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Pilot Project on Interdisciplinary Therapy of Obesity

Primary Purpose

Obesity, Weight Loss

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Laparoscopic gastric sleeve
Gastric Banding
Multidisciplinary lifstyle intervention
Roux-en-Y Bypass
Sponsored by
University of Hohenheim
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring obesity therapy, metabolic syndrome, gastrointestinal tract, microbiota, metabolomics, micronutrients, outcome, sustainability

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults (18-65 years at time of inclusion)
  • Obesity defined as BMI > 30 kg/m2
  • Obesity treatment (multidisciplinary life style intervention with LCD or bariatric surgery) resulting in an estimated body weight loss of >10% of the initial body weight within 6 month

Exclusion Criteria:

  • Body weight loss after intervention < 10%
  • Follow-up period < 1 year or number of consultations within 3 years < 3

Sites / Locations

  • University of HeidelbergRecruiting
  • University of HohenheimRecruiting
  • University of TübingenRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Experimental

Experimental

Experimental

Arm Label

Control group

"low-calorie-diet (LCD)"-based lifestyle intervention

Laparoscopic gastric sleeve intervention

Conventional bariatric surgery

Arm Description

Nutritional counselings every 6 months, no further intervention

12 months multidisciplinary weight loss program including three months low-calorie formula diet (800 kcal) (OPTIFAST®52 program)

Gastric Banding and Gastric Bypass

Outcomes

Primary Outcome Measures

Body weight loss

Secondary Outcome Measures

Quality of life
SF-36, IWQOL-lite
Physical examination
Weight, height, waist circumference, blood pressure, bioelectric impedance analysis, pulse etc.
Laboratory analysis
Fasting glucose; Glutamat-Pyruvat- Transaminase (GPT); Lipid parameters (cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, triglycerides)
Vitamins/micronutrients
Vitamin B1, B6, B12, ß-carotene, niacin, folic acid, selen and oxidative metabolites
Metabolomics, and Microflora analysis
Liver fat
Liver sonography
gut permeability
assessed by the uptake of inert molecules
peripheral blood lipopolysaccharide concentrations

Full Information

First Posted
April 27, 2011
Last Updated
October 25, 2018
Sponsor
University of Hohenheim
Collaborators
German Federal Ministry of Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT01344525
Brief Title
Pilot Project on Interdisciplinary Therapy of Obesity
Official Title
Pilot Project on Interdisciplinary Therapy of Obesity and Its Consequences on Body Weight, Quality of Life and Gastrointestinal Parameters
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Recruiting
Study Start Date
May 2009 (undefined)
Primary Completion Date
May 2029 (Anticipated)
Study Completion Date
May 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Hohenheim
Collaborators
German Federal Ministry of Education and Research

4. Oversight

5. Study Description

Brief Summary
Obese individuals that undergo major intervention such as a low-calorie formula diet program or bariatric surgery with the result of substantial weight loss (> 10%) are included and followed-up for at least 3 years. Weight changes and excess weight loss as well as measures of quality of life are monitored. In addition, biomaterials will be collected from these individuals every 6 months for measurement of parameters related to obesity-associated gastrointestinal (GI) impairments such as change in GI hormone levels, change in GI microbiota, or enhanced bacterial translocation. Moreover, micronutrient and metabolomics analysis will be performed. This project allows comparison of non-surgical and surgical intervention and enables to asses the anticipated relationship between obesity and the GI tract in humans in the future.
Detailed Description
A database and a biomaterial bank will be established to assess, if the role of the gut for the development of obesity and obesity-related diseases such as fatty liver are of relevance in humans, e.g. for classification of afflicted individuals regarding risk or outcome after intervention. During 3 years, the investigators will include 480 obese individuals (4 cohorts of 120 individuals) who undergo a treatment program (either surgical or non-surgical), and follow them up for at least 3 years. Every 6 months, a visit is planned at the obesity center where the initial intervention has been performed. Within the visits, anthropometry (Body Mass Index (BMI), excess body weight (EBW), bioelectrical impedance analysis (BIA)), quality of life (SF36 score, Impact Of Weight On Quality Of Life (IWQOL) questionnaire), and sample collection for laboratory analyses (inflammatory markers, hormones, flora composition, micronutrients, metabolomics etc.) will be performed. Patients will be recruited from 3 centers in Germany. The long-term expectation from this model project is to find gastrointestinal parameters allowing to predict outcome and sustainability of different intervention strategies. In addition, intervention programs will be compared regarding long-term outcome and quality of life changes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Weight Loss
Keywords
obesity therapy, metabolic syndrome, gastrointestinal tract, microbiota, metabolomics, micronutrients, outcome, sustainability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
480 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
No Intervention
Arm Description
Nutritional counselings every 6 months, no further intervention
Arm Title
"low-calorie-diet (LCD)"-based lifestyle intervention
Arm Type
Experimental
Arm Description
12 months multidisciplinary weight loss program including three months low-calorie formula diet (800 kcal) (OPTIFAST®52 program)
Arm Title
Laparoscopic gastric sleeve intervention
Arm Type
Experimental
Arm Title
Conventional bariatric surgery
Arm Type
Experimental
Arm Description
Gastric Banding and Gastric Bypass
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic gastric sleeve
Intervention Description
Laparoscopic gastric sleeve
Intervention Type
Procedure
Intervention Name(s)
Gastric Banding
Intervention Description
Gastric Banding
Intervention Type
Procedure
Intervention Name(s)
Multidisciplinary lifstyle intervention
Intervention Description
Multidisciplinary lifstyle intervention (OPTIFAST®52-program)
Intervention Type
Procedure
Intervention Name(s)
Roux-en-Y Bypass
Intervention Description
Roux-en-Y Bypass
Primary Outcome Measure Information:
Title
Body weight loss
Time Frame
Every 6 months for a period of 3 years
Secondary Outcome Measure Information:
Title
Quality of life
Description
SF-36, IWQOL-lite
Time Frame
Every 6 months for a period of 3 years
Title
Physical examination
Description
Weight, height, waist circumference, blood pressure, bioelectric impedance analysis, pulse etc.
Time Frame
Every 6 months for a period of 3 years
Title
Laboratory analysis
Description
Fasting glucose; Glutamat-Pyruvat- Transaminase (GPT); Lipid parameters (cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, triglycerides)
Time Frame
Every 6 months for a period of 3 years
Title
Vitamins/micronutrients
Description
Vitamin B1, B6, B12, ß-carotene, niacin, folic acid, selen and oxidative metabolites
Time Frame
Every 3-6 months for a period of maximal 3 years
Title
Metabolomics, and Microflora analysis
Time Frame
Every 3-6 months for a period of maximal 3 years
Title
Liver fat
Description
Liver sonography
Time Frame
Every 6 months for a period of 3 years
Title
gut permeability
Description
assessed by the uptake of inert molecules
Time Frame
Every 6 months for a period of 3 years
Title
peripheral blood lipopolysaccharide concentrations
Time Frame
Every 6 months for a period of 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (18-65 years at time of inclusion) Obesity defined as BMI > 30 kg/m2 Obesity treatment (multidisciplinary life style intervention with LCD or bariatric surgery) resulting in an estimated body weight loss of >10% of the initial body weight within 6 month Exclusion Criteria: Body weight loss after intervention < 10% Follow-up period < 1 year or number of consultations within 3 years < 3
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antje Damms-Machado, Dipl. troph.
Phone
+49 711 451017707
Email
antje.machado@uni-hohenheim.de
First Name & Middle Initial & Last Name or Official Title & Degree
Katrin Stingel, Dipl. troph.
Phone
+49 711 451017705
Email
k_stingel@uni-hohenheim.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan C. Bischoff, Prof. Dr.
Organizational Affiliation
University of Hohenheim, Institute of Nutritional Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Heidelberg
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Name
University of Hohenheim
City
Stuttgart
ZIP/Postal Code
70599
Country
Germany
Individual Site Status
Recruiting
Facility Name
University of Tübingen
City
Tübingen
ZIP/Postal Code
72076
Country
Germany
Individual Site Status
Recruiting

12. IPD Sharing Statement

Citations:
PubMed Identifier
28049662
Citation
Damms-Machado A, Louis S, Schnitzer A, Volynets V, Rings A, Basrai M, Bischoff SC. Gut permeability is related to body weight, fatty liver disease, and insulin resistance in obese individuals undergoing weight reduction. Am J Clin Nutr. 2017 Jan;105(1):127-135. doi: 10.3945/ajcn.116.131110. Epub 2016 Nov 9.
Results Reference
derived
PubMed Identifier
25710027
Citation
Damms-Machado A, Mitra S, Schollenberger AE, Kramer KM, Meile T, Konigsrainer A, Huson DH, Bischoff SC. Effects of surgical and dietary weight loss therapy for obesity on gut microbiota composition and nutrient absorption. Biomed Res Int. 2015;2015:806248. doi: 10.1155/2015/806248. Epub 2015 Feb 1.
Results Reference
derived
PubMed Identifier
22657586
Citation
Damms-Machado A, Weser G, Bischoff SC. Micronutrient deficiency in obese subjects undergoing low calorie diet. Nutr J. 2012 Jun 1;11:34. doi: 10.1186/1475-2891-11-34.
Results Reference
derived
PubMed Identifier
22403000
Citation
Damms-Machado A, Friedrich A, Kramer KM, Stingel K, Meile T, Kuper MA, Konigsrainer A, Bischoff SC. Pre- and postoperative nutritional deficiencies in obese patients undergoing laparoscopic sleeve gastrectomy. Obes Surg. 2012 Jun;22(6):881-9. doi: 10.1007/s11695-012-0609-0.
Results Reference
derived

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Pilot Project on Interdisciplinary Therapy of Obesity

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