Low-level Intervention for Adolescents With Extreme Obesity (STEREO)
Primary Purpose
Obesity, Extreme Obesity
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
manual based low key group intervention (innovation)
standardized, manual based routine care
Sponsored by

About this trial
This is an interventional treatment trial for Obesity focused on measuring Extreme Obesity Keywords: obesity, adiposity, psychosocial, healthcare, co-morbidities, low key intervention, quality of life
Eligibility Criteria
Inclusion Criteria:
- BMI ≥30kg/m2
- sufficient German language skills
Exclusion Criteria:
- Circumstances that require immediate inpatient care (e.g. severe somatic or psychiatric illness)
- obvious cognitive disability
Sites / Locations
- Ambulatory Obesity Program, Charité University, Berlin
- Vestische Kinderklinik, University of Witten/Herdecke
- Center for Clinical Trials Essen
- University Duisburg-Essen
- University Hospital Leipzig
- Dept for Pediatrics and Adolescent Medicine, University of Ulm: Interdisciplinary obesity clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
low key intervention
routine care
Arm Description
Outcomes
Primary Outcome Measures
Composite primary endpoint (tested hierarchically) of a) compliance rate and b) changes in health related quality of life.
a) Number of regular participants at 6 months follow up will be divided by number of participants at baseline. b) Changes (randomization - 6 months follow up) in the 37 item DISABKIDS questionnaire will be assessed.
Secondary Outcome Measures
Changes in the 6 subscales of DISABKIDS
The 37 item DISABKIDS questionnaire will be applied twice, and the score difference in each of the 6 subscales will be calculated for each subject.
Changes in quality of life
The 52 item KIDSCREEN-52 questionnaire will be applied twice, and the score difference will be calculated for each subject.
Changes in self-esteem
The Rosenberg's scale patient questionnaire will be applied twice, and the score difference will be calculated for each subject.
Changes in self reported time spent outside the home
The time spent outside the home will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the time difference will be calculated for each subject.
Changes in depression symptoms
The Becks Depression Inventory 2 questionnaire will be applied twice, and the score difference will be calculated for each subject. Answers will be reviewed immediately to identify and treat subjects at risk for self harm.
Changes in perceived stress
The Fliege scale questionnaire will be applied twice, and the score difference will be calculated for each subject.
Changes in the self reported attendance of school, apprenticeship, or work
The attendance of school, apprenticeship, or work will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the time difference will be calculated for each subject.
Changes in self reported physician- / and therapist contacts
Physician- / and therapist contacts will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the difference will be calculated for each subject.
Full Information
NCT ID
NCT01703273
First Posted
August 7, 2012
Last Updated
June 12, 2018
Sponsor
Prof. Dr. Martin Wabitsch
Collaborators
University of Witten/Herdecke, Charite University, Berlin, Germany, University of Leipzig, Universität Duisburg-Essen, University of Ulm, Zentrum für klinische Studien Essen
1. Study Identification
Unique Protocol Identification Number
NCT01703273
Brief Title
Low-level Intervention for Adolescents With Extreme Obesity
Acronym
STEREO
Official Title
Structured Low-level Intervention vs. Treatment as Usual Evaluated in a Randomized Controlled Trial for Adolescents With Extreme Obesity, Subproject 2
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
July 2012 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Dr. Martin Wabitsch
Collaborators
University of Witten/Herdecke, Charite University, Berlin, Germany, University of Leipzig, Universität Duisburg-Essen, University of Ulm, Zentrum für klinische Studien Essen
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
While adolescents with obesity and extreme obesity are at increased risk for health complications, especially adolescents with extreme obesity rarely seek medical care, and sustained weigh loss is hardly ever achieved. One of the underlying reasons might be the lack of adequate treatment options.
In this multicenter study, we aim to test a new, low key group intervention focusing on improving compliance and psychosocial functioning. The study is a subproject of the Medical and psychosocial implications of adolescent extreme obesity - acceptance and effects of structured care, short: "Youth with Extreme obesity Study (YES)", which aims at improving the medical care and social support structures for youth with obesity and extreme obesity in Germany.
Obese youth and young adults (BMI ≥ 30kg/m2) between the ages of 14 and 24.9 years (initially up to 21 years) are eligible to participate. Participants will be asked to complete a series of questionnaires on their general health, psychosocial situation and wellbeing, and will be offered a thorough medical evaluation. Individuals who complete the baseline evaluations will be invited to participate in 6 group sessions over a 3 months period. Group assignment to the psycho-social intervention vs. routine care group will be at random, like throwing a dice. After 6 months, participants will complete further questionnaires to evaluate the effects of the interventions on quality of life and psycho-social functionning.
The study will show the acceptance and effectiveness of a new intervention focusing on improving compliance and psychosocial functioning in adolescents with extreme obesity, and thereby inform the development of new treatment and support options for these adolescents. If interested, participants are invited to participate in additional components of YES, and to receive medical care and psycho-social support.
Detailed Description
While obese youth are at high risk for co-morbidities, especially the extremely obese individuals rarely seek medical care. The underlying reasons are poorly understood, but patient inherent factors and the lack of adequate treatment options may play a role.
In this multicenter study, we aim to assess the acceptance and effectiveness of a manual based low key group intervention focusing on improving compliance and psychosocial functioning in adolescents with morbid obesity (BMI≥35kg/m2), in comparison to routine care. Youth with more moderate degrees of obesity (BMI 30-34.9kg/m2) will serve as an additional control group. The study is part of the Medical and psychosocial implications of adolescent extreme obesity - acceptance and effects of structured care", short: "Youth with extreme obesity Study (YES), which also comprises the recruitment and characterization of obese (BMI 30-34.9kg/m2) and extremely obese (BMI ≥ 35kg/m2) youth from different healthcare- and non healthcare settings, a structured prospective evaluation of adolescent bariatric surgery, economic assessments of the financial burden of extreme adolescent obesity on the healthcare system, and a long-term prospective observation study.
Based on the current state of knowledge, we will test the a priori ordered hirarchy of hypotheses:
The compliance rate 6 months after randomization is higher in subjects in the low key intervention group compared to the standard care group.
Covariant-adjusted changes in quality of life (assessed by DISABKIDS scale) between baseline and the 6 months follow up will be more pronounced in the low key intervention group compared to the standard care group.
The five participating university centers are distributed across 4 geographic regions in the North (Berlin), in the West (Essen/Datteln), in the East (Leipzig) and in the South (Ulm) of Germany, and will therefore render data that are representative of Germany as a whole. We will screen a 600 adolescents age 14 to 24.9 years (initially up to 21 years; this was changed in an amendment in February 2013) with extreme obesity (BMI ≥ 35 kg/m2) and 600 adolescents with obesity (BMI 30-34.9 kg/m2) over a 24 months period. A total of 350 subjects will be enrolled. Baseline assessments include an array of standardized questionnaires and validated instruments to assess health, psycho-social situation, psychiatric co-morbidities and health related quality of life, as well as an in-depth medical evaluation. Individuals who complete the baseline evaluations will be invited to participate in 6 group sessions over a 3 months period. Group assignment to the low key intervention vs. standard care group will be at random. The effects of the interventions on health related quality of life and psycho-social functioning will be assessed via questionnaires after 6 months. Subsequently, subjects will be invited to participate in additional components of YES.
The project will reveal the effectiveness and safety of a manual based low key group intervention focusing on improving compliance and psychosocial functioning in adolescents with morbid obesity, and thereby inform the development of new treatment and support options for these adolescents in Germany.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Extreme Obesity
Keywords
Extreme Obesity Keywords: obesity, adiposity, psychosocial, healthcare, co-morbidities, low key intervention, quality of life
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
119 (Actual)
8. Arms, Groups, and Interventions
Arm Title
low key intervention
Arm Type
Experimental
Arm Title
routine care
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
manual based low key group intervention (innovation)
Intervention Description
6 sessions offered over the course of 3-6 months focus on improvement of quality of life and psychosocial functioning . Topics covered are: 1) social competencies, 2) body image, 3) coping with mobbing and anger, 4) coping with stress, 5) life satisfaction, and 6) psychological well being. The planned intervention does not primarily focus on weight loss.
Intervention Type
Behavioral
Intervention Name(s)
standardized, manual based routine care
Intervention Description
6 sessions offered over the course of 3-6 months with a focus on weight loss. The topics 1) causes, consequences and treatment options of obesity, 2) nutrition, 3) eating behaviors and problem solving strategies, 4) self esteem and emotional eating, 5) exercise, and 6) use of media, will be covered.
Primary Outcome Measure Information:
Title
Composite primary endpoint (tested hierarchically) of a) compliance rate and b) changes in health related quality of life.
Description
a) Number of regular participants at 6 months follow up will be divided by number of participants at baseline. b) Changes (randomization - 6 months follow up) in the 37 item DISABKIDS questionnaire will be assessed.
Time Frame
baseline and 6 months
Secondary Outcome Measure Information:
Title
Changes in the 6 subscales of DISABKIDS
Description
The 37 item DISABKIDS questionnaire will be applied twice, and the score difference in each of the 6 subscales will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in quality of life
Description
The 52 item KIDSCREEN-52 questionnaire will be applied twice, and the score difference will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in self-esteem
Description
The Rosenberg's scale patient questionnaire will be applied twice, and the score difference will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in self reported time spent outside the home
Description
The time spent outside the home will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the time difference will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in depression symptoms
Description
The Becks Depression Inventory 2 questionnaire will be applied twice, and the score difference will be calculated for each subject. Answers will be reviewed immediately to identify and treat subjects at risk for self harm.
Time Frame
baseline and 6 months
Title
Changes in perceived stress
Description
The Fliege scale questionnaire will be applied twice, and the score difference will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in the self reported attendance of school, apprenticeship, or work
Description
The attendance of school, apprenticeship, or work will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the time difference will be calculated for each subject.
Time Frame
baseline and 6 months
Title
Changes in self reported physician- / and therapist contacts
Description
Physician- / and therapist contacts will be elicited twice via standardized patient questionnaire (modified after KIGGS and TeenLABS), and the difference will be calculated for each subject.
Time Frame
baseline and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
BMI ≥30kg/m2
sufficient German language skills
Exclusion Criteria:
Circumstances that require immediate inpatient care (e.g. severe somatic or psychiatric illness)
obvious cognitive disability
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin Wabitsch, Prof. Dr. med.
Organizational Affiliation
University of Ulm
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Susanna Wiegand, Dr. med.
Organizational Affiliation
Charite University, Berlin, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Reinehr, Prof. Dr. med.
Organizational Affiliation
University of Witten/Herdecke
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Johannes Hebebrand, Prof. Dr. med.
Organizational Affiliation
Universität Duisburg-Essen
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Wieland Kiess, Prof. Dr. med.
Organizational Affiliation
University of Leipzig
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ambulatory Obesity Program, Charité University, Berlin
City
Berlin
ZIP/Postal Code
13353
Country
Germany
Facility Name
Vestische Kinderklinik, University of Witten/Herdecke
City
Datteln
Country
Germany
Facility Name
Center for Clinical Trials Essen
City
Essen
ZIP/Postal Code
45122
Country
Germany
Facility Name
University Duisburg-Essen
City
Essen
ZIP/Postal Code
45147
Country
Germany
Facility Name
University Hospital Leipzig
City
Leipzig
ZIP/Postal Code
04103
Country
Germany
Facility Name
Dept for Pediatrics and Adolescent Medicine, University of Ulm: Interdisciplinary obesity clinic
City
Ulm
ZIP/Postal Code
89075
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
28787738
Citation
Muhlig Y, Scherag A, Bickenbach A, Giesen U, Holl R, Holle R, Kiess W, Lennerz B, Lutke Brintrup D, Moss A, Neef M, Ose C, Reinehr T, Teuner CM, Wiegand S, Wolters B, Wabitsch M, Hebebrand J. A Structured, Manual-Based Low-Level Intervention vs. Treatment as Usual Evaluated in a Randomized Controlled Trial for Adolescents with Extreme Obesity - the STEREO Trial. Obes Facts. 2017;10(4):341-352. doi: 10.1159/000475717. Epub 2017 Aug 9.
Results Reference
derived
PubMed Identifier
23987123
Citation
Wabitsch M, Moss A, Reinehr T, Wiegand S, Kiess W, Scherag A, Holl R, Holle R, Hebebrand J. Medical and psychosocial implications of adolescent extreme obesity - acceptance and effects of structured care, short: Youth with Extreme Obesity Study (YES). BMC Public Health. 2013 Aug 29;13:789. doi: 10.1186/1471-2458-13-789.
Results Reference
derived
Links:
URL
http://www.adipositasforschung-ulm.de/index.php?id=69
Description
study homepage
Learn more about this trial
Low-level Intervention for Adolescents With Extreme Obesity
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