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Intervention Study to Prevent Obesity in Sedentary 8 Year Old Swedish Children (STOPP-8)

Primary Purpose

Cardiovascular Risk Factors, Metabolic Risk Factors, Sedentary Lifestyle

Status
Withdrawn
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Motivational Interviewing
Physical activity
Supplementation with fish liver oli capsules
Placebo oil capsules
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Risk Factors focused on measuring accelerometry, physical activity, obesity, children, cardiovascular risk markers, metabolic risk markers, DXA, obesity prevention, omega 3, fish liver oil, motivational interviewing

Eligibility Criteria

7 Years - 9 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Level of physical activity below the 30ieth percentile cut off point derived from a large reference population.

Exclusion Criteria:

  • Family not being able to participate in the program or take part in at least the physical activity assessment.
  • Morbidities that affects the outcome parameters.

Sites / Locations

  • Karolinska Institutet, Dept. of Clinical Science, Intervention and Technology (CLINTEC), Division of Pediatrics.

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Motivational Interviewing and omega 3

Motivational interviewing and placebo

Control and omega 3

Control and placebo

Arm Description

This arm is the group that receives the intervention program and eats fish liver oil capsules. Represents 25 % of all participants.

This arm is the group that receives the intervention program and eats placebo oil capsules. Represents 25 % of all participants.

This arm is the group that does not receives the intervention program and eats fish liver oil capsules. Represents 25 % of all participants.

This arm is the group that does not receives the intervention program and eats placebo oil capsules. Represents 25 % of all participants.

Outcomes

Primary Outcome Measures

Change in level of physical activity
Physical activity, is measured with tri-axis accelerometers of the brand Actigraph model GT3X. Data is collected every 10 seconds during 7 consecutive whole days. It is the most feasible and precise method for the purpose.

Secondary Outcome Measures

Body composition
Dual Energy X-ray Absorbtiometry (body composition and Bone mass density). Brand: General Electronics Health Care; Model: iDXA. It is a non-invasive method using x-ray and computer technology to assess the proportions of fat mass, lean mass and bone mass and to measure the bone mass density. The method is widely used and does not mean any direct increased risk. The amount of x-ray is equivalent to the amount individuals get exposed from their natural environment during an average day in free living conditions.
Cardiovascular risk markers
Blood sample is collected from all participants in the intervention program (all 4 arms). However, this will not be decisive for inclusion in the study. Parents will be thoroughly informed of the procedure of blood sampling (i.e. local anaesthesia) and that they can choose not to participate in this part of the study. Fasting blood samples will be analyzed for LDL-C, HDL-C, tot-C, TG, Lp(a), hsCRP, TNF-α, IL6, IL1, PAI-1, glucose, Apo A-1, Apo B, adiponectin, leptin, insulin, omega-3 and FTO-gene expression.
BMI (Body Mass Index)
The childrens' height and weight is recorded via standardized and calibrated scales and stadiometer.
Quality of life scale
A validated questionnaire including self report for subjective feeling of quality of life are filled out by each child with assistance of an adult (parent or teacher)
Self reported motor skills
A validated questionnaire including self report motor skills e are filled out by each child with assistance of an adult (parent or teacher)
Self reported physical activity
A validated questionnaire including self report for physical activity are filled out by each child with assistance of an adult (parent or teacher)
Physical fitness
An ergometer bicycle test is performed by each child at baseline to assess the level of physical fitness. It is a sub-maximal test performed at a moderate intensity work load during 5 - 8 minutes. This test is performed to characterize the participants and the result (an indirect measure for oxygen uptake capacity and aerobic work capacity) is used to control and adjust the results by.

Full Information

First Posted
March 15, 2010
Last Updated
February 22, 2021
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT01087411
Brief Title
Intervention Study to Prevent Obesity in Sedentary 8 Year Old Swedish Children
Acronym
STOPP-8
Official Title
A Controlled Study Aiming to Increase Physical Activity and Decrease Risk Bio-markers in Sedentary 8 Year Old Swedish Children Via Physical Activity and Fish Liver Oil Supplementation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Withdrawn
Why Stopped
2010 represented complications recruiting. The team suffered from sick-leave.
Study Start Date
October 2008 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to study whether a targeted intervention can increase physical activity in inactive 8-yr old children and how it affects secondary measures such as metabolic- and cardiovascular risk factors and markers, self-reported quality of life, BMI, body composition and aerobic work-capacity.
Detailed Description
Background Between 3 to 5 % of Swedish 10 yr olds are obese and an additional 20 % are over-weight. Being physically inactive in childhood increases the risk for becoming obese both in child- and adulthood and a correlation between BMI and arterial-sclerotic markers can be seen already in childhood. Physical activity (PA) in children improve their insulin sensitivity and reduce metabolic risk regardless of the proportion of fat mass. Published questionnaire data suggests that the level of PA has decreased in children between the years 1968 to 2001. Study aims To study whether a targeted intervention can increase PA in sedentary 8-yr old children (2nd grade Swedish elementary school) and how it affects secondary measures such as; metabolic- and cardiovascular risk markers; self-reported quality of life, PA and motor skills; BMI; body composition; bone mineral density (BMD); PF. To identify factors of success that could be implemented in schools and pre-schools and in the commune and health-care parent support. Subjects and methods With informed written consent of parents/caretakers we will screen at selected schools with questionnaires and accelerometers to identify sedentary children. The 30% most inactive children will be offered participation in the study. Cut off values for inactivity is obtained from a large reference-material based on 1800 measurements on 6 - 10 yr old children from the STOPP study. The intervention will be delivered through sessions aiming at developing healthy habits regarding PA and via supplementation with fish liver oil. The sessions will be performed by trained health workers (coaches) and carried out in the families' homes and later on via telephone. All families will meet with their coach during at least 6 times. The coaches will use the technique of Motivational Interviewing (MI). However, extra efforts, such as group work-out sessions and out-door activities, will be made. The individual work with these families is delicate and the intervention staff group will therefore have continuous education and guidance from a qualified MI tutor. All included children will be randomized to equally sized intervention or control group. All outcome measures will be assessed at 0 and 15 weeks (completion) of the intervention. The study is limited by the school semesters. Screening is therefore scheduled to the fall- and intervention program to spring semester.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Risk Factors, Metabolic Risk Factors, Sedentary Lifestyle, Overweight
Keywords
accelerometry, physical activity, obesity, children, cardiovascular risk markers, metabolic risk markers, DXA, obesity prevention, omega 3, fish liver oil, motivational interviewing

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Motivational Interviewing and omega 3
Arm Type
Experimental
Arm Description
This arm is the group that receives the intervention program and eats fish liver oil capsules. Represents 25 % of all participants.
Arm Title
Motivational interviewing and placebo
Arm Type
Experimental
Arm Description
This arm is the group that receives the intervention program and eats placebo oil capsules. Represents 25 % of all participants.
Arm Title
Control and omega 3
Arm Type
Experimental
Arm Description
This arm is the group that does not receives the intervention program and eats fish liver oil capsules. Represents 25 % of all participants.
Arm Title
Control and placebo
Arm Type
Placebo Comparator
Arm Description
This arm is the group that does not receives the intervention program and eats placebo oil capsules. Represents 25 % of all participants.
Intervention Type
Behavioral
Intervention Name(s)
Motivational Interviewing
Intervention Description
The method motivational interviewing according to Miller and Rollnik is used as an behavioral intervention to support the child and family in their own behavioral change towards a more physically active life style.
Intervention Type
Behavioral
Intervention Name(s)
Physical activity
Intervention Description
Group sessions with different kinds of physical activity is arranged for the participants in the intervention program.
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplementation with fish liver oli capsules
Intervention Description
This group will receive capsules containing omega-3 and omega-6 fatty acids and vitamine E. The dosage is six capsules daily containing omega-3 (558 mg of eico-pentaenoic-acid, EPA, and 174 mg of docosahexaenoic acid, DHA), omega-6 (60 mg of γ-linolenic acid, GLA) plus 9.6 mg vitamin E (in natural form, d-α-tocopherol), gelatin and glycerol. Participants will be instructed to eat three capsules each morning and evening.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo oil capsules
Intervention Description
This group will receive capsules containing rape seed oil. Participants will be instructed to lead their life in the same manner as before the intervention but eat three capsules each morning and evening.
Primary Outcome Measure Information:
Title
Change in level of physical activity
Description
Physical activity, is measured with tri-axis accelerometers of the brand Actigraph model GT3X. Data is collected every 10 seconds during 7 consecutive whole days. It is the most feasible and precise method for the purpose.
Time Frame
screening, 0 and 15 weeks and 12 months
Secondary Outcome Measure Information:
Title
Body composition
Description
Dual Energy X-ray Absorbtiometry (body composition and Bone mass density). Brand: General Electronics Health Care; Model: iDXA. It is a non-invasive method using x-ray and computer technology to assess the proportions of fat mass, lean mass and bone mass and to measure the bone mass density. The method is widely used and does not mean any direct increased risk. The amount of x-ray is equivalent to the amount individuals get exposed from their natural environment during an average day in free living conditions.
Time Frame
0 and 15 weeks
Title
Cardiovascular risk markers
Description
Blood sample is collected from all participants in the intervention program (all 4 arms). However, this will not be decisive for inclusion in the study. Parents will be thoroughly informed of the procedure of blood sampling (i.e. local anaesthesia) and that they can choose not to participate in this part of the study. Fasting blood samples will be analyzed for LDL-C, HDL-C, tot-C, TG, Lp(a), hsCRP, TNF-α, IL6, IL1, PAI-1, glucose, Apo A-1, Apo B, adiponectin, leptin, insulin, omega-3 and FTO-gene expression.
Time Frame
0 and 15 seeks
Title
BMI (Body Mass Index)
Description
The childrens' height and weight is recorded via standardized and calibrated scales and stadiometer.
Time Frame
0 and 15 weeks
Title
Quality of life scale
Description
A validated questionnaire including self report for subjective feeling of quality of life are filled out by each child with assistance of an adult (parent or teacher)
Time Frame
0 and 15 weeks
Title
Self reported motor skills
Description
A validated questionnaire including self report motor skills e are filled out by each child with assistance of an adult (parent or teacher)
Time Frame
0 and 15 weeks
Title
Self reported physical activity
Description
A validated questionnaire including self report for physical activity are filled out by each child with assistance of an adult (parent or teacher)
Time Frame
0 and 15 weeks
Title
Physical fitness
Description
An ergometer bicycle test is performed by each child at baseline to assess the level of physical fitness. It is a sub-maximal test performed at a moderate intensity work load during 5 - 8 minutes. This test is performed to characterize the participants and the result (an indirect measure for oxygen uptake capacity and aerobic work capacity) is used to control and adjust the results by.
Time Frame
0 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Level of physical activity below the 30ieth percentile cut off point derived from a large reference population. Exclusion Criteria: Family not being able to participate in the program or take part in at least the physical activity assessment. Morbidities that affects the outcome parameters.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pernilla Danielsson Liljeqvist, MD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institutet, Dept. of Clinical Science, Intervention and Technology (CLINTEC), Division of Pediatrics.
City
Huddinge
State/Province
Södermanland
ZIP/Postal Code
14186
Country
Sweden

12. IPD Sharing Statement

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Intervention Study to Prevent Obesity in Sedentary 8 Year Old Swedish Children

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