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Treatment of Severely Obese Children and Adolescents Employing "Family-based Behavioral Social Facilitation Treatment"

Primary Purpose

Childhood Obesity

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Family-based behavioral social facilitation therapy
TAU - Treatment as usual
Sponsored by
University of Bergen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Childhood Obesity focused on measuring Treatment, Child, Obesity, Behavioral treatment

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The sample will consist of children and adolescents (aged 6-18) referred to the Obesity Outpatient Clinic at Haukeland University Hospital by their general practitioner.
  • Criteria for admission to the clinic is an (IOTF) isoBMI of > 35, or a isoBMI > 30 with obesity related co-morbidity.
  • Both the child and at least one of the parents agrees to actively participate in the treatment.

Exclusion Criteria:

  • Severe somatic or psychiatric illness that makes adherence to the treatment program impossible.
  • Somatic conditions, syndromes or medications that lead to pathological weight gain.
  • Participation in other obesity treatment programs.

Sites / Locations

  • Haukeland University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Family-based behavioral social facilitation therapy.

Treatment as usual

Arm Description

The FBSFT condition includes 17 weekly family-based treatment sessions at the hospital obesity clinic followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital every third month for 2 years.The treatment targets both child and parent life-style; eating habits, physical activity, sedentary activity and sleep habits. Behavior modification techniques are systematically employed; such as self-monitoring, goal setting, reward systems, problem solving and stimulus control. In addition, FBSFT focuses on facilitating lifestyle change across different settings (family, friends, school and community) and harnessing social support for healthy habits, which is considered important for long-term weight control.

The TAU condition involves an assessment day with the multidisciplinary team (pediatrician, dietician, physical therapist and psychologist) at the hospital obesity clinic. Further a session with the nurse at the hospital clinic making a plan for behavioral lifestyle changes followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital clinic every third month for 12 months. After 12 months they will be offered treatment by family-based behavioral social facilitation therapy (as in the other treatment arm).

Outcomes

Primary Outcome Measures

Change in weight status, assessed as BMI, BMI standard deviation scores (SDSs) and percentages above the IOTF cut-off for overweight (%IOTF-25)
Height, weight will be measured by trained assessors at the Obesity Outpatient Clinic.

Secondary Outcome Measures

Change in waist circumference
Will be measured by trained assessors at the Obesity Outpatient Clinic
Change in %body fat assessed by Bio-impedance
Bio-impedance measurements of body composition will be conducted at the Obesity Outpatient Clinic using InBody 720.
Change in % body fat assessed by DXA
DXA-scans for determining the distribution of fat and muscle tissue will be conducted at the Department of Rheumathology at Haukeland University Hospital.
Change in Blood samples and cortisol measurements
Blood samples will be drawn in the morning after an overnight fast. Including measurements of total-cholesterol, HDL, LDL, TG, ASAT, ALAT, gamma-GT, bilirubin, creatinin, HbA1c and fasting insulin, c-peptide and glucose, TSH, fT4, CRP. Cortisol measurements from saliva and urine. A bio-bank for the storing and registering of biological materials is approved.
Change in blood pressure
Blood pressure will be measured by the pediatrician at the obesity clinic
Changes in eating habits - Food diary
The parents will be instructed to help their children to keep a diary of food and beverage intake for five days including two weekend days. They will use an electronic kitchen scale to weigh the food.
Changes in physical activity and sleep patterns - Accelerometers
Physical activity and sleep patterns will be measured by using accelerometers. Accelerometers are small devices that register movement. The accelerometers that will be used in this study are worn on the non-dominant wrist and resemble a watch. The accelerometers record all uni-axial movement over 0.05G in one-minute epochs
Changes in psychological parameters - The Child Behavior Checklist (CBCL)/Youth self-report (YSR)
The Child Behavior Checklist (CBCL) is a 138-item rating scale assessing behavioural and emotional symptoms in children that has both a child/youth and parent form.
Changes in psychological parameters - Children's Depression Inventory (CDI)
Children's Depression Inventory (CDI). CDI is a 27-item self-report test assessing the cognitive, affective and behavioural symptoms of depression in children (7-17 years).
Changes in psychological parameters - Self-Perception Profile for Children (SPPC).
Self-Perception Profile for Children (SPPC). SPPC is a self-report measure of self-perception or self-esteem in children aged 8 to 14 years and is widely used for research purposes. The questionnaire includes 36 statements and the children are asked to evaluate to which degree the statement fits their thoughts about themselves.
Changes in eating habits - The Dutch Eating Behavior Questionnaire Child version (DEBQ)
The Dutch Eating Behavior Questionnaire Child version (DEBQ) is a measure of disturbed eating patterns in children and youth (41). DEBQ consists of 3 sub-scales: emotional eating, external eating and restrained eating.
Changes in eating habits - The Youth Eating Disorder Examination-Questionnaire (YEDE-Q)
The Youth Eating Disorder Examination-Questionnaire (YEDE-Q) is a self-reported measure of eating patterns and eating disorder psychopathology. The YEDE-Q was designed to include measurements of binge eating in youth which have been poorly covered in other self-report measures of eating pathology.

Full Information

First Posted
February 21, 2014
Last Updated
September 20, 2021
Sponsor
University of Bergen
Collaborators
Haukeland University Hospital, Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02687516
Brief Title
Treatment of Severely Obese Children and Adolescents Employing "Family-based Behavioral Social Facilitation Treatment"
Official Title
Treatment of Severely Obese Children and Adolescents in Common Health Care Settings: An Effectiveness Study Employing "Family-based Behavioral Social Facilitation Treatment"
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
February 2014 (Actual)
Primary Completion Date
January 2021 (Actual)
Study Completion Date
May 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bergen
Collaborators
Haukeland University Hospital, Washington University School of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to evaluate the effectiveness of Family-based behavioral social facilitation therapy (FBSFT) in the treatment of severe obesity in children and adolescents compared to treatment as usual (TAU). The FBSFT condition includes 17 weekly family-based treatment sessions at the hospital obesity clinic followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital every third month for 2 years. The treatment targets both child and parent life-style; eating habits, physical activity, sedentary activity and sleep habits. Behavior modification techniques are employed; such as self-monitoring, goal setting, reward systems, problem solving and stimulus control. In addition, FBSFT focuses on facilitating lifestyle change across different settings (family, friends, school and community) and harnessing social support for healthy habits, which is considered important for long-term weight control. The TAU condition involves an assessment day with the multidisciplinary team (pediatrician, dietician, physical therapist and psychologist) at the hospital obesity clinic. Further a session with the nurse at the hospital clinic making a plan for behavioral lifestyle changes followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital clinic every third month for one year. SAMPLE AND STUDY DESIGN. The sample will consist of children and adolescents (aged 6-18) referred to the Obesity Outpatient Clinic at Haukeland University Hospital. Criteria for admission to the clinic is an (IOTF) isoBMI of > 35, or a isoBMI > 30 with obesity related co-morbidity. Based on current clinic data, estimations suggest that about 60 families of children with severe obesity will be referred to the Obesity Outpatient Clinic every year and be offered treatment. Recruitment will start in February 2014 and will continue in 2015 and 2016. After consenting to participation and completion of the initial assessments the families will be randomized to either FBSFT or treatment as usual (TAU). After one year the families randomized to TAU will be offered the FBSFT treatment. Measurement points for the most important outcome measures will be pre-treatment, post-treatment (at approximately 6 months), at 12 months, 18 months and 24 months. OUTCOME VARIABLES. Anthropometrical measures: Height, weight and waist-circumference, DXA-scans and bio-impedance measurements for determining the distribution of fat and muscle tissue. Physiological measures: Blood samples will be drawn in the morning after an overnight fast. Including measurements of total-cholesterol, HDL, LDL, TG, ASAT, ALAT, gamma-GT, bilirubin, creatinin, HbA1c and fasting insulin, c-peptide and glucose, TSH, fT4, CRP. Cortisol measurements from saliva and urine. Measurement of bloodpressure. Food records: The parents will be instructed to help their children to keep a diary of food and beverage intake for five days. They will use an electronic kitchen scale to weigh the food. Physical activity: Physical activity and sleep will be measured by using accelerometers. Psychological measures: The Child Behavior Checklist (CBCL) is a 138-item rating scale assessing behavioral and emotional symptoms in children/youth. Children's Depression Inventory (CDI). CDI is a 27-item self-report test assessing symptoms of depression in children (7-17 years). Self-Perception Profile for Children (SPPC). SPPC is a self-report measure of self-perception in children aged 8 to 14 years. The Dutch Eating Behavior Questionnaire Child version (DEBQ) is a measure of disturbed eating patterns in children and youth. The Youth Eating Disorder Examination-Questionnaire (YEDE-Q) is a self-reported measure of eating patterns and eating disorder psychopathology. OTHER MEASUREMENTS INCLUDED. The Parenting Scale (PS) is a 30-item questionnaire designed to measure different parental disciplines with children/youth. The scores on three sub-scales are calculated - Laxness, Overreactivity and Verbosity. The Barriers to Treatment Participation Scale (BTPS). The 44-item scale is developed and validated to address drop-out from treatment with out-patient psychological treatment of children and adolescents. Child and parent acceptability of the treatment will be measured by the FBSFT Acceptability Questionnaire. STUDY AIMS: To evaluate the effect of FBSFT compared to TAU for treatment of severe childhood and adolescent obesity in an ordinary health care setting on BMI, BMI SDS, body composition, cardio-metabolic health, eating habits, physical activity as well as psychological well-being. To identify predictors of treatment success and treatment drop-out with a focus on family variables and mental health. To evaluate treatment (FBSFT) implementation and treatment acceptability for children, parents and health care workers and experienced barriers to treatment, and how these factors influence children's and parents' treatment response.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Obesity
Keywords
Treatment, Child, Obesity, Behavioral treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Family-based behavioral social facilitation therapy.
Arm Type
Experimental
Arm Description
The FBSFT condition includes 17 weekly family-based treatment sessions at the hospital obesity clinic followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital every third month for 2 years.The treatment targets both child and parent life-style; eating habits, physical activity, sedentary activity and sleep habits. Behavior modification techniques are systematically employed; such as self-monitoring, goal setting, reward systems, problem solving and stimulus control. In addition, FBSFT focuses on facilitating lifestyle change across different settings (family, friends, school and community) and harnessing social support for healthy habits, which is considered important for long-term weight control.
Arm Title
Treatment as usual
Arm Type
Active Comparator
Arm Description
The TAU condition involves an assessment day with the multidisciplinary team (pediatrician, dietician, physical therapist and psychologist) at the hospital obesity clinic. Further a session with the nurse at the hospital clinic making a plan for behavioral lifestyle changes followed by monthly follow-up sessions with their local nurse and follow-up sessions at the hospital clinic every third month for 12 months. After 12 months they will be offered treatment by family-based behavioral social facilitation therapy (as in the other treatment arm).
Intervention Type
Behavioral
Intervention Name(s)
Family-based behavioral social facilitation therapy
Intervention Description
Family-based Behavioral Social Facilitation Treatment (FBSFT) is founded on the principles of standard family-based behavioural therapy for obesity. FBSFT targets life-style behaviors (diet, physical activity and sedentary activity) in a family setting. FBSFT includes some cognitive elements that are considered important in relation to behavioural change for instance problem solving and cognitive restructuring. FBSFT has an intensive treatment phase including weekly family meetings with therapists over 17 consecutive weeks. Further monthly or bi-weekly follow-up sessions with a focus on social facilitation and maintenance of healthy habits are recommended. The dietary guidance of FBSFT is based on the "Traffic light diet" in which foods are organized into GREEN, YELLOW and RED groups. Activity guidance of FBSFT uses the same system: GREEN activities have the highest intensity and should be engaged in most often, YELLOW activities sometimes, and RED activities.
Intervention Type
Behavioral
Intervention Name(s)
TAU - Treatment as usual
Intervention Description
This is the default treatment at the obesity clinic. After initial evaluation by paediatrician, nurse, nutritionist and physiotherapist, a "contract" is written including weight goal, nutritional plan and activity plan. Follow up monthly in primary Health care and every 3rd month at the obesity clinic.
Primary Outcome Measure Information:
Title
Change in weight status, assessed as BMI, BMI standard deviation scores (SDSs) and percentages above the IOTF cut-off for overweight (%IOTF-25)
Description
Height, weight will be measured by trained assessors at the Obesity Outpatient Clinic.
Time Frame
BMI will be measured at baseline and after 3, 6, 9, 12, 15, 18 and 24 months.
Secondary Outcome Measure Information:
Title
Change in waist circumference
Description
Will be measured by trained assessors at the Obesity Outpatient Clinic
Time Frame
Will be measured at baseline and after 3, 6, 9, 12, 15, 18 and 24 months.
Title
Change in %body fat assessed by Bio-impedance
Description
Bio-impedance measurements of body composition will be conducted at the Obesity Outpatient Clinic using InBody 720.
Time Frame
Measurements will be done at baseline, 6 months, 12 months, 18 months and 24 months
Title
Change in % body fat assessed by DXA
Description
DXA-scans for determining the distribution of fat and muscle tissue will be conducted at the Department of Rheumathology at Haukeland University Hospital.
Time Frame
Measurements will be made at baseline, at 6 months, at 12 months, at 18 months and at 24 months.
Title
Change in Blood samples and cortisol measurements
Description
Blood samples will be drawn in the morning after an overnight fast. Including measurements of total-cholesterol, HDL, LDL, TG, ASAT, ALAT, gamma-GT, bilirubin, creatinin, HbA1c and fasting insulin, c-peptide and glucose, TSH, fT4, CRP. Cortisol measurements from saliva and urine. A bio-bank for the storing and registering of biological materials is approved.
Time Frame
measurements will be done at baseline, 6 months, 12 months, 18 months and 24 months
Title
Change in blood pressure
Description
Blood pressure will be measured by the pediatrician at the obesity clinic
Time Frame
Will be measured at baseline, 6 months, 12 months, 18 months and 24 months
Title
Changes in eating habits - Food diary
Description
The parents will be instructed to help their children to keep a diary of food and beverage intake for five days including two weekend days. They will use an electronic kitchen scale to weigh the food.
Time Frame
Measurements will be obtained at baseline, 6 months, 12, months, 18 months and 24 months
Title
Changes in physical activity and sleep patterns - Accelerometers
Description
Physical activity and sleep patterns will be measured by using accelerometers. Accelerometers are small devices that register movement. The accelerometers that will be used in this study are worn on the non-dominant wrist and resemble a watch. The accelerometers record all uni-axial movement over 0.05G in one-minute epochs
Time Frame
Measurements will be made at baseline, 6 months, 12 months, 18 months and 24 months
Title
Changes in psychological parameters - The Child Behavior Checklist (CBCL)/Youth self-report (YSR)
Description
The Child Behavior Checklist (CBCL) is a 138-item rating scale assessing behavioural and emotional symptoms in children that has both a child/youth and parent form.
Time Frame
Measurements will be obtained at baseline, at 6 months, 12 months, 18 months and 24 months
Title
Changes in psychological parameters - Children's Depression Inventory (CDI)
Description
Children's Depression Inventory (CDI). CDI is a 27-item self-report test assessing the cognitive, affective and behavioural symptoms of depression in children (7-17 years).
Time Frame
Assessments at baseline, at 6 months, 12 months, 18 months and 24 months
Title
Changes in psychological parameters - Self-Perception Profile for Children (SPPC).
Description
Self-Perception Profile for Children (SPPC). SPPC is a self-report measure of self-perception or self-esteem in children aged 8 to 14 years and is widely used for research purposes. The questionnaire includes 36 statements and the children are asked to evaluate to which degree the statement fits their thoughts about themselves.
Time Frame
Assessments at baseline, at 6 months, 12 months, 18 months and 24 months
Title
Changes in eating habits - The Dutch Eating Behavior Questionnaire Child version (DEBQ)
Description
The Dutch Eating Behavior Questionnaire Child version (DEBQ) is a measure of disturbed eating patterns in children and youth (41). DEBQ consists of 3 sub-scales: emotional eating, external eating and restrained eating.
Time Frame
Assessments at baseline, at 6 months, 12 months, 18 months and 24 months
Title
Changes in eating habits - The Youth Eating Disorder Examination-Questionnaire (YEDE-Q)
Description
The Youth Eating Disorder Examination-Questionnaire (YEDE-Q) is a self-reported measure of eating patterns and eating disorder psychopathology. The YEDE-Q was designed to include measurements of binge eating in youth which have been poorly covered in other self-report measures of eating pathology.
Time Frame
Assessments at baseline, at 6 months, 12 months, 18 months and 24 months
Other Pre-specified Outcome Measures:
Title
The Parenting Scale (PS)
Description
The Parenting Scale (PS) is a 30-item questionnaire designed to measure different parental disciplines with children and youth. The scores on three sub-scales are calculated - Laxness, Overreactivity and Verbosity.
Time Frame
Assessment at baseline, 6 months, 12 months, 18 months and 24 months
Title
The Barriers to Treatment Participation Scale (BTPS).
Description
The Barriers to Treatment Participation Scale (BTPS). The 44-item scale is developed and validated to address drop-out from treatment with out-patient psychological treatment of children and adolescents. Scores are distributed across 4 sub-scales: (1) Stressors and obstacles that compete with treatment, (2) treatment demands and issues, (3) perceived relevance of the treatment, (4) therapeutic relationship.
Time Frame
Assessment at 4 months after enrollment or point of deciding to end treatment for the FBSFT arm
Title
FBSFT Acceptability Questionnaire.
Description
Child and parent acceptability of the treatment will be measured by the FBSFT Acceptability Questionnaire. The measure consists of two subscales: satisfaction and perceived utility. This measure has been informed by assessments used in a treatment study for pediatric obesity in the UK, which evaluates degree to which participants were pleased with the intervention and the extent to which they perceived components to be helpful
Time Frame
Measurement at 6 months after enrollment for the FBSFT arm

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The sample will consist of children and adolescents (aged 6-18) referred to the Obesity Outpatient Clinic at Haukeland University Hospital by their general practitioner. Criteria for admission to the clinic is an (IOTF) isoBMI of > 35, or a isoBMI > 30 with obesity related co-morbidity. Both the child and at least one of the parents agrees to actively participate in the treatment. Exclusion Criteria: Severe somatic or psychiatric illness that makes adherence to the treatment program impossible. Somatic conditions, syndromes or medications that lead to pathological weight gain. Participation in other obesity treatment programs.
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
ZIP/Postal Code
5020
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
27769209
Citation
Skjakodegard HF, Danielsen YS, Morken M, Linde SF, Kolko RP, Balantekin KN, Wilfley DE, Juliusson PB. Study Protocol: A randomized controlled trial evaluating the effect of family-based behavioral treatment of childhood and adolescent obesity-The FABO-study. BMC Public Health. 2016 Oct 21;16(1):1106. doi: 10.1186/s12889-016-3755-9.
Results Reference
derived

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Treatment of Severely Obese Children and Adolescents Employing "Family-based Behavioral Social Facilitation Treatment"

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