Actively Recruiting
Intervention for Fatigue in HCT Recipients
Led by Massachusetts General Hospital · Updated on 2024-12-11
66
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
N
National Heart, Lung, and Blood Institute (NHLBI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to assess whether a cognitive-behavioral therapy (CBT) for fatigue intervention is acceptable, feasible, and effective at managing fatigue and improving quality of life for patients following hematopoietic stem cell transplant (HCT).
CONDITIONS
Official Title
Intervention for Fatigue in HCT Recipients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients 18 years or older
- Ability to speak and read English
- Underwent autologous or allogeneic transplant more than 6 months before enrollment
- No evidence of disease relapse requiring therapy
- No new malignancy requiring therapy after transplant
- Report moderate to severe fatigue in the past week (rating 4 or higher on a 0-10 scale)
- Currently receiving care at the MGH Blood and Marrow Transplant Clinic
You will not qualify if you...
- Active cognitive impairment or uncontrolled psychiatric illness such as schizophrenia that prevents informed consent or participation
- Currently receiving cognitive-behavioral therapy care
- Living with untreated sleep apnea
- Having hypoxemia requiring oxygen supplementation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Massachusetts General Hospital Cancer Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
Research Team
A
Ashley Nelson, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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