant. We also aim to assess the effect of palliative care at the time of a sentinel event on quality of life.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

The inclusion criteria for Phase I (primary objective) are as follows:

  • Age ≥ 18 years
  • Hematologic malignancy diagnosis including any subset of myeloma, lymphoma, leukemia, or myelodysplastic syndrome
  • Currently scheduled for autologous or allogeneic transplant at the Hospital of the University of Pennsylvania

The inclusion criteria for Phase II (secondary objective) are as follows:

  • Age ≥ 18 years
  • Hematologic malignancy diagnosis including any subset of lymphoma, leukemia, or myelodysplastic syndrome
  • Received an autologous or allogeneic stem cell transplant at the Hospital of the University of Pennsylvania and experienced a sentinel event of either 1) disease relapse,2) severe (Grade III or IV) graft-versus-host disease, or 3) unplanned hospital admission with length of stay greater than 72 hours.
Exclusion Criteria

The exclusion criteria for Phase I include:

  • Inability to read and write English
  • Not serving as the primary decision maker for their health-related decisions
  • Having a non-hematologic malignancy reason for undergoing transplantation (e.g. aplastic anemia)

The exclusion criteria for Phase II include:

  • Not completing participation in Phase I of the study
  • Myeloma diagnosis

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Phase 1Surveys-
Phase 2Surveys-
Primary Outcome Measures
NameTimeMethod
Number of surveys completed2 years
Secondary Outcome Measures
NameTimeMethod
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