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Financial Navigation for Blood Cancer Survivors
N/A
Waitlist Available
Led By Susan K Parsons, MD, MRP
Research Sponsored by Tufts Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial studies how young adult cancer survivors (18-39y) experience financial strain and seeks to find ways to help.
Who is the study for?
This trial is for young adults aged 18-39 in the U.S. who were diagnosed with blood cancer (like leukemia or lymphoma) during childhood or early adulthood, are off treatment or on a stable regimen, and have been living with their diagnosis for at least three years. They must read English and not be dependent on a parent's insurance.
What is being tested?
The study tests financial navigation services to address money-related stress in young adult blood cancer survivors. Participants will receive different levels of support: active guidance, occasional help, or no special assistance from the study to manage financial challenges.
What are the potential side effects?
Since this trial focuses on financial counseling rather than medical intervention, there are no direct physical side effects expected from participating in the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Personal Financial Wellness Scale (PFW)
Secondary study objectives
Health-Related Quality of Life (HrQoL) Measures
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Active Control
Group I: Active NavigationActive Control1 Intervention
Active navigation with the study-based financial navigator scheduling four check-in meetings throughout the study with the participant. All participants will complete an assessment at baseline, 3 months and 6 months and be invited to participate in an optional interview after the 6-month assessment.
Group II: Ad Hoc NavigationActive Control1 Intervention
Ad hoc navigation in which participant is provided study-based financial navigator to contact as needed. All participants will complete an assessment at baseline, 3 months and 6 months and be invited to participate in an optional interview after the 6-month assessment.
Group III: No study-based NavigationActive Control1 Intervention
No access to a study-based financial navigator, but access to a national hotline through the Leukemia \& Lymphoma Society. All participants will complete an assessment at baseline, 3 months and 6 months and be invited to participate in an optional interview after the 6-month assessment.
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Who is running the clinical trial?
Tufts Medical CenterLead Sponsor
263 Previous Clinical Trials
264,208 Total Patients Enrolled
The Leukemia and Lymphoma SocietyOTHER
85 Previous Clinical Trials
26,034 Total Patients Enrolled
Susan K Parsons, MD, MRPPrincipal InvestigatorTufts Medical Center
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 18 and 39 years old.I am either not on treatment for blood cancer or taking oral medication with my disease stable.I have been diagnosed and treated for a type of blood cancer before.I am covered under my parent or guardian's insurance.I am either not currently receiving treatment for a second type of cancer or am on a stable, long-term treatment plan.I was diagnosed with blood cancer over three years ago.I was diagnosed with blood cancer between the ages of 0 and 36.
Research Study Groups:
This trial has the following groups:- Group 1: Active Navigation
- Group 2: Ad Hoc Navigation
- Group 3: No study-based Navigation
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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