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Recruiting NCT06945042

NCT06945042 ONC-LEUK-2406: The Impact of Systematic Financial Navigation in Acute Myeloid Leukemia

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Clinical Trial Summary
NCT ID NCT06945042
Status Recruiting
Phase
Sponsor Wake Forest University Health Sciences
Condition Acute Myeloid Leukemia
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-06-27
Primary Completion 2028-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 64 Years
Study Type INTERVENTIONAL
Interventions
Arm AArm B

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-06-27 with a primary completion date of 2028-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: 1. Ability to understand and willingness to sign an IRB-approved informed consent. 2. Age 18-64 years at the time of consent 3. Initial diagnosis of Acute Myeloid Leukemia (AML) per investigator Note: Date of initial diagnosis is the date of the bone marrow biopsy 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 30 days of therapy initiation 5. Ability to read and understand the English and/or Spanish language(s) 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. Exclusion Criteria: 1. Diagnosis of Acute Promyelocytic Leukemia 2. Unwilling to receive induction chemotherapy for AML 3. Previous treatment for hematologic malignancy 4. Prior allogeneic hematopoietic stem cell transplant

Contact & Investigator

Central Contact

Courtney Schepel

✉ Courtney.Schepel@advocatehealth.org

📞 (980) 442-2327

Principal Investigator

Thomas Knight, MD

PRINCIPAL INVESTIGATOR

Wake Forest University Health Sciences

Frequently Asked Questions

Who can join the NCT06945042 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 64 Years, studying Acute Myeloid Leukemia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06945042 currently recruiting?

Yes, NCT06945042 is actively recruiting participants. Contact the research team at Courtney.Schepel@advocatehealth.org for enrollment information.

Where is the NCT06945042 trial being conducted?

This trial is being conducted at Charlotte, United States, Winston-Salem, United States.

Who is sponsoring the NCT06945042 clinical trial?

NCT06945042 is sponsored by Wake Forest University Health Sciences. The principal investigator is Thomas Knight, MD at Wake Forest University Health Sciences. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology