A Decisional Intervention for Older Adults With Acute Myeloid Leukemia and Their Caregivers
About this study
This is a multicenter randomized controlled trial that assesses the efficacy of a decisional intervention \[University of Rochester-Geriatric Oncology assessment for Acute myeloid Leukemia (UR-GOAL)\] compared to an attention control.
- Condition
- Oncology, Myeloid Leukemia, Acute, Cancer
- Tested
- UR-GOAL
- Sponsor
- University of Rochester
Who can join
- Age
- 60 years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
Inclusion 23
- Minimum age: 60 years
- Study condition: Oncology, Myeloid Leukemia, Acute, Cancer
- Patients
- Age ≥60 years (from date of consent, confirmed on electronic medical records)
- A new diagnosis of AML
- Diagnosis can be based on the International Consensus Classification or World Health Organization
- Myeloid sarcoma is allowed
- AML with central nervous system involvement is allowed
- Cancer-directed treatment has not started
- Treatment to temporarily decrease white blood cells is acceptable; these may include hydroxyurea, leukapheresis, or cytarabine
- Intrathecal chemotherapy is acceptable
- The patient's oncologist has been or will be enrolled on the study
- English or Spanish-speaking
- Patients without a caregiver will still be eligible to participate in the study Exclusion criteria
- A diagnosis of acute promyelocytic leukemia
- Patients with psychiatric or cognitive conditions which the treating oncologist believes prohibits informed consent or compliance with study procedures
- Prior cancer-directed treatment for AML
- Caregivers
- Selected by the patient when asked if there is a "family member, partner, friend or caregiver \[age 18 or older\] with whom you discuss or who can be helpful in healthrelated matters."
- Caregiver may be paid/professional or informal caregiver
- Able to provide informed consent
- Oncologists
- Oncologists caring for patients with AML Exclusion criteria
Where
4 sites, 4 recruiting
University of Alabama at Birmingham, Division of Hematology and Oncology
Birmingham, Alabama, United States
University of North Carolina Lineberger Comprehensive Cancer Center
Chapel Hill, North Carolina, United States
University of Rochester Medical Center
Rochester, New York, United States
Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Section of Hematology/Oncology
Winston-Salem, North Carolina, United States
Contact
-
Kah Poh Loh
585-276-4353 Kahpoh_Loh@URMC.Rochester.edu
-
Becky Gravenstede
585-727-4728 becky_gravenstede@urmc.rochester.edu
Potential match only. Final eligibility is determined by the study team.