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Holbæk Obesity Treatment (HOT) Versus Conventional Obesity Treatment (COT) in Children With Overweight or Obesity. (HOT vs COT)

Primary Purpose

Childhood Overweight and Obesity

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Holbæk Obesity Treatment
Conventional Obesity Treatment
Sponsored by
Holbaek Sygehus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Childhood Overweight and Obesity

Eligibility Criteria

6 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Overweight or obesity defined as BMI corresponding to or above the 90th percentile for age and sex (International Obesity Task Force cut-offs).
  • Age six to < 12 years at enrolment.
  • Signed informed consent from both parents or legal guardians.

Exclusion Criteria:

  • Participation in multidisciplinary obesity treatment (i.e. treatment involving more than one type of healthcare profession) within the past 12 months.
  • Having a sibling already enrolled in the HOT versus COT trial.
  • Both parents or legal guardians unable to communicate in Danish (written or oral).
  • Child unable to communicate in Danish (oral).
  • Current or previous clinical diagnosis of either anorexia or bulimia according to ICD-10.

Sites / Locations

  • Municipality health center, GuldborgsundRecruiting
  • Municipality heath center, BallerupRecruiting
  • Municipality health center, Frederikssund KommuneRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HOT

COT

Arm Description

Holbæk Obesity Treatment

Conventional Obesity Treatment

Outcomes

Primary Outcome Measures

BMI SDS
BMI SDS assessed according to the International Obesity Task Force cut-offs.
Quality of life (PedsQL)
Quality of life assessed by Pediatric Quality of Life Inventory (PedsQL)

Secondary Outcome Measures

Full Information

First Posted
September 7, 2021
Last Updated
April 12, 2023
Sponsor
Holbaek Sygehus
Collaborators
Copenhagen Trial Unit, Center for Clinical Intervention Research, University of Copenhagen, Statens Serum Institut, University of Florida, Leeds Beckett University, University of Minnesota, Hebrew University of Jerusalem, Frederiksberg University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05038683
Brief Title
Holbæk Obesity Treatment (HOT) Versus Conventional Obesity Treatment (COT) in Children With Overweight or Obesity.
Acronym
HOT vs COT
Official Title
Holbæk Obesity Treatment (HOT) Versus Conventional Obesity Treatment (COT) in Children With Overweight or Obesity. An Investigator-initiated, Multi-center, Randomized, Parallel Group, Clinical Superiority Trial With Blinded Outcome Assessment. HOT Versus COT Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 26, 2022 (Actual)
Primary Completion Date
January 2025 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Holbaek Sygehus
Collaborators
Copenhagen Trial Unit, Center for Clinical Intervention Research, University of Copenhagen, Statens Serum Institut, University of Florida, Leeds Beckett University, University of Minnesota, Hebrew University of Jerusalem, Frederiksberg University Hospital

4. Oversight

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

5. Study Description

Brief Summary
The HOT versus COT trial aims to compare the effectiveness of two different lifestyle interventions for treatment of childhood overweight and obesity with the purpose of informing future clinical practice guidelines within this field. The aim is to conduct this investigation in an optimal trial design with the lowest possible risk of bias.
Detailed Description
Obesity is a chronic, progressive, and severe disease that compromises growth, development, and the general health and well-being of children, adolescents, and adults all around the globe. Current treatment within this field varies considerably, but the prevailing concept is that treatment should be lifelong with a focus on implementing and maintaining changes regarding diet, physical activity, sedentary behavior, sleep, etc. The Holbæk Obesity Treatment (HOT) is built on the understanding that obesity is a complex chronic disease regulated by a neuroendocrine system, where weight-reducing actions initiate counteractive mechanisms to defend fat mass. Conventional obesity treatment (COT) is based on a view that obesity results from energy imbalances and focuses on motivation, few changes at a time, and a narrative approach towards healthy energy intake and physical activity. These two approaches represent fundamentally different treatments of overweight and obesity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Overweight and Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Due to the nature of the interventions, it will not be possible to blind the healthcare providers administering the interventions. We will attempt to blind the participants by not informing them about which intervention group we consider experimental and which group we consider control. However, the participants included in HOT will be governed by a digital solution where Dr. Holm will be identifiable and thus revealing the HOT. In all other aspects of the trial, we will employ blinding, incl. outcome assessment. Statisticians, and investigators drawing conclusions will be fully blinded. We will conduct the statistical analyses with the intervention groups coded as eg. 'A' and 'B'. The steering committee will write two abstracts while the blinding is intact; one assuming the experimental intervention group is 'A' and the control intervention group is 'B', and one assuming the opposite. After these two abstracts have both obtained consensus, the code will be broken.
Allocation
Randomized
Enrollment
554 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HOT
Arm Type
Experimental
Arm Description
Holbæk Obesity Treatment
Arm Title
COT
Arm Type
Active Comparator
Arm Description
Conventional Obesity Treatment
Intervention Type
Behavioral
Intervention Name(s)
Holbæk Obesity Treatment
Intervention Description
Obesity is a chronic, progressive, severe, recidivistic, and complex disease, which mandates that children and adolescents with overweight or obesity have access to a professional medical healthcare service as other pediatric chronic diseases, implying a lifelong course of treatment. The HOT method is further based on the physiological insight into the endocrine regulation of fat mass; especially on how the body adapts when it is challenged by weight loss. These insights include an understanding where the body shifts into an energy-preserving mode when the individual is initiating weight-reducing actions, such as a reduced caloric intake or an increased level of physical activity, which has numerous impacts on communication and pedagogy. HOT is administered by healthcare nurses and dietitians at healthcare centers in Danish municipalities. Each treatment will be conducted as face-to-face sessions totalling a range of six to 12 hours for 12 months.
Intervention Type
Behavioral
Intervention Name(s)
Conventional Obesity Treatment
Intervention Description
Obesity is viewed as a chronic disease that is ultimately thought to result from an imbalance between energy intake and energy expenditure. However, multiple factors, both environmental and genetic, are thought to influence the disease as well. As obesity reflects energy imbalances, the treatment plan should be designed to induce a slightly negative energy balance by focusing on diet, physical activity, and inactivity through behavior change. Taking one step at a time, will in the end lead to the same energy balance result (i.e. weight loss) and will be more sustainable for the participant whose motivation is absolutely pivotal in this process. COT is administered by healthcare nurses and dietitians at healthcare centers in Danish municipalities. Each treatment will be conducted as face-to-face sessions totalling a range of six to 12 hours for 12 months.
Primary Outcome Measure Information:
Title
BMI SDS
Description
BMI SDS assessed according to the International Obesity Task Force cut-offs.
Time Frame
End of intervention (12 months)
Title
Quality of life (PedsQL)
Description
Quality of life assessed by Pediatric Quality of Life Inventory (PedsQL)
Time Frame
End of intervention (12 months)
Other Pre-specified Outcome Measures:
Title
Symptoms of depression and anxiety
Description
Symptoms of depression and anxiety assessed with the questionnaire RCADS.
Time Frame
End of intervention (12 months)
Title
Serious adverse events (SAE)
Description
Proportion of participants with one or more SAEs defined as any adverse event that results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, or results in persistent or significant disability or incapacity.
Time Frame
End of intervention (12 months)
Title
Anorexia or bulimia
Description
Proportion of participants with a clinical diagnosis of anorexia or bulimia
Time Frame
End of intervention (12 months)
Title
School absence
Description
Number of days absent from kindergarten and school (excluding holidays).
Time Frame
End of intervention (12 months)
Title
Body composition
Description
Body composition, defined as % body fat by using bioelectrical impedance analysis (BIA)
Time Frame
End of intervention (12 months)
Title
Waist circumference
Description
Waist circumference
Time Frame
End of intervention (12 months)
Title
Systolic blood pressure
Description
Systolic blood pressure
Time Frame
End of intervention (12 months)
Title
Diastolic blood pressure
Description
Diastolic blood pressure
Time Frame
End of intervention (12 months)
Title
Serum leptin
Description
Concentrations of serum leptin
Time Frame
End of intervention (12 months)
Title
Total cholesterol
Description
Concentrations of serum total cholesterol
Time Frame
End of intervention (12 months)
Title
Low density lipoprotein (LDL)
Description
Concentrations of serum low density lipoprotein (LDL) cholesterol
Time Frame
End of intervention (12 months)
Title
Triglycerides
Description
Concentrations of serum triglycerides
Time Frame
End of intervention (12 months)
Title
Insulin
Description
Concentrations of serum insulin
Time Frame
End of intervention (12 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Overweight or obesity defined as BMI corresponding to or above the 90th percentile for age and sex (International Obesity Task Force cut-offs). Age six to < 12 years at enrolment. Signed informed consent from both parents or legal guardians. Exclusion Criteria: Participation in multidisciplinary obesity treatment (i.e. treatment involving more than one type of healthcare profession) within the past 12 months. Having a sibling already enrolled in the HOT versus COT trial. Both parents or legal guardians unable to communicate in Danish (written or oral). Child unable to communicate in Danish (oral). Current or previous clinical diagnosis of either anorexia or bulimia according to ICD-10.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jens-Christian Holm, Ph.d., MD
Phone
+4559484192
Email
jhom@regionsjaelland.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jens-Christian Holm, Ph.d., MD
Organizational Affiliation
The Children's Obesity Clinic, Department of Pediatrics, Holbæk Hospital, Part of Copenhagen University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Municipality health center, Guldborgsund
City
Nykøbing Falster
State/Province
Guldborgsund
ZIP/Postal Code
4800
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hanne Ryttesgaard, RN
Facility Name
Municipality heath center, Ballerup
City
Ballerup
ZIP/Postal Code
2750
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lotte Stentz, RN
Facility Name
Municipality health center, Frederikssund Kommune
City
Frederikssund
ZIP/Postal Code
3600
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bodil M Gjøl, RN

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Yes

Learn more about this trial

Holbæk Obesity Treatment (HOT) Versus Conventional Obesity Treatment (COT) in Children With Overweight or Obesity.

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