Diet and Cognitive Training in Hematologic Cancer Survivors (NCT05708716)
A Multi-component Non-pharmacological Intervention to Improve Cognitive Outcomes in Hematologic Cancer Survivors
🩺 Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to examine feasibility of a cognitive intervention program in blood cancer survivors. The main questions it aims to answer are: * is it feasible to combine a ketogenic diet supplementation and online cognitive training in an intervention program * will patients using the combined intervention program have improved cognitive functioning compared to those who don't use it * how long will the intervention programs effects last Participants randomized to the intervention arm will consume an exogenous ketogenic supplementation and use an online cognitive training program for 12 weeks, while waitlist arm functions as a control group and will receive the online cognitive training only after a wait period of 12 weeks. Researchers will compare the intervention and waitlist control groups to see if the intervention improves cognitive functioning.
Who can join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham — Birmingham, Alabama
Age range: 21 Years
🧪 Interventions in This Study
- Modified ketogenic diet using an exogenous ketogenic formula (BEHAVIORAL)
- Online cognitive training (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of Alabama at Birmingham — Birmingham, Alabama
📞 Contact the Study Coordinator
Phone: (205) 638-2144
Email: nsharafeldin@uabmc.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Cognitive Impairment
- The Role of Large Artery Plaque Imaging Features in Predicting Inflammation and Cognition — Salt Lake City, Utah
- Cognitive Screening Made Easy for PCPs - R33 Phase — Austin, Texas
- Anticipating Decline and Providing Therapy — Winston-Salem, North Carolina
- Biomarkers for Vascular Contributions to Cognitive Impairment and Dementia Consortium — Los Angeles, California
- COgnitive and Physical Exercise to Improve Outcomes After Surgery (COPE-iOS) Study — Nashville, Tennessee
- The Care for America's Aging Study — Boston, Massachusetts
Explore by condition: All Cognitive Impairment clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.