About this trial

This research study is evaluating to examine the efficacy of a novel a self-administered digital application (DREAMLAND) for improving patients' long-term quality of life and psychological outcomes for patients with acute myeloid leukemia undergoing intensive chemotherapy.

Eligibility criteria

Qualifiers

Hospitalized patients (age > 18 years) with a diagnosis of AML.

Initiating treatment with either a) intensive chemotherapy (7+3) or modification of this regimen on a clinical trial, or a similar intensive regimen or b) hypomethylating agents (HMA) +/- additional agents or modification of this regimen on a clinical trial.

Ability to comprehend and speak English as the digital apps are only available in English

Disqualifiers

Patients with a diagnosis of acute promyelocytic leukemia

Patients with acute or unstable psychiatric or cognitive conditions which the treating clinicians believes prohibits informed consent or compliance with study procedures.

Trial design

Treatments tested in this trial

  • DREAMLAND
  • VITAL WELLNESS

Treatment groups

200 Participants
are divided into 2 treatment groups

Locations

3
Massachusetts General Hospital (MGH)02114, BostonMassachusetts, United States
Duke University27710, DurhamNorth Carolina, United States
Fred Hutchinson Cancer Research Center (FHCRC)98109, SeattleWashington, United States

Sponsors and collaborators

Massachusetts General Hospital

Lead sponsor

National Cancer Institute (NCI)

Collaborator