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PreDictor Research in Obesity during Medical care - weight Loss in children and adolescents during an INpatient rehabilitation- the DROMLIN study

PreDictor Research in Obesity during Medical care - weight Loss in children and adolescents during an INpatient rehabilitation- the DROMLIN study - DROMLIN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00005122
Enrollment
87
Registered
2013-07-03
Start date
2012-02-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Obesity in childhood and adolescence E65-E68

Interventions

Group 1: Children and adolescents (8 to 17 years old) with an indication for hospitalization with the purpose of weight loss will be recruited for a series of investigations. The examinations are perf

Sponsors

Universitäsklinikum Tübingen, Innere Medizin VI, Psychosomatische Medizin und Psychotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 17 Years

Inclusion criteria

Inclusion criteria: Children and adolescents with an indication for hospitalization with the purpose of weight loss - as set by their responsible primary or secondary care physicians - and with a BMI scoring higher than the 97th, resp. of the age and sex specific percentile were included. The reference group has normal weight and is matched for sex and age

Exclusion criteria

Exclusion criteria: Children with severe psychiatric comorbidities, with linguistic or intellectual limitations, type-1 diabetes, tumors, systemic disorders, or severe cardiovascular diseases are excluded from participation. If written informed consent is not provided bei either the child and/or the legal quardian, this is also an exclusion criterion. For the reference group, overweight is also an exclusion criterion.

Design outcomes

Primary

MeasureTime frame
Primary outcome is the change of the body mass index standard deviation score (BMI-SDS). Body weight and body height are assessed upon admission, and prior to discharge using calibrated instruments.

Secondary

MeasureTime frame
Secondary Outcomes are 1) the change of body composition, assessed upon admission and prior to discharge using a lipometer and 2) the change of motor performance assessed upon admission and prior to discharge using the Dordel-Koch-Test

Countries

Germany

Contacts

Public ContactIsabelle Mack

Universitätsklinikum Tübingen, Innere Medizin VI, Psychosomatische Medizin und Psychotherapie

isabelle.mack@medizin.uni-tuebingen.de+49 70712985614

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 19, 2026