Skip to content

Pilot Project on Interdisciplinary Therapy of Obesity

Pilot Project on Interdisciplinary Therapy of Obesity and Its Consequences on Body Weight, Quality of Life and Gastrointestinal Parameters

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01344525
Enrollment
480
Registered
2011-04-29
Start date
2009-05-31
Completion date
2029-05-31
Last updated
2018-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Weight Loss

Keywords

obesity therapy, metabolic syndrome, gastrointestinal tract, microbiota, metabolomics, micronutrients, outcome, sustainability

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.

Interventions

PROCEDURELaparoscopic gastric sleeve

Laparoscopic gastric sleeve

Gastric Banding

PROCEDUREMultidisciplinary lifstyle intervention

Multidisciplinary lifstyle intervention (OPTIFAST®52-program)

Roux-en-Y Bypass

Sponsors

German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
University of Hohenheim
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Body weight lossEvery 6 months for a period of 3 years

Secondary

MeasureTime frameDescription
Quality of lifeEvery 6 months for a period of 3 yearsSF-36, IWQOL-lite
Physical examinationEvery 6 months for a period of 3 yearsWeight, height, waist circumference, blood pressure, bioelectric impedance analysis, pulse etc.
Laboratory analysisEvery 6 months for a period of 3 yearsFasting glucose; Glutamat-Pyruvat- Transaminase (GPT); Lipid parameters (cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, triglycerides)
Vitamins/micronutrientsEvery 3-6 months for a period of maximal 3 yearsVitamin B1, B6, B12, ß-carotene, niacin, folic acid, selen and oxidative metabolites
Metabolomics, and Microflora analysisEvery 3-6 months for a period of maximal 3 years
Liver fatEvery 6 months for a period of 3 yearsLiver sonography
gut permeabilityEvery 6 months for a period of 3 yearsassessed by the uptake of inert molecules
peripheral blood lipopolysaccharide concentrationsEvery 6 months for a period of 3 years

Countries

Germany

Contacts

Primary ContactAntje Damms-Machado, Dipl. troph.
antje.machado@uni-hohenheim.de+49 711 451017707
Backup ContactKatrin Stingel, Dipl. troph.
k_stingel@uni-hohenheim.de+49 711 451017705

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026