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The More & Less Study: A Trial Testing Different Treatment Approaches to Obesity in Preschoolers (M&L)

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Parent training group
Standard treatment with focus on lifestyle
Parent training group with booster sessions
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring children, obesity, treatment, family

Eligibility Criteria

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

Inclusion Criteria:

  • age 4-6 years old
  • obesity as defined by international cut-offs (Cole T. J. et al. BMJ, 2000).

Exclusion Criteria:

  • weight affecting diseases

Sites / Locations

  • Karolinska Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Treatment focus - Parenting vs lifestyle

Length of treatment

Arm Description

To determine the effectiveness of two obesity treatment interventions: 1) parent training group (n=90) and 2) standard treatment with focus on lifestyle (n=90). The two treatment conditions will be evaluated with respect to child weight status (BMI SDS; primary outcome), psychosocial and metabolic health, lifestyle choices, and family functioning (secondary outcomes). This design will allow us to assess whether a program targeting only parents and focusing on parenting practices will result in better outcomes than treatment as usual emphasizing lifestyle changes.

To understand the influence of treatment duration by comparing the effectiveness of two obesity treatment interventions: the parent training group administered for 12 wks only (n=45) and the parent training group with booster sessions which include additional booster sessions at 8-week intervals for the following year (n=45). Thus we will randomize families to either a group with booster sessions or without. This design will allow us to evaluate if prolonged care is necessary to maintain intervention effects, or if a 12-week program is equally effective.

Outcomes

Primary Outcome Measures

Change in Body Mass Index (BMI) SDS
Measurements of children's weight and height

Secondary Outcome Measures

Change in parenting practices, general and specific
Measured with validated questionnaires such as Child Feeding Questionnaire, Child Eating Behaviour Questionnaire and Lifestyle Behaviour Checklist. Parent's general parenting will be assessed with a questionnaire specifically developed for this study.
Change in child's dietary intake and behaviour
Measured using validated questionnaires such as Child Eating Behaviour Questionnaire and Food Frequency Questionnaire.
Change in child's physical activity
With questions about child's physical activity and screen time using Lifestyle Behaviour Checklist.
Change in family functioning
Using a validated questionnaire Family Assessment Device (FAD).
Change in child's metabolic health
Assessed by measurements of children's blood pressure, lipids, fasting glucose, insulin, and homeostasis model of insulin resistance. All these measurements are routinely assessed in all children with obesity in Stockholm. Blood tests are not required to participate in the study.
Change in parent's functioning
Measured by a validated questionnaire, the Beck Depression Inventory.
Waist circumference
Measured in children and parents
Change in child's functioning
Measured with a validated questionnaire, the Child Behaviour Checklist.
Change in socioeconomic status
With a questionnaire developed for this study based on routine assessments at the Child Health Care and a questionnaire used at the Oregon Social Learning Center (OSLC) for similar population (families with young children).

Full Information

First Posted
February 12, 2013
Last Updated
October 5, 2023
Sponsor
Karolinska Institutet
Collaborators
Oregon Social Learning Center
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1. Study Identification

Unique Protocol Identification Number
NCT01792531
Brief Title
The More & Less Study: A Trial Testing Different Treatment Approaches to Obesity in Preschoolers
Acronym
M&L
Official Title
The More & Less Study: A Randomized Controlled Trial Testing Different Treatment Approaches to Obesity in Preschoolers
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
January 2013 (Actual)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
December 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Oregon Social Learning Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Obesity has been shown to be resistant to treatment in adults, adolescents, and in school age children, but not during early childhood. Yet knowledge on the effectiveness of early childhood treatment programs for obesity is still very limited, preventing the widespread implementation of such programs. The overarching purpose of this study is to evaluate the effectiveness of early treatment of childhood obesity. The investigators plan to perform a carefully-designed randomized controlled trial that will evaluate different treatment options offered to families with children with obesity, organized within the healthcare system and followed up for at least 1 year post-baseline. Participants will be children aged 4-6 years (N=180) with obesity and their parents. This study will facilitate a close examination of key treatment components and mechanisms of change. Results from this study will lead to better healthcare options for obesity treatment during childhood and ultimately to the prevention of obesity later in life from a public health perspective.
Detailed Description
The proposed randomized controlled trial has four specific aims: Specific Aim #1: PARENTING OR LIFESTYLE? To determine the effectiveness of two obesity treatment conditions: 1) parent training (n=90) and 2) treatment as usual focused on lifestyle changes (n=90). The two treatment conditions will be evaluated with respect to child weight status (BMI SDS; primary outcome), psychosocial and metabolic health, lifestyle choices, and family functioning (secondary outcomes). Specific Aim #2: OPTIMAL LENGTH OF TREATMENT AND FOLLOW-UP? To understand the influence of treatment duration we will compare the effectiveness of the parent training program administered for 10 wks only and for 10 wks plus additional booster sessions at 8-week intervals for the following year. All groups will be followed up for at least one year post-baseline. Specific Aim #3: TO START AT AGE 4,5 OR 6? To assess the influence of child age at the start of treatment on the treatment outcomes. Specific Aim #4: MEDIATORS AND MODERATORS? To determine whether changes in targeted parenting skills (such as limit setting, monitoring and problem-solving) will mediate child obesity outcomes by examining all treatment groups. In addition, we will examine moderators of intervention effects (e.g. socioeconomic status (SES), parental weight status, and depression).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
children, obesity, treatment, family

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Treatment focus - Parenting vs lifestyle
Arm Type
Experimental
Arm Description
To determine the effectiveness of two obesity treatment interventions: 1) parent training group (n=90) and 2) standard treatment with focus on lifestyle (n=90). The two treatment conditions will be evaluated with respect to child weight status (BMI SDS; primary outcome), psychosocial and metabolic health, lifestyle choices, and family functioning (secondary outcomes). This design will allow us to assess whether a program targeting only parents and focusing on parenting practices will result in better outcomes than treatment as usual emphasizing lifestyle changes.
Arm Title
Length of treatment
Arm Type
Experimental
Arm Description
To understand the influence of treatment duration by comparing the effectiveness of two obesity treatment interventions: the parent training group administered for 12 wks only (n=45) and the parent training group with booster sessions which include additional booster sessions at 8-week intervals for the following year (n=45). Thus we will randomize families to either a group with booster sessions or without. This design will allow us to evaluate if prolonged care is necessary to maintain intervention effects, or if a 12-week program is equally effective.
Intervention Type
Behavioral
Intervention Name(s)
Parent training group
Intervention Description
The More & Less group will focus on how to use positive parenting practices (e.g., reinforcement/encouragement, limit setting, monitoring, problem-solving, positive involvement, and emotion regulation) instead of ineffective practices (e.g., coercive behavior, negative reciprocity, escalation, and negative reinforcement). Using a parent-group approach to intervention administration, each of the twelve More & Less sessions (1.5h/wk) consist of introduction to effective parenting practices followed by a discussion and practice using role play and home practice assignments. The information and procedures will be tailored to focus on changes in the home environment, mostly related to child food habits and physical activity.
Intervention Type
Behavioral
Intervention Name(s)
Standard treatment with focus on lifestyle
Intervention Description
The treatment will be provided by local pediatricians in outpatient pediatric departments and will be based on lifestyle modifications, as recommended in the action plan for Stockholm County.
Intervention Type
Behavioral
Intervention Name(s)
Parent training group with booster sessions
Intervention Description
Parent training group with additional booster sessions at 8-week intervals for the following year.
Primary Outcome Measure Information:
Title
Change in Body Mass Index (BMI) SDS
Description
Measurements of children's weight and height
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in parenting practices, general and specific
Description
Measured with validated questionnaires such as Child Feeding Questionnaire, Child Eating Behaviour Questionnaire and Lifestyle Behaviour Checklist. Parent's general parenting will be assessed with a questionnaire specifically developed for this study.
Time Frame
1 year
Title
Change in child's dietary intake and behaviour
Description
Measured using validated questionnaires such as Child Eating Behaviour Questionnaire and Food Frequency Questionnaire.
Time Frame
1 year
Title
Change in child's physical activity
Description
With questions about child's physical activity and screen time using Lifestyle Behaviour Checklist.
Time Frame
1 year
Title
Change in family functioning
Description
Using a validated questionnaire Family Assessment Device (FAD).
Time Frame
1 year
Title
Change in child's metabolic health
Description
Assessed by measurements of children's blood pressure, lipids, fasting glucose, insulin, and homeostasis model of insulin resistance. All these measurements are routinely assessed in all children with obesity in Stockholm. Blood tests are not required to participate in the study.
Time Frame
1 year
Title
Change in parent's functioning
Description
Measured by a validated questionnaire, the Beck Depression Inventory.
Time Frame
1 year
Title
Waist circumference
Description
Measured in children and parents
Time Frame
Baseline, 3 months, 1 year
Title
Change in child's functioning
Description
Measured with a validated questionnaire, the Child Behaviour Checklist.
Time Frame
1 year
Title
Change in socioeconomic status
Description
With a questionnaire developed for this study based on routine assessments at the Child Health Care and a questionnaire used at the Oregon Social Learning Center (OSLC) for similar population (families with young children).
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 4-6 years old obesity as defined by international cut-offs (Cole T. J. et al. BMJ, 2000). Exclusion Criteria: weight affecting diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paulina Nowicka, Ph.D.
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institute
City
Stockholm
ZIP/Postal Code
141 57
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31481062
Citation
Sandvik P, Ek A, Eli K, Somaraki M, Bottai M, Nowicka P. Picky eating in an obesity intervention for preschool-aged children - what role does it play, and does the measurement instrument matter? Int J Behav Nutr Phys Act. 2019 Sep 3;16(1):76. doi: 10.1186/s12966-019-0845-y.
Results Reference
derived
PubMed Identifier
31300528
Citation
Ek A, Lewis Chamberlain K, Sorjonen K, Hammar U, Etminan Malek M, Sandvik P, Somaraki M, Nyman J, Lindberg L, Nordin K, Ejderhamn J, Fisher PA, Chamberlain P, Marcus C, Nowicka P. A Parent Treatment Program for Preschoolers With Obesity: A Randomized Controlled Trial. Pediatrics. 2019 Aug;144(2):e20183457. doi: 10.1542/peds.2018-3457. Epub 2019 Jul 12.
Results Reference
derived
PubMed Identifier
26231850
Citation
Ek A, Chamberlain KL, Ejderhamn J, Fisher PA, Marcus C, Chamberlain P, Nowicka P. The More and Less Study: a randomized controlled trial testing different approaches to treat obesity in preschoolers. BMC Public Health. 2015 Aug 1;15:735. doi: 10.1186/s12889-015-1912-1.
Results Reference
derived

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The More & Less Study: A Trial Testing Different Treatment Approaches to Obesity in Preschoolers

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