Acute Myeloid Leukemia Clinical Trial

Home Away From Home – Quality of Life Surveys

Summary

Treatment for pediatric acute myeloid leukemia (AML) involves intensive chemotherapy regimens that result in periods of profound neutropenia leaving patients susceptible to severe infectious complications. Infectious complications are the leading cause of treatment related mortality among AML patients, but there are little clinical data to inform whether management of neutropenia post AML chemotherapy should occur in an outpatient or inpatient setting. Further, no studies have been conducted that assess the impact of neutropenia management strategy on the quality of life of pediatric patients with AML and their caregivers.

View Full Description

Full Description

This is a prospective observational cohort study, where the primary objective of this study is to compare patient and caregiver quality of life and other patient-centered outcomes for inpatient versus outpatient management of neutropenia in children with AML or MDS receiving standard intensive AML frontline chemotherapy.

Local study investigators (pediatric oncologists and study coordinators) at each of the fifteen participating pediatric institutions will communicate on a weekly basis with their inpatient leukemia service to identify AML or MDS patients potentially eligible for study enrollment. Once identified, study personnel will review each patient for study eligibility criteria. Three visits with the patient and their caregivers will occur: a screening visit, initial survey visit, and a follow-up visit.

Screening Visit: The eligibility criteria for participation will be confirmed prior to approaching for consent. Eligible patients interested in the study will be approached for consent at any time from AML/MDS diagnosis through last day of chemotherapy in the treatment course under study. In some cases, the patient's caregivers may not be present in the hospital to provide consent. In these cases, study personnel will obtain verbal consent from the caregivers and child assent (if appropriate).

Visit 1 will occur prior to the last day of chemotherapy administration in the course. This visit will include:

2 Brief demographic surveys to capture covariates unavailable in the medical record
Baseline health-related quality of life (HRQOL) surveys
A baseline financial toxicity assessment

Surveys will be administered via paper or a smart device and will last a total of 15-30 minutes per respondent. In the case that the child is 5 years of age or older, the child self-report and parent proxy-report scales will be separately administered to the child and caregiver, respectively. If the child is under 5 years of age, only the parent-proxy version will be administered. Only the caregiver completes the baseline financial toxicity assessment. We will provide a $25 gift card to each child-parent dyad upon completion of the baseline surveys

Visit 2 will occur within the period after absolute neutrophil count recovery and ideally prior to the start of the subsequent course of chemotherapy, but no later than the last day of chemotherapy in that next treatment course. This visit will include:

Follow-up HRQOL surveys
Patient-centered outcome survey developed previously from qualitative interviews of AML patients and their caregivers
A follow-up financial toxicity assessment

Surveys will be administered via paper or a smart device and will last a total of 15-30 minutes per respondent. In the case that the child is 5 years of age or older, the child self-report and parent proxy-report scales will be administered to the child and caregiver, respectively. If the child is under 5 years of age, only the parent-proxy version will be administered. The follow-up financial toxicity assessment and the patient-centered outcome survey are completed by the caregiver only. We will provide a $25 gift card to each child-parent dyad upon completion of the follow-up surveys.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Participants will be enrolled as patient-caregiver dyads. The patient must be:

Less than 19 years of age at diagnosis.
Patient is English or Spanish literate.
Receiving chemotherapy for AML between June 1, 2016 and December 31, 2019.

Participants will be enrolled as patient-caregiver dyads. The caregiver must be:

English or Spanish literate.
The legal guardian of a patient receiving chemotherapy for AML between June 1, 2016 and December 31, 2019.
Parental/caregiver informed consent and, if appropriate, child assent.

Exclusion Criteria:

Patients being treated for relapsed AML
Patients with Acute Promyelocytic Leukemia (APML)
Patients undergoing stem cell transplant (SCT)
Patients receiving reduced intensity frontline chemotherapy

Study is for people with:

Acute Myeloid Leukemia

Estimated Enrollment:

154

Study ID:

NCT02777021

Recruitment Status:

Completed

Sponsor:

Children's Hospital of Philadelphia

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 15 Locations for this study

See Locations Near You

Arkansas Children's Hospital
Little Rock Arkansas, 72202, United States
Lucile Packard Children's Hospital
Palo Alto California, 94304, United States
Children's Hospital of Colorado
Aurora Colorado, 80045, United States
Nemours/Alfred I DuPont Hospital for Children
Wilmington Delaware, 19803, United States
Children's Healthcare of Atlanta
Atlanta Georgia, 30322, United States
Ann & Robert H Lurie Children's Hospital of Chicago
Chicago Illinois, 60611, United States
Dana-Farber Cancer Institute/Boston Children's Hospital
Boston Massachusetts, 02215, United States
C.S. Mott Children's Hospital
Ann Arbor Michigan, 48109, United States
Children's Hospital of Michigan
Detroit Michigan, 48201, United States
Children's Hospital of Philadelphia
Philadelphia Pennsylvania, 19104, United States
St. Jude Children's Research Hospital
Memphis Tennessee, 38105, United States
Children's Medical Center of Dallas
Dallas Texas, 75235, United States
Texas Children's Hospital
Houston Texas, 77030, United States
Primary Children's Hospital
Salt Lake City Utah, 84132, United States
Seattle Children's Hospital
Seattle Washington, 98105, United States

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Estimated Enrollment:

154

Study ID:

NCT02777021

Recruitment Status:

Completed

Sponsor:


Children's Hospital of Philadelphia

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider