- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05372445
Microbiome and Health Indicators in People With Obesity, Prediabetes and Type 2 Diabetes Undergoing a Lifestyle Intervention (MicrobiAr)
MicrobiAr: Characterization and Follow-up of Microbiome and Health Indicators in Obese, Pre-Diabetes and Type 2 Diabetes Cohorts Undergoing a Plant-based Diet and Lifestyle Intervention
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The present study has 2 stages, one cross-sectional and the other longitudinal. In the cross-sectional stage, a characterization of a single sampling of 480 people divided into 4 cohorts of 120 people each will be carried out: reference controls, subjects with obesity, with prediabetes and with type 2 diabetes. A clinical history will be made, as long as a 7-day food record and clinical laboratory tests. Anthropometric assessment will be carried out by recording weight, height, waist and hip circumference, determination of waist/hip ratios, as well as taking 4 skinfolds, bicipital, triceps, subscapular and suprailiac, arm and calf measurements and force through a dynamometer. The 480 people will also undergo gut microbiota and microbiome tests from stool samples.
During the longitudinal stage, subjects of each cohort (120 with obesity, 120 with prediabetes and 120 with type 2 diabetes) will be randomly divided into two intervention groups (with 60 subjects each). One group will follow a non-intensive intervention (personalized face-to-face follow-up every 2 months). The other group will follow an intensive intervention (personalized face-to-face follow-up every 3 weeks and a weekly remote group meeting). In both cases, a food plan will be followed based on the recommendations of the nutrition service of the Hospital de Clínicas, Argentina, in accordance with recommendations from the American Diabetes Association (ADA) 2019 guidelines with an emphasis on plant-based diet and whole foods.
Follow-up and nutritional guidance
Groups of 15 subjects from each intervention arm will be led by 3 healthcare professionals. In every case, the group's functions will be:
- Obtain a unique 7 day food-recall from all subjects, and upload the data to "MAR24" platform (for the transversal stage).
- Obtain a 2 day food-recall (including one day from the weekend) from all subjects every two months, and upload the data to "MAR24" platform (for the longitudinal stage).
- Complete a shared spreadsheet with clinical, biochemical and anthropometric parameters of every subject's visits to the hospital.
- Collaborate in Whatsapp unidirectional groups. In the non-intensive arm, the messages will only be to remember patients about their visits to the hospital, while in the intensive arm it will also be about other activities, such as workshops.
- Detect subjects who miss their appointments, to establish personalized contact and apply motivational strategies in order to reduce dropout risk.
To accomplish the mentioned tasks, the group leaders will have support from several students from nutrition careers and healthcare professionals.
Influence of physical activity and exercise
A structured physical exercise protocol will be delivered to all subjects. This protocol includes a warm-up, 3 series of 1 minute of eight different strength exercises, with 2 a minute rest. The objective is to accomplish three sessions per week, which can be done in person and supervised by specialists in the Hospital, or online via video call. Subjects will have to record the amount of achieved repetitions in each series of every exercise already done by each session.
The training volume will be adapted according to the subject's capabilities and progress, with the objective of increasing the number of series and reducing resting time between exercises.
Specific follow-up and support proposals for the intensive intervention
In addition to the already mentioned tasks in the follow-up and nutritional guidance's section, for the intensive intervention subjects, group's functions will also be:
- Collaborate in the assembly and execution of virtual food education workshops;
- Coordinate weekly meetings with the 15 assigned subjects, where adherence should be encouraged during the first 3 months. Then, meetings will be spaced out at a minimum of 15 days to 30 days;
- Contribute to the planning of various activities that seek to maximize adherence to the clinical trial of the entire intensive intervention group;
- Coordinate face-to-face visits for nutritional support every 3 weeks for each subject;
- Monitoring adherence through 48-hour records (1 day a week and 1 day a weekend) using the MAR24 platform. Data will be collected by phone calls or video calls to each subject with a frequency of 1 call per month.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Juan Bustamante, PhD
- Phone Number: +541164419444
- Email: bustamante.bio@gmail.com
Study Contact Backup
- Name: Gustavo Frechtel, PhD
- Phone Number: +541154066193
- Email: gfrechtel@yahoo.com
Study Locations
-
-
Buenos Aires
-
Capital Federal, Buenos Aires, Argentina, C1120AAR
- Recruiting
- Hospital de Clinicas "Jose De San Martin"
-
Contact:
- Gustavo Frechtel, Doctor, PhD
- Phone Number: +54 9 11 54066193
- Email: gfrechtel@yahoo.com
-
Contact:
- Juan Bustamante, PhD
- Phone Number: +54 9 11 64419444
- Email: bustamante.bio@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria for control or reference group:
- Subjects without type 2 diabetes, obesity, prediabetes (glucose intolerance), or metabolic syndrome
- HbA1c less than 42mmol/mol (<5.7%)
- BMI between 18.5 and 24.9
Inclusion Criteria for people with obesity:
- BMI greater than 30
Inclusion Criteria for people with prediabetes:
- Fasting glucose between 110 and 125 mg/dl
- HbA1c between 42 and 47 mmol/mol (5.7% to 6.4%)
- BMI greater than 30
Inclusion Criteria for people with type 2 diabetes:
- Fasting glucose > 126 mg/dl
- HbA1c > 48mmol/mol (6.5% or higher)
- BMI greater than 30
- Treatment with metformin at therapeutic dose (1500-2000 mg/day) or maximum tolerated dose.
Exclusion Criteria:
- Subjects with obesity, pre-diabetes medicated with metformin or another drug for diabetes or obesity
- Subjects with type 2 diabetes medicated with another drug that is not metformin
- Subjects with type 2 diabetes diagnosed over 6 years
- Subjects with type 2 diabetes requiring insulin
- Chronic kidney disease grade greater than 3 (measured by EPI)
- Subjects with type 1 diabetes
- Intestinal diseases, Crohn's, ulcerative colitis, celiac disease
- Use of antibiotics in the last 3 months
- Pregnancy, lactation
- Psychiatric disorders
- Eating disorder
- Gastric bypass surgery
- Transplanted people
- Oncological pathology diagnosed less than 5 years
- Subjects who do not wish to sign the informed consent
- Subjects who do not agree to participate in the study over the 2 years follow-up
- Subjects who do not have electronic devices and the internet to hold virtual meetings
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Reference Group
People between 30-60 years old, without obesity, prediabetes or type 2 diabetes. The purpose of this group is to characterize gut microbiota and microbiome to set the reference values of the argentinian local population. |
|
Active Comparator: Obesity Group A
People between 30-60 years old, diagnosed with obesity assigned to the non-intensive intervention.
|
After an evaluation of 7 day initial food-recall, subjects will receive counseling in order to improve their dietary habits, according to the American Diabetes Association 2019 Guidelines. The goals of this intervention are (i) achieve a caloric restriction of 500 kcal from their habitual energy intake, (ii) prioritize natural, minimally processed foods with a low glycemic index and glycemic load, (iii) eat lean protein sources, both from plant and animal origin and (iv) gradual increments of fiber intake, to achieve at least the minimum recommendations for the general population. The frequency of the follow-up appointments will be every 4 weeks, alternating between a clinical control and nutritional one. Therefore, the planned nutritional follow-up frequency will be every 2 months. In these appointments, the objective will be to achieve the mentioned energy intake reduction of 500 kcal, aiming to the nutritional goals previously mentioned, with the aid of the food-recalls.
Other Names:
|
Experimental: Obesity Group B
People between 30-60 years old, diagnosed with obesity assigned to the intensive intervention.
|
People will have virtual education with food and nutrition coaching workshops, as well as weekly meetings in small groups as a support and follow-up groups. The frequency of the face-to-face follow-up appointments will be every 3 weeks. The nutritional intervention will emphasize the consumption of mainly minimally processed food from plant origin. A vitamin b12 supplement per week will be provided. This intervention group will have 2 stages. First stage will have a duration of 3 months setting the nutritional bases going to a plant-based diet with basic considerations regarding fiber intake reducing meat consumption, and incorporating protein from vegetable sources, among other considerations. Second stage will progress to higher levels of fiber and others nutritional requeriments in order to intensify the nutritional plant-based intervention.
Other Names:
|
Active Comparator: Prediabetes Group A
People between 30-60 years old, diagnosed with prediabetes assigned to the non-intensive intervention.
|
After an evaluation of 7 day initial food-recall, subjects will receive counseling in order to improve their dietary habits, according to the American Diabetes Association 2019 Guidelines. The goals of this intervention are (i) achieve a caloric restriction of 500 kcal from their habitual energy intake, (ii) prioritize natural, minimally processed foods with a low glycemic index and glycemic load, (iii) eat lean protein sources, both from plant and animal origin and (iv) gradual increments of fiber intake, to achieve at least the minimum recommendations for the general population. The frequency of the follow-up appointments will be every 4 weeks, alternating between a clinical control and nutritional one. Therefore, the planned nutritional follow-up frequency will be every 2 months. In these appointments, the objective will be to achieve the mentioned energy intake reduction of 500 kcal, aiming to the nutritional goals previously mentioned, with the aid of the food-recalls.
Other Names:
|
Experimental: Prediabetes Group B
People between 30-60 years old, diagnosed with prediabetes assigned to the intensive intervention.
|
People will have virtual education with food and nutrition coaching workshops, as well as weekly meetings in small groups as a support and follow-up groups. The frequency of the face-to-face follow-up appointments will be every 3 weeks. The nutritional intervention will emphasize the consumption of mainly minimally processed food from plant origin. A vitamin b12 supplement per week will be provided. This intervention group will have 2 stages. First stage will have a duration of 3 months setting the nutritional bases going to a plant-based diet with basic considerations regarding fiber intake reducing meat consumption, and incorporating protein from vegetable sources, among other considerations. Second stage will progress to higher levels of fiber and others nutritional requeriments in order to intensify the nutritional plant-based intervention.
Other Names:
|
Active Comparator: Type 2 Diabetes Group A
People between 30-60 years old, diagnosed with type 2 diabetes assigned to the non-intensive intervention.
|
After an evaluation of 7 day initial food-recall, subjects will receive counseling in order to improve their dietary habits, according to the American Diabetes Association 2019 Guidelines. The goals of this intervention are (i) achieve a caloric restriction of 500 kcal from their habitual energy intake, (ii) prioritize natural, minimally processed foods with a low glycemic index and glycemic load, (iii) eat lean protein sources, both from plant and animal origin and (iv) gradual increments of fiber intake, to achieve at least the minimum recommendations for the general population. The frequency of the follow-up appointments will be every 4 weeks, alternating between a clinical control and nutritional one. Therefore, the planned nutritional follow-up frequency will be every 2 months. In these appointments, the objective will be to achieve the mentioned energy intake reduction of 500 kcal, aiming to the nutritional goals previously mentioned, with the aid of the food-recalls.
Other Names:
|
Experimental: Type 2 Diabetes Group B
People between 30-60 years old, diagnosed with type 2 diabetes assigned to the intensive intervention.
|
People will have virtual education with food and nutrition coaching workshops, as well as weekly meetings in small groups as a support and follow-up groups. The frequency of the face-to-face follow-up appointments will be every 3 weeks. The nutritional intervention will emphasize the consumption of mainly minimally processed food from plant origin. A vitamin b12 supplement per week will be provided. This intervention group will have 2 stages. First stage will have a duration of 3 months setting the nutritional bases going to a plant-based diet with basic considerations regarding fiber intake reducing meat consumption, and incorporating protein from vegetable sources, among other considerations. Second stage will progress to higher levels of fiber and others nutritional requeriments in order to intensify the nutritional plant-based intervention.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical improvements in people with type 2 diabetes, prediabetes, or obesity
Time Frame: at 2 years, checked every 6 months
|
These clinical improvements will be defined as:
Any of the three possible situations will be considered as a clinical improvement event. |
at 2 years, checked every 6 months
|
Gut microbiota metabolic pathways changes
Time Frame: at 2 years, checked every 6 months
|
Increase in the number of gut microbiota metabolic pathways possibly expressed in subjects of intensive intervention compared to their baseline states and also compared to subjects of the non-intensive intervention.
This metric refers to possibly expressed metabolic pathways predicted from shotgun metagenomics analysis related to regulation of inflammatory processes, carcinogenesis, intestinal barrier function, oxidative stress, production of SCFAs, regulation of immune response and inflammation, production of derivative aromatic amino acids, regulation of bile acids (synthesis of derivative metabolites of cholesterol), regulation of the level of phospholipid synthesis (anaerobic metabolism of choline).
|
at 2 years, checked every 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Metabolic syndrome regression
Time Frame: at 2 years, checked every 6 months
|
Participants with diagnosis of metabolic syndrome at baseline who no longer meet metabolic syndrome criteria, according to those established by the Joint Interim Statement in 2009 (Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity.
Circulation.
2009;120:1640 -1645.)
|
at 2 years, checked every 6 months
|
Insulin resistance
Time Frame: at 2 years
|
Measured by HOMA-IR, HOMA-B or triglyceride: HDL-C ratio.
|
at 2 years
|
Gut microbiota diversity changes
Time Frame: at 2 years, checked every 6 months
|
Increase of diversity in gut microbiota observed in subjects of the intensive intervention compared to subjects of the non-intensive intervention and also compared to their baseline states.
|
at 2 years, checked every 6 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Juan Bustamante, PhD, CONICET Researcher
- Principal Investigator: Gustavo Frechtel, PhD, CONICET Researcher
Publications and helpful links
General Publications
- Alberti KG, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, Fruchart JC, James WP, Loria CM, Smith SC Jr; International Diabetes Federation Task Force on Epidemiology and Prevention; Hational Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; International Association for the Study of Obesity. Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009 Oct 20;120(16):1640-5. doi: 10.1161/CIRCULATIONAHA.109.192644. Epub 2009 Oct 5.
- Riddle MC, Cefalu WT, Evans PH, Gerstein HC, Nauck MA, Oh WK, Rothberg AE, le Roux CW, Rubino F, Schauer P, Taylor R, Twenefour D. Consensus Report: Definition and Interpretation of Remission in Type 2 Diabetes. Diabetes Care. 2021 Aug 30;44(10):2438-44. doi: 10.2337/dci21-0034. Online ahead of print.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MicrobiAr
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Obesity
-
Central Hospital, Nancy, FranceNot yet recruiting
-
University of MinnesotaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Active, not recruitingAdolescent ObesityUnited States
-
Helsinki University Central HospitalKarolinska Institutet; Folkhälsan Researech CenterEnrolling by invitation
-
Istanbul Medipol University HospitalMedipol UniversityCompletedObesity, Morbid | Obesity, Adolescent | Obesity, Abdominal | Weight, Body | Obesity, VisceralTurkey
-
Queen Fabiola Children's University HospitalNot yet recruitingMorbid Obesity | Adolescent Obesity | Bariatric SurgeryBelgium
-
Azienda Ospedaliero-Universitaria Consorziale Policlinico...Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies; Istituti... and other collaboratorsCompletedMorbid Obesity | Metabolically Healthy ObesityItaly
-
Washington University School of MedicinePatient-Centered Outcomes Research Institute; Pennington Biomedical Research... and other collaboratorsActive, not recruitingOvernutrition | Nutrition Disorders | Overweight | Body Weight | Pediatric Obesity | Body Weight Changes | Childhood Obesity | Weight Gain | Adolescent Obesity | Obesity, Childhood | Overweight and Obesity | Overweight or Obesity | Overweight AdolescentsUnited States
-
The Hospital for Sick ChildrenCompleted
-
Ihuoma EneliCompletedObesity, ChildhoodUnited States
-
Fundació Sant Joan de DéuRecruitingObesity, Childhood | Obesity, AdolescentSpain
Clinical Trials on Non-intensive intervention
-
University of South CarolinaUniversidad de Costa Rica; Municipality of Alajuela; Agenda de MujeresCompleted
-
Adaliene Versiani M. FerreiraConselho Nacional de Desenvolvimento Científico e Tecnológico; Fundacion MAPFRERecruiting
-
NYU Langone HealthCompletedHypertension | Hypertensive Heart DiseaseUnited States
-
The University of Hong KongSuspendedInsomnia | PreDiabetes | Sleep DeprivationHong Kong
-
Northwestern UniversitySarah M. Friedewald, MD; Jennifer N. Choi, MDCompleted
-
Riphah International UniversityCompleted
-
Emory UniversityNational Institute on Minority Health and Health Disparities (NIMHD)CompletedEnd-stage Renal Disease
-
Second Affiliated Hospital, School of Medicine,...Recruiting
-
The Miriam HospitalNational Institute of Mental Health (NIMH); University of Rochester; Syracuse...CompletedHIV Infections | Sexually Transmitted DiseasesUnited States
-
University of ZurichUnknownAutism Spectrum DisorderSwitzerland