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The Odense Overweight Intervention Study (OOIS)

Primary Purpose

Children, Overweight, Obesity

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Small intervention
Intervention camp
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Children focused on measuring Children, Overweight, Obesity, BMI, Physical activity, Cognitive function, Intervention study, Randomized controlled trial, Day camp, Risk factors

Eligibility Criteria

10 Years - 13 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children in the municipality of Odense, Denmark
  • Overweight or obese (BMI) according to the International Obesity Task Force

Exclusion Criteria:

  • Children who are participating in other research based intervention programmes related to risk factors of heart diseases.
  • Children who are following a special school programme.
  • Use of weight reducing medicine within 3 months before the baseline measurements
  • Children with a motor skill determined handicap of such complexity that it hinders them from participating in the intervention.

Sites / Locations

  • Odense University Hospital
  • University of Southern Denmark

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Intervention camp

Small intervention

Arm Description

Children's behavior are controlled each week day for six weeks, and children participate in three hours of physical activity every day

Children are only informed of healthy behavior

Outcomes

Primary Outcome Measures

Change in BMI From Baseline to 12 Months Follow up.
Change in Body Mass Index (BMI) for each intervention arm from baseline (4-6 weeks prior to intervention) to 12 months follow up. BMI is defined as kg/m^2. Although three measurements have been conducted, we only report the first and last.

Secondary Outcome Measures

Change in Cognitive Function From Baseline to 12 Months Follow up.
To assess cognitive function the following test are used: The Stroop Color and word test; Trail making test (part A and B); Rey complex figure test and recognition trial; Symbol digit modalities Test; Behavior rating inventory of executive function.
Change in Motor Skills From Baseline to 12 Months Follow up.
To assess motor skills, the Movement Assesment Battery for Children 2 (Movement ABC-2) test for 11-16 year olds was applied. The battery allows for recording a number of different aspects of a child's movement skills in a systematic way. In this study we only used the quantitative part of the test (it also includes a qualitative part). This includes 3 tests for hand skills (fine motor skills), 2 tests for throwing and catching balls, and 3 tests for balance skills. Each subtest returns a score, which is summarized and then equivalent to a percentile score (based on norm data from a standard population in a table from the Movement ABC-2 compendium). The percentile score is reported as the overall motor skills. The scale is from 0.1 to 99.9 (normal distributed with an average of 50) and higher scores mean better motor skills.
Change in Body Composition From Baseline to 12 Months Follow up.
Measurements of fat mass and lean tissue mass using dual-energy X-ray absorptiometry.
Change From Baseline in Brain-derived Neurotrophic Factor (BDNF) at 12 Months.
The chronic level of serum brain-derived neurotrophic factor (BDNF) is assessed in fasting blood samples.
Change From Baseline in Blood Pressure at 12 Months.
Blood pressure will be measured in up-right sitting position after resting supine for ten minutes. A minimum of five measurements will be conducted with one minute intervals.
Change From Baseline in Subclinical Atherosclerosis Using B-mode Ultrasound: Carotid Intima Media Thickness and Carotid Elasticity at 12 Months.
The Carotid Intima Media and Carotid Elasticity are measured on 2 sites (posterior and lateral) of the far wall 1 cm proximal to the bifurcation on both sides of the common carotid artery.
Change From Baseline in Cardio-respiratory Fitness at 12 Months.
Cardio-respiratory fitness will be assessed using a progressive bicycle ergometer protocol after a 5 minutes warm-up by means of indirect calorimetry (Innovision, Odense, Denmark).
Change From Baseline in Insulin Level at 12 Months.
The level of insulin is assessed in fasting blood samples.
Change From Baseline in Glucose Level at 12 Months.
The level of glucose is assessed in fasting blood samples.
Change From Baseline in Blood Lipids at 12 Months.
The levels of lipids are assessed in fasting blood samples.
Change From Baseline in C-Reactive Protein at 12 Months.
The level of c-reactive-protein is assessed in fasting blood samples.
Change From Baseline in Waist/Hip Circumference at 12 Months.
Hip circumference will be measured at the level of the great trochanter. Waist circumference will be measured between the lower costal margin and the iliac crest.
Change in Clustered Cardiovascular Disease (CVD) Risk Factor
The CVD risk factor is the mutual presence of five different health outcomes based on the Metabolic Syndrome. It is calculated by creating a composite risk score (mean of z-scores) of: 1) Insulin resistance (Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)), 2) Systolic blood pressure, 3) triglyceride, 4) total cholesterol/HDL ratio, 5) Abdominal fatness (by Dual-energy X-ray absorptiometry (DXA)), and 6) aerobic fitness.
Change From Baseline in Physical Strength at 12 Months.
Will be measured by hand grip and Sargent vertical jump.

Full Information

First Posted
March 26, 2012
Last Updated
November 14, 2020
Sponsor
University of Southern Denmark
Collaborators
TrygFonden, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT01574352
Brief Title
The Odense Overweight Intervention Study
Acronym
OOIS
Official Title
The Odense Overweight Intervention Study (OOIS): A Randomized Controlled Trial on Overweight Prevention in Children.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 2012 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
TrygFonden, Denmark

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Strong and consistent evidence have shown that overweight, including obesity, is an important risk factor for the development of cardiovascular disease (CVD) in adults. Several studies have found an association between overweight in childhood and increased risk of morbidity and mortality later in life. The prevalence of overweight in children and adolescents has increased in recent years, and consequently it is important to identify effective approaches in the prevention and treatment of overweight in young individuals. Approaches such as resident weight loss camps have shown promising results. A residential camp setting provides an opportunity to increase and control exposure to, for instance, particular foodstuffs, beverages and physical activity opportunities. However, well-designed studies with sufficient participants are still needed on the reversal of overweight in childhood with increased focus on documenting predictors of behavior changes associated with decreases in overweight. This study is carried through as a randomized controlled trial which investigates the effect of participating in a 6 week health promoting resident for overweight fifth grade children camp followed by 46 weeks of family support. The study hypothesis is that participating in a 6 week resident camp and a following period of 46 weeks of child and family support will induce a reduction in body mass index (BMI). In addition it is expected that the intensity and duration intervention program is sufficient to cause changes in physiological parameters related to a reduced risk of lifestyle diseases.
Detailed Description
Intervention type 1: Day camp and resident camp: The intervention is divided into two parts - an intensive six week day or resident camp with a subsequent ten month follow-up intervention program. The children participate in a six week day camp where they are engaged in fun-based physical activity and sports, health classes as well as math lessons, Danish language and science classes. All classes are planned and conducted by health professionals and specialist instructors. All physical activity classes are primarily held using outdoor recreational facilities such as soccer fields, basketball courts, and forest areas within bicycling distance to the camp. Three hours of physical activity and sports are scheduled every day, and the classes are designed to reinforce motor skills, fitness, muscle strength, and confidence within the sporting environment. The planned sports activities are both competitive and non-competitive providing the children with both positive experiences in relation to physical activity and tools to cope with competitive situations in their normal environment including commuter bicycling. Bicycles are available for all children. Beside scheduled physical activity the children are encouraged to stay physically active during breaks and leisure time. Six hours a week health classes with the purpose of increasing their knowledge on health issues such as the benefits of a healthy diet and sports participation and increasing body awareness are scheduled. The classes consist of nutritional training, physiology, exercise and goal setting. For this purpose "Appreciative Inquiry" (AI) is used. Briefly, this deals with inquiry into and dialogue about strengths, successes, values, hopes and dreams related to lifestyle behaviors. The nutritional education consists of theoretical education in the national Danish dietary recommendations in combination with personal guidance at every meal. At the camp food intake is prepared and served according to the national Danish dietary recommendations.(15) The actual eating situation is supervised and guided by specialist instructors, but no calorie restriction is enforced. All camp staff will receive extensive training by specialist instructors with in the field of pedagogic and psychology. Intervention arm specifications: Children allocated to this intervention arm will stay at a day camp from 7 a.m. to 8.30 p.m. seven days a week during six weeks including transportation to the day camp. The children will stay at home with their parents outside this time period. The camp is located in the city of Odense, Denmark. The children, together with their family, participate in an initial counseling session. The aim is to support the participants in their efforts to uphold the designed program on diet and food intake. Following this session, the families sign a so-called commitment contract confirming their continuing involvement. During the intervention, text messages will be sent to the children in order to help them comply with the program, and the parents will receive a handbook on dietary recommendations. The children will commute using bicycles to and from the school camp in combination with parent transportation. The children will commute in smaller groups arranged according to the residential area. Active commuting will be supervised and arranged by the camp instructors. Parent transportation will be coordinated by the camp staff. Early parent involvement - Intervention and Satellite arm: In the beginning of the intervention a parent council is founded. Experiences from the resident camp project have revealed a positive influence regarding networking and general parent involvement and support due to the foundation of an active parent council (personal communication). During the day camp the families are offered a dietary course, led by a dietician, consisting of 3x2 hour meetings. Themes at the course are; Healthy cooking, Grocery Shopping, Healthy Eating Patterns in their every day context and parental influence on physical activity behavior. The subsequent family-based intervention- Intervention and Satellite arm: After the six week intervention, a family based intervention consisting of four meetings will be planned with the family (the participant and their parents/legal guardian) targeting physical activity and dietary behavior delivered by school health nurses and teachers from the day camp intervention. The following four themes will be attended during the four meetings: "Everyday diet for the family", "Active transport and sports participation", "Weight management in the family" and "Networking and support". Appreciative Inquiry (AI) will be used as a method to equip families with a method to handle challenges related to the targeted behaviors. At all meetings the families will discuss and share experiences related to the central topic of the meeting. The children must be accompanied by at least one parent or legal guardian during the meetings. The investigators have had promising results and feedback from children and families as regards using AI during the family based intervention in the pilot study. Intervention type 2- control group: Standard intervention: Children allocated to this intervention will receive a standard intervention, which consist of: 1) one weekly physical activity session (one hour duration) for six weeks arranged by the municipality; 2) two educational sessions, delivered by a dietician and physical activity specialist, for the parents concerning diet and physical activity behavior.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Children, Overweight, Obesity, Metabolic Syndrome
Keywords
Children, Overweight, Obesity, BMI, Physical activity, Cognitive function, Intervention study, Randomized controlled trial, Day camp, Risk factors

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
115 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention camp
Arm Type
Experimental
Arm Description
Children's behavior are controlled each week day for six weeks, and children participate in three hours of physical activity every day
Arm Title
Small intervention
Arm Type
Experimental
Arm Description
Children are only informed of healthy behavior
Intervention Type
Behavioral
Intervention Name(s)
Small intervention
Other Intervention Name(s)
control group
Intervention Description
The control group are offered a weekly 1 hour training or activity session during six weeks. Furthermore two sessions where the parents are invited to participate in information about diet and exercise.
Intervention Type
Behavioral
Intervention Name(s)
Intervention camp
Other Intervention Name(s)
Behavioral intervention, Camp intervention, Physical activity intervention
Intervention Description
The children are participating in a 6 week day camp. The camp contains social activities, physical activity training, usual school classes and health education. All meals (healthy food) are consumed during the camp day.
Primary Outcome Measure Information:
Title
Change in BMI From Baseline to 12 Months Follow up.
Description
Change in Body Mass Index (BMI) for each intervention arm from baseline (4-6 weeks prior to intervention) to 12 months follow up. BMI is defined as kg/m^2. Although three measurements have been conducted, we only report the first and last.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Secondary Outcome Measure Information:
Title
Change in Cognitive Function From Baseline to 12 Months Follow up.
Description
To assess cognitive function the following test are used: The Stroop Color and word test; Trail making test (part A and B); Rey complex figure test and recognition trial; Symbol digit modalities Test; Behavior rating inventory of executive function.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change in Motor Skills From Baseline to 12 Months Follow up.
Description
To assess motor skills, the Movement Assesment Battery for Children 2 (Movement ABC-2) test for 11-16 year olds was applied. The battery allows for recording a number of different aspects of a child's movement skills in a systematic way. In this study we only used the quantitative part of the test (it also includes a qualitative part). This includes 3 tests for hand skills (fine motor skills), 2 tests for throwing and catching balls, and 3 tests for balance skills. Each subtest returns a score, which is summarized and then equivalent to a percentile score (based on norm data from a standard population in a table from the Movement ABC-2 compendium). The percentile score is reported as the overall motor skills. The scale is from 0.1 to 99.9 (normal distributed with an average of 50) and higher scores mean better motor skills.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change in Body Composition From Baseline to 12 Months Follow up.
Description
Measurements of fat mass and lean tissue mass using dual-energy X-ray absorptiometry.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Brain-derived Neurotrophic Factor (BDNF) at 12 Months.
Description
The chronic level of serum brain-derived neurotrophic factor (BDNF) is assessed in fasting blood samples.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Blood Pressure at 12 Months.
Description
Blood pressure will be measured in up-right sitting position after resting supine for ten minutes. A minimum of five measurements will be conducted with one minute intervals.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Subclinical Atherosclerosis Using B-mode Ultrasound: Carotid Intima Media Thickness and Carotid Elasticity at 12 Months.
Description
The Carotid Intima Media and Carotid Elasticity are measured on 2 sites (posterior and lateral) of the far wall 1 cm proximal to the bifurcation on both sides of the common carotid artery.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Cardio-respiratory Fitness at 12 Months.
Description
Cardio-respiratory fitness will be assessed using a progressive bicycle ergometer protocol after a 5 minutes warm-up by means of indirect calorimetry (Innovision, Odense, Denmark).
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Insulin Level at 12 Months.
Description
The level of insulin is assessed in fasting blood samples.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Glucose Level at 12 Months.
Description
The level of glucose is assessed in fasting blood samples.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Blood Lipids at 12 Months.
Description
The levels of lipids are assessed in fasting blood samples.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in C-Reactive Protein at 12 Months.
Description
The level of c-reactive-protein is assessed in fasting blood samples.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Waist/Hip Circumference at 12 Months.
Description
Hip circumference will be measured at the level of the great trochanter. Waist circumference will be measured between the lower costal margin and the iliac crest.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change in Clustered Cardiovascular Disease (CVD) Risk Factor
Description
The CVD risk factor is the mutual presence of five different health outcomes based on the Metabolic Syndrome. It is calculated by creating a composite risk score (mean of z-scores) of: 1) Insulin resistance (Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)), 2) Systolic blood pressure, 3) triglyceride, 4) total cholesterol/HDL ratio, 5) Abdominal fatness (by Dual-energy X-ray absorptiometry (DXA)), and 6) aerobic fitness.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.
Title
Change From Baseline in Physical Strength at 12 Months.
Description
Will be measured by hand grip and Sargent vertical jump.
Time Frame
Assessed on 2 occasions: 1) Baseline measurements: 4 - 6 weeks before initiation of interventions. 2) 2nd follow up: 52-53 weeks (12 months) after initiation of interventions.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children in the municipality of Odense, Denmark Overweight or obese (BMI) according to the International Obesity Task Force Exclusion Criteria: Children who are participating in other research based intervention programmes related to risk factors of heart diseases. Children who are following a special school programme. Use of weight reducing medicine within 3 months before the baseline measurements Children with a motor skill determined handicap of such complexity that it hinders them from participating in the intervention.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Bo Andersen, Professor
Organizational Affiliation
Center of Research in Childhood Health (RICH), University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Odense University Hospital
City
Odense
State/Province
Funen
ZIP/Postal Code
5000
Country
Denmark
Facility Name
University of Southern Denmark
City
Odense
State/Province
Funen
ZIP/Postal Code
5230
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data is available on request from The Danish National Archives (http://dda.dk/catalogue/30519) after August 2016.
IPD Sharing Time Frame
After August 2016
IPD Sharing Access Criteria
Data can only be used for scientific and statistical aims and reporting of aggregated information. Not for investigating affairs of private individuals or organisations. Data can under any circumstances be passed on to a third party, but only be utilized by the user(s) from the project application. Data can only be used for the purposes stated in the project application for the Danish National Archives. Considerable changes of the aim will require a new application. Any publication using the data from the project must bibliographically correct credit the Danish National Archives as well as the principal investigator. Publications must be send to the mailbox og the Danish National Archives attached as a file. The Danish National Archives will forward a copy to the principal investigator. After utilization of the data it must be deleted or returned to the Danish National Archives.
IPD Sharing URL
http://dda.dk/catalogue/30519
Citations:
PubMed Identifier
34180245
Citation
Thomsen CF, Goharian TS, Larsen KT, Goetze JP, Andersen LB, Jeppesen JL. Intensive Lifestyle Intervention Increases Plasma Midregional Proatrial Natriuretic Peptide Concentrations in Overweight Children. J Am Heart Assoc. 2021 Jul 6;10(13):e020676. doi: 10.1161/JAHA.121.020676. Epub 2021 Jun 28.
Results Reference
derived
PubMed Identifier
27416906
Citation
Larsen KT, Huang T, Larsen LR, Olesen LG, Andersen LB, Moller NC. The effect of a multi-component camp-based weight-loss program on children's motor skills and physical fitness: a randomized controlled trial. BMC Pediatr. 2016 Jul 15;16:91. doi: 10.1186/s12887-016-0627-5.
Results Reference
derived
PubMed Identifier
24708676
Citation
Larsen KT, Huang T, Moller NC, Andersen LB, Ried-Larsen M. Effectiveness of a one-year multi-component day-camp intervention for overweight children: study protocol of the Odense overweight intervention study (OOIS). BMC Public Health. 2014 Apr 5;14:313. doi: 10.1186/1471-2458-14-313.
Results Reference
derived
Links:
URL
http://www.sdu.dk/om_sdu/institutter_centre/iob_idraet_og_biomekanik
Description
Institute of Sports Science and Clinical Biomechanics, University of Southern Denmark

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The Odense Overweight Intervention Study

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