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RCT of ACP for Transplant

A Pilot Randomized Control Trial of Advance Care Planning and Triggered Palliative Care for Cancer Patients Undergoing Stem Cell Transplantation (RCT of ACP for Transplant)

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03158467
Enrollment
0
Registered
2017-05-18
Start date
2017-05-15
Completion date
2019-11-15
Last updated
2018-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer Patients Undergoing Stem Cell Transplantation (RCT of ACP for Transplant)

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.

Interventions

OTHERSurveys

Instruments will be administered via the online RedCAP platform. The survey instruments will include a Decision Conflict Scale (DCS), the McGill Quality of Life (MQoL), the Human Connection (THC), and a general demographics questionnaire. Patients will have the opportunity to complete the instruments via a research iPad while in clinic or via a survey link emailed to their private email account.

Sponsors

Abramson Cancer Center at Penn Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Number of surveys completed2 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026