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BagEL - Bariatric Patients in Primary Care: Post-operative Nutrition and Lifestyle Management

BagEL - Bariatric Patients in Primary Care: Post-operative Nutrition and Lifestyle Management Evaluation of a Post-operative Nutrition and Lifestyle Management for Lifelong Care of Post-bariatric Patients in Primary Care

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03792412
Enrollment
220
Registered
2019-01-03
Start date
2018-05-22
Completion date
2020-01-31
Last updated
2019-01-03

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

Conditions

Bariatric Surgery Candidate, Malnutrition

Keywords

bariatric surgery, lifelong follow-up, primary care, obesity, health care study

Brief summary

There is a growing number of patients undergoing bariatric surgery requiring lifelong follow-up. BagEL (Bariatric Patients in Primary Care: Post-operative Nutrition and Lifestyle Management) is a survey to evaluate a newly developed structured disease management program including nutrition and lifestyle management in primary care.

Detailed description

During last decades the prevalence of obesity is growing. Therefore, the number of bariatric procedures are also increasing. Frequent complications after surgery are nutritional deficiencies (e.g. vitamins, minerals, protein) which require mandatory long-term follow-up. So far adequate follow-up programs are only provided in specialized bariatric centers like in the outpatient clinic for obesity at the General Hospital of Vienna. These programs are focusing on prevention and premature identification of deficiencies. Rising numbers of bariatric-surgical procedures pose a challenge for bariatric centres because of the accumulating numbers of bariatric patients requesting follow-up at least once a year. To provide full coverage an appropriate possibility would be to transfer follow up to non-specialised facilities including general practitioners and family doctors using a so called pass providing practical treatment recommendations (necessary follow-up appointments, laboratory blood tests, questions regarding nutrition and lifestyle behavior). To our best knowledge such a structured post-bariatric care management program in primary care does not exist by now. The aim of this study is therefore the evaluation of such a pass.

Interventions

Patients receive the usability questionnaire and a structured nutrition and lifestyle program for post-bariatric follow-up visits. Twice in six months the patients visit their family doctor and hand over the usability questionnaire to evaluate the structured follow-up program for postbariatric patients. Family doctors fill out the questionnaire and returns it to the investigator.

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

pseudonymity

Intervention model description

randomised cohort study with control group

Eligibility

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

Inclusion criteria

* older than 18 years and each sex, * bariatric-surgical treatment - in particular omega loop gastric bypass, Roux-en-Y-gastric bypass - and sleeve gastrectomy at the department of surgery General Hospital Vienna, * Operation date maximum 21 months before study beginning,

Exclusion criteria

* Pregnancy (a possible existing pregnancy is excluded by questioning) * Nursing mothers * Not German speaking patients

Design outcomes

Primary

MeasureTime frameDescription
Usability questionnaire6 monthsUsability of the follow-up passes (intervention and control) will be evaluated in primary care. In a pilot study the usability questionnaire was evaluated. The patient hands over the follow-up pass together with the questionnaire at each appointment (twice) at the family doctor. A stamped envelope to return the questionnaire is included. Family doctors will be asked to complete a series of actions regarding the content of the follow-up passes. Each action will be rated in a 5 point likert scale. An average score will be calculated for each question.

Secondary

MeasureTime frameDescription
change in body weight6 monthsPatients will be asked to remove shoes, socks, heavy clothing and jewelry for measurement of body weight to the nearest 100 g using a digital scale.
Measures of adherence after 6 months6 monthsNumber of patients returning to the outpatient clinic after the intervention.
Calcium Blood Value6 monthsChange in Calcium levels (mg/dL) after 6 months
Iron Blood Value6 monthsChange in Ferritin levels (ng/mL) after 6 months
change in fat free mass6 monthsA Bioelectric impedance analysis will be used to calculate change in fat free mass. Measurements will be conducted by a device sending weak electric signals through the patients body. The method is non-invasive.
Vitamin D Blood Value6 monthsChange in Vitamin D, 25-Hydroxy levels (nmol/L) after 6 months
Folic Acid Blood Value6 monthsChange in Folic Acid levels (nmol/L) after 6 months
HbA1c Blood Value6 monthsChange in Hemoglobin A1c (%) after 6 months
Vitamin B12 Blood Value6 monthsChange in B12 levels (pmol/L) after 6 months

Countries

Austria

Contacts

Primary ContactTamara Ranzenberger-Haider, MSc
tamara.ranzenberger-haider@muv.ac.at00436765202648
Backup ContactMichael Krebs, Prof.Dr.
michael.krebs@muv.ac.at+43 (0)1 40400-72570

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026