UF-BMT-HSCT-001: A Non-Interventional Study Evaluating Diet in HSCT Survivors



Status:Recruiting
Healthy:No
Age Range:18 - 99
Updated:1/2/2019
Start Date:December 14, 2017
End Date:January 2022
Contact:Lacey Mead
Email:lem23@ufl.edu
Phone:(352) 224-7049

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UF-BMT-HSCT-001: A Non-Interventional Study Evaluating the Quality of Diet in Allogeneic and Autologous Hematopoietic Stem Cell Transplant Survivors

This is a single center, cross-sectional, non-interventional study aimed at the nutritional
intake of long-term health of allogeneic or autologous hematopoietic stem cell transplant
(HSCT) survivors.

Higher rates of comorbidity among hematopoietic stem cell transplant (HSCT) survivors support
the need for lifestyle interventions that target this vulnerable population. Comprehensive
evaluation of the nutrient intake will provide adequate information necessary for develop of
a targeted nutritional intervention in order to achieve specific nutritional need and improve
long-term health of HSCT survivors. The cross-sectional design of this study has been
selected for the timely collection of subject reported nutrient intake data. The intended
study is strictly observational.

Inclusion Criteria:

- Written informed consent obtained from the subject and the ability for the subject to
comply with all the study-related procedures for subjects enrolled from the cancer
registry.

- Both males and females ≥ 18 years of age.

- A medical history of allogeneic or autologous hematopoietic stem cell transplant
(HSCT), irrespective of the disease. For the purpose of this study, HSCT survivor is
defined as subjects one or more years after allogeneic or autologous HSCT without
disease relapse, active graft-versus-host disease, or active infection. Subjects with
chronic graft versus host disease who are on stable dose of immunosuppressant (or
being tapered off of immunosuppressant) over the past 3 months will be eligible.

- Study participants must have the ability to complete the questionnaires through one of
the previously stated mechanisms.

- English speaking due to the logistics of the questionnaires and phone contact included
in this study.

Exclusion Criteria:

- Subjects demonstrating an inability to comply with the study procedures.
We found this trial at
1
site
Gainesville, Florida 32610
Principal Investigator: Nosha Farhadfar, MD
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mi
from
Gainesville, FL
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