- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00961740
Childhood Obesity- Characteristics and Treatment
Cognitive Behavioural Treatment for Childhood Obesity- A Clinical Trial.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Aim of the study: Evaluating a manualized treatment program for childhood obesity.
Participants: 49 families with children with obesity, aged 8-12. The participants will be recruited through referrals from medical doctors or nurses in primary health care or through ads in newspapers. Inclusion criteria: age between 8 and 12 and satisfying the criteria for obesity according to Coles indexes for BMI for the given gender and age group (Cole et al, 2000). Exclusion criteria are cardiovascular disease, diabetes and severe psychopathology. Before inclusion the child will go through a medical examination by a pediatrician as well as an interview by a psychologist.
Procedure/treatment program: The manualized treatment is based on principles from cognitive behavioural therapy and is family based. The treatment consists of 14 sessions (60 minutes), where a clinical psychologist meet the family together. The first 12 sessions are given at a weekly basis, the last two sessions are administered half a year and one year after the more intensive part of the treatment. The treatment program includes elements such as: 1) general overview of the treatment plan, 2) basic information about nutrition, physical activity and metabolism, 3) keeping a food and activity diary, 4) a behavioral modification plan aimed at changing habits such as watching TV, video and PC causing sedentary behavior, 5) a behavioral modification plan aimed at changing eating patterns and level of physical activity 6) a module consisting of identifying and avoiding risk factors associated with unhealthy and/or excessive eating and sedentary behavior, 7) a module focusing upon parent counseling 8)modules focusing on problem solving skills, reactions in stressful situations and automatic thoughts 9) modules discussing bullying and self-esteem 10)home work assignments between sessions(Barlow & Dietz, 1998; Zametkin et al, 2004). In all, 20 subjects will be randomized to immediate treatment (12 weeks) while the other half of the subjects will randomized to a waiting-list control group. The waiting-list control group will receive treatment.
Instruments measuring the results of the treatment:
Behavioural change: Daily logs on activity and nutrition will be kept by the subjects for one week prior to and one week following the intensive phase of the treatment (12-sessions), as well as after one year. In the same periods actigraphs will be used in order to obtain objective data on physical activity levels.
Self-report measures: The Self-Perception Profile for Children (SPPC) (Harter, 1985)is a well recognized self-report measure that assesses general and dimensional (cognitive, social, and physical) self-esteem in children and adolescents. The Children's Depression Inventory (CDI) a commonly used screening device for pediatric depression containing a 27-item, symptom-oriented scale (Kovacs, 1985). Child Behavior Check-list (CBCL,a well recognized parent-report measure, measuring children's social competence and behavioral problems(Achenbach,1991).
Physiological measures: Fasting plasma insulin, glucose and triglyceride, cholesterol (total, HDL, LDL), HbA1c and lipoprotein A.
Physical measures: Weight, BMI, waist circumference, blood pressure. All measures will be administered pre-treatment (and pre-wait-list for the control group), after 12-sessions of treatment and after one year.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hordaland
-
Bergen, Hordaland, Norway, 5020
- University of Bergen
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- obese status, according to Cole et al.'s (2000) international criteria.
Exclusion Criteria:
- serious somatic or metal health problems
- diabetes
- cardiovascular disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
OTHER: Cognitive Behavioral Therapy
Design: 49 children (aged 8-12)with obesity was recruited, the children were randomly assigned to a group that started a cognitive behavioural intervention immediately after recruitment, and another group that received the same treatment after a 12-week wait list condition.
For further description of the treatment, see summary.
Arm 1 (this arm) started receiving a cognitive behavioural intervention immediately after randomization.
|
See summary
See Summary
Other Names:
|
|
OTHER: 12-weeks waitlist condition
After an initial pre-assessment no contact were made before assessment after 12-weeks and start of intervention after this assessment.
After the 12-week waitlist condition the families were offered the same familibased cognitive behavioral intervention as in arm one.
|
See summary
See Summary
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Body Mass Index
Time Frame: (pre-treatment), 4-months after starting treatment, 12-months after ending intensive phase of treatment
|
(pre-treatment), 4-months after starting treatment, 12-months after ending intensive phase of treatment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Self-perception Profile for Children (Harter, 1985)
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Waist circumference
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Child Behavior Checklist (CBCL)
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Children's Depression Inventory (CDI) (Kovacs)
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Physical activity actigraphy and self-report
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Food diary
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
|
Blood measures (cholesterol, triglyceride, insulin, glucose, HbA1c, lipoprotein A)
Time Frame: (pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
(pre-treatment), 4 months after starting treatment, 12 months after ending intensive phase of treatment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yngvild S Danielsen, University of Bergen
Publications and helpful links
General Publications
- Barlow SE; Expert Committee. Expert committee recommendations regarding the prevention, assessment, and treatment of child and adolescent overweight and obesity: summary report. Pediatrics. 2007 Dec;120 Suppl 4:S164-92. doi: 10.1542/peds.2007-2329C.
- Kovacs M. The Children's Depression, Inventory (CDI). Psychopharmacol Bull. 1985;21(4):995-8. No abstract available.
- Achenbach, T. M. Integrative Guide to the 1991 CBCL/4-18, YSR, and TRF Profiles. Burlington, VT: University of Vermont, Department of Psychology 1991.
- Cole TJ, Bellizzi MC, Flegal KM, Dietz WH. Establishing a standard definition for child overweight and obesity worldwide: international survey. BMJ. 2000 May 6;320(7244):1240-3. doi: 10.1136/bmj.320.7244.1240.
- Harter, S. Manual for the self-perception profile for children. Denver, CO: University of Denver, 1985.
- Zametkin AJ, Zoon CK, Klein HW, Munson S. Psychiatric aspects of child and adolescent obesity: a review of the past 10 years. J Am Acad Child Adolesc Psychiatry. 2004 Feb;43(2):134-50. doi: 10.1097/00004583-200402000-00008.
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 911180- Helse Vest
- 15792- NSD
- 241.06-REK Vest
- 1244-Biobankregisteret, ShDir
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.