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RECRUITING
NCT05708716
NA

Diet and Cognitive Training in Hematologic Cancer Survivors

Sponsor: University of Alabama at Birmingham

View on ClinicalTrials.gov

Summary

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.

Official title: A Multi-component Non-pharmacological Intervention to Improve Cognitive Outcomes in Hematologic Cancer Survivors

Key Details

Gender

All

Age Range

21 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2022-11-22

Completion Date

2027-04-30

Last Updated

2025-12-17

Healthy Volunteers

No

Interventions

BEHAVIORAL

Modified ketogenic diet using an exogenous ketogenic formula

Participants will follow a modified ketogenic diet consuming a daily exogenous ketogenic meal replacement formula while limiting their carbohydrate intake for 12 weeks.

BEHAVIORAL

Online cognitive training

Participants will complete a daily session of 5 online cognitive training tasks for 12 weeks.

Locations (1)

University of Alabama at Birmingham

Birmingham, Alabama, United States