RECRUITING

ONC-LEUK-2406: The Impact of Systematic Financial Navigation in Acute Myeloid Leukemia

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this research is to see how personal financial burden (financial toxicity) related to cancer affects the overall health and quality of life by evaluating the impact of systematic financial navigation in addition to standard financial distress interventions during cancer treatment.

Official Title

The Impact of Systematic Financial Navigation in Acute Myeloid Leukemia "SF-NAV"

Quick Facts

Study Start:2025-06-27
Study Completion:2028-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06945042

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 64 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Ability to understand and willingness to sign an IRB-approved informed consent.
  2. 2. Age 18-64 years at the time of consent
  3. 3. Initial diagnosis of Acute Myeloid Leukemia (AML) per investigator Note: Date of initial diagnosis is the date of the bone marrow biopsy
  4. 4. Planned intensive induction chemotherapy Note: It is acceptable if chemotherapy has been initiated at the time of enrollment as long as it is within 4 weeks of diagnosis
  5. 5. Ability to read and understand the English and/or Spanish language(s)
  6. 6. As determined by the enrolling investigator, ability of the participant to understand and comply with study procedures for the entire length of the study.
  1. 1. Diagnosis of Acute Promyelocytic Leukemia
  2. 2. Unwilling to receive induction chemotherapy for AML
  3. 3. Previous treatment for hematologic malignancy
  4. 4. Prior allogeneic hematopoietic stem cell transplant

Contacts and Locations

Study Contact

Courtney Schepel
CONTACT
(980) 442-2327
Courtney.Schepel@atriumhealth.org
Thomas Knight, MD
CONTACT
(980) 442-4363
Thomas.Knight@atriumhealth.org

Principal Investigator

Thomas Knight, MD
PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences

Study Locations (Sites)

Levine Cancer Insitute
Charlotte, North Carolina, 28204
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

  • Thomas Knight, MD, PRINCIPAL_INVESTIGATOR, Wake Forest University Health Sciences

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-27
Study Completion Date2028-05

Study Record Updates

Study Start Date2025-06-27
Study Completion Date2028-05

Terms related to this study

Keywords Provided by Researchers

  • Financial Navigation
  • Financial Toxicity

Additional Relevant MeSH Terms

  • Acute Myeloid Leukemia