This is a randomized clinical trial to determine whether a psychosocial intervention (BMT-CARE) is effective at improving the quality of life and reducing psychosocial distress of caregivers and patients treated with hematopoietic cell transplant (HCT). The BMT-CARE intervention was developed with the goal of improving the experience and needs of caregivers of patients treated with HCT.
Caregivers will be randomized into one of the two study groups: BMT-CARE plus usual care, or usual care.
Participation in this study is expected to last up to 180 days after HCT.
Investigators expect that about 400 caregivers and up to 400 patients treated with HCT will take part in this research study.
The National Institutes of Health is supporting this research by providing funding.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adult caregivers (≥18 years) relative or friend of a patient identified as living with them or having in-person contact with them at least twice a week.
Caregiver of a patient receiving allogeneic or autologous HCT for the treatment of cancer.
Ability to read and respond to survey questions in English, Spanish or with minimal assistance from an interpreter.
Adult patients (≥18 years) with a hematologic malignancy and planned admission for autologous or allogeneic HCT.
Ability to respond to questions in English, Spanish, or with minimal assistance from an interpreter.
You may not be if
Caregivers of patients undergoing HCT for a benign hematologic condition or undergoing outpatient HCT.
Caregivers with a major untreated psychiatric or cognitive condition which the treating oncology clinicians believes interferes with the capacity to provide informed consent.
Caregivers of patients who have already undergone HCT within the past 5 years
