Home › Acute Myeloid Leukemia › NCT06472128
Novel Digital Application for Patients With Acute Leukemia
Recruiting
Multi-Site Randomized Controlled Trial of a Novel Digital Application (DREAMLAND) to Improve Outcomes for Patients With Acute Myeloid Leukemia
Who can join
Ages 18 to 120 · All sexes
Full eligibility criteria
Inclusion Criteria: * 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 Note: Patients newly diagnosed as well as those with relapsed/refractory AML initiating treatment with intensive or HMA-based chemotherapy will be eligible to participate. Exclusion Criteria: * 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.
About the study
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.
What is being tested
- DREAMLAND (behavioral)
- VITAL WELLNESS (behavioral)
Sponsor: Massachusetts General Hospital · Participants: 200 · Started: Oct 21, 2024
Contact the study team
- Areej El-Jawahri, MD · Phone: 617-724-4000
Official record on ClinicalTrials.gov — NCT06472128
Locations in the U.S.
| Massachusetts | Massachusetts General Hospital (MGH), Boston |
| North Carolina | Duke University, Durham (Not yet recruiting) |
| Washington | Fred Hutchinson Cancer Research Center (FHCRC), Seattle (Not yet recruiting) |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.