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Clinical Trials/NCT02855242
NCT02855242CompletedNot Applicable

Gut Microbiota Changes in Obese Individuals Undergoing Dedicated Lifestyle Modification Programs

Mayo Clinic1 site in 1 country32 target enrollmentStarted: April 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
32
Locations
1
Primary Endpoint
Changes in weight loss

Study Overview

Brief Summary

The human gut microbiota has become the subject of extensive research in recent years, particularly in regards to the role it plays in obesity. Although lifestyle factors, diet, and lack of exercise contribute largely to this obesity epidemic, there is increasing evidence that the human gut microbiota also influences weight gain.

The investigators hope to learn more information about the change in gut microbiota, especially with regards to those who are successful with weight loss, versus those who don't lose weight, after participating in a lifestyle modification program at the Dan Abraham Healthy Living Center (DAHLC).

Detailed Description

The gut microbiome is altered in obesity and is being increasingly studied given its role in energy harvest and fat storage with the hopeful goal of discovering a modifiable intervention to affect obesity and its consequences. Mouse models have already shown that transplantation of an obese microbiota into germ-free mice yields increased adiposity compared to transplantation of a lean microbiota. In humans, initial studies looked at the relative proportion of Bacteroidetes and Firmicutes in obese versus lean individuals and then followed those obese individuals who lost weight on low-calorie diets. The relative proportion of Bacteroidetes was decreased in obese people, and this then increased with weight loss. While certainly provocative, the findings were not consistently reproduced.

Subjects will include members of the Dan Abraham Healthy Living Center (DAHLC) program or the Healthy Living Program (HLP) at Mayo Clinic Rochester, who are seeking advice for weight management concerns.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Adults aged 18 and above;
  • •Subjects who are overweight or obese (BMI of 25 or greater);
  • •DAHLC/HLP eligible members who are able to access DAHLC support services;

Exclusion Criteria

  • •Known diagnosis of inflammatory bowel disease, microscopic colitis, celiac disease or other inflammatory conditions;
  • •Antibiotic use within the past 4 weeks (they can be enrolled after a four week washout period and subsequent use during the 6 month study duration does not exclude them);
  • •Bowel preparation for colonoscopy within the past week;
  • •Pregnancy or plans to become pregnant within the study time frame;
  • •Vulnerable Adults;
  • •Any other disease(s), condition(s) or habit(s) that would interfere with completion of the study, or in the judgment of the investigator would potentially interfere with compliance to this study or would adversely affect study outcomes;

Arms & Interventions

Intervention Program Group

Other

Lifestyle Counseling

Intervention: Lifestyle Counseling (Behavioral)

Controls Group

Active Comparator

No lifestyle counseling

Intervention: Controls Group (Other)

Outcomes

Primary Outcomes

Changes in weight loss

Time Frame: baseline to 6 months

enrolled in exercise program

Secondary Outcomes

  • Changes in gut microbiota(Baseline to 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Purna C. Kashyap, MBBS

PI

Mayo Clinic

Study Sites (1)

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