Moffit Cancer Center
Tampa, Florida, 33612, United States
Location contact
Tiffany Carson, PhD
CONTACT
Tiffany Carson, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT03924778
The investigators will conduct a 2-arm randomized controlled pilot, feasibility feeding study in which 28 participants will be randomized to receive either a calorie-restricted Dietary Approaches to Stop Hypertension (DASH) diet or a calorie-restricted standard American diet provided by the study for 4 weeks. Participants will be non-Hispanic black or white, generally healthy females (14 black, 14 white). The investigators will collect fecal samples at multiple time points before, during, and after the dietary intervention to analyze for changes in the gut microbiota and functional-level metabolic products. This work will be led by an interdisciplinary team including expertise in bio-behavioral science, microbiology, nutrition science, bioinformatics, and biostatistics all with cross-cutting expertise in health disparities, prevention research, nutrition, the gut microbiota, inflammation and other biomarkers. The rationale for the proposed research is that once the interactions between race, diet, and the gut microbiota are more fully understood, targeted diet modifications may provide new and innovative approaches for the prevention and treatment of obesity and obesity-related diseases.
Trial opening soon.
Get Notified18 year and older
Female
Interventional
Not applicable
Tampa, Florida, 33612, United States
Tiffany Carson, PhD
CONTACT
Tiffany Carson, PhD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
brief description
describe
Time frame: Baseline to day 28
Weight change as measured by a scale in kilograms at multiple time points will be calculated and averaged.
Time frame: Day 28 to Day 42
Weight change as measured by a scale in kilograms at multiple time points will be calculated and averaged.
Time frame: Baseline to day 42
Weight change as measured by a scale in kilograms at multiple time points will be calculated and averaged.
Time frame: Baseline to day 28
The investigators will calculate changes in cholic acid in milligrams.
Time frame: day 28 to day 42
The investigators will calculate changes in cholic acid in milligrams.
Time frame: baseline to day 42
The investigators will calculate changes in cholic acid in milligrams.
Time frame: baseline to day 28
The investigators will calculate changes in c-reactive protein in mg/L.
Time frame: day 28 to day 42
The investigators will calculate changes in c-reactive protein in mg/L.
Time frame: baseline to day 42
The investigators will calculate changes in c-reactive protein in mg/L.
Time frame: baseline to day 28
The investigators will calculate changes in acetic acid in mmol/L
Time frame: day 28 to day 42
The investigators will calculate changes in acetic acid in mmol/L
Time frame: baseline to day 42
The investigators will calculate changes in acetic acid in mmol/L
Contact information is provided by the study sponsor or research team.
H. Lee Moffitt Cancer Center and Research Institute
Other
Modifying Diet and the Gut Microbiota to Reduce Obesity and Health Disparities
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07437976
Body Weight, Nutrition Disorders
Research Triangle Park, North Carolina, United States
View Trial DetailsNCT07478653
Body Weight, Dental Care for Children
Lexington, Kentucky, United States
View Trial DetailsNCT05713799
Body Weight, Glucose Metabolism Disorders
Bethesda, Maryland, United States
View Trial DetailsNCT07388537
Body Weight, Diabetes
Bethesda, Maryland, United States
View Trial Details