Overweight and Obesity in Preschoolers (MLEurope)
Primary Purpose
Obesity, Overweight
Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Parent group
mHealth component
Standard care
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Children, Obesity, Treatment, Family, mHealth
Eligibility Criteria
Inclusion Criteria:
- 2 to 6 year old children with overweight or obesity according to international cut-offs.
- Children who have no other underlying medical condition(s).
- Parent(s) who have the ability to communicate in Swedish (for the Swedish part), Romanian (for the Romanian part), and Spanish (for the Spanish part).
Exclusion Criteria:
- Parent(s) not owning a smartphone compatible with the MINISTOP app.
Sites / Locations
- University of Medicine and Pharmacy "Victor Babes"
- University of the Balearic Islands & CIBEROBN
- Karolinska Instituet
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Parent group & mHealth component
Standard care
Arm Description
The intervention in the present study is a 10 week parent training group session (More and Less Program) followed by a 6-month mobile phone based intervention. Both components aim to develop healthy lifestyle behaviours regarding dietary habits and physical activity in 2-6 year olds. The intervention is delivered towards the parents.
Standard care for overweight and obesity
Outcomes
Primary Outcome Measures
Change in body mass index (BMI) z-score.
It is the most commonly used indicator of changes in weight status in pediatric obesity studies and enable comparison between other studies. The children's weight and height will be measured using standardized procedures and BMI z-scores will be derived from Swedish age and gender specific reference values.
Secondary Outcome Measures
Waist circumference
Measured at the mid-point between the lower rib and iliac crest.
Eating behaviour
Measured using the Child Eating Behaviour Questionnaire (CEBQ). It includes 35 items on eating styles comprising eight factors related to obesity risk. Parents rate each behavior on a five-point Likert scale. It is a 5-point response scale (''never, rarely, sometimes, mostly, always'' for Items 1-13, and ''disagree, slightly disagree, neutral, slightly agree, agree'' for items 14-49). Mean scores for each subscale will be calculated.
Parenting behaviour
Measured using the Comprehensive Feeding Practices Questionnaire (CFPQ). The CFPQ is a parent-report instrument, designed to measure feeding practices of parents of 2-to-8- year-old children. It contains 49 items comprising 12 factors: 'Encourage Balance and Variety', 'Environment', 'Involvement', 'Modeling', 'Monitoring', 'Teaching about Nutrition', 'Emotion Regulation', 'Food as Reward', 'Pressure', 'Child Control', 'Restriction for Health' and 'Restriction for Weight Control'.
Physical activity and sedentary behaviour
Assessed over 7 consecutive days using the ActiGraph wGT3x-BT accelerometer. Children will wear the ActiGraph on the non-dominant wrist 24hrs per day. Parents/caregivers will record when the device has been taken on and off and the activities performed during that time as well as when the child went to bed and woke up. The recorded movements will be used to estimate time in various activity levels (e.g., sedentary behavior, light physical activity etc.) by means of cut-offs.
Food intake
First void urinary sample from the child will be collected to assess child food intake. Urine samples will be assessed by proton nuclear magnetic resonance (1H-NMR) spectroscopy. Diet-discriminatory metabolites will be identified so that urine metabolite models can be developed and validated against 24 hour recall data and a food diary for children that attend preschool.
Epigenetic and metabolic markers
Fasting blood samples will be collected to assess reversibility of metabolic markers through epigenetic markers and the role of gut hormones. The epigenetic analysis will be carried out in white blood cells, which will required DNA extraction, bisulphite transformation and analysis with specific PCRs or other technologies involving hypothesis-driven CpGs. The unit of measurement/criteria will be changes in percentage of methylation (CpGs). These measurements will be related to other measurements, i.e.: metabolomics and anthropometric measurements. With all the measurements (anthropometrical, and biochemical/genomics) the final purpose would be to build a predictive score of changes related to weight status.
Feasibility, attrition, and acceptability of the intervention as assessed using semi-structured interviews with parents and health care professionals
In this qualitative assesment using semi-structured interviews we will thoroughly assess facilitators and barriers of recruitment as well as attrition to the intervention and feasibility and acceptability of the care offered. Both parents and health care professionals will be interviewed by trained staff in the research group post intervention. The interviews are recorded and fully transcribed before they are coded and analyzed using thematic analysis.
Full Information
NCT ID
NCT03800823
First Posted
January 2, 2019
Last Updated
October 5, 2023
Sponsor
Karolinska Institutet
Collaborators
University of Medicine and Pharmacy "Victor Babes" Timisoara, El Centro de Investigación Biomédica en Red, CIBER
1. Study Identification
Unique Protocol Identification Number
NCT03800823
Brief Title
Overweight and Obesity in Preschoolers
Acronym
MLEurope
Official Title
A Randomized Controlled Trial for Overweight and Obesity in Preschoolers - The More and Less Study Europe
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 15, 2019 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
University of Medicine and Pharmacy "Victor Babes" Timisoara, El Centro de Investigación Biomédica en Red, CIBER
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
Obesity interventions in early childhood are recommended as they have been proven to be more effective than interventions later in life. The overall aim of this study is to assess the effectiveness, feasibility, and acceptance of an overweight and obesity intervention in socially disadvantaged families. Participants will be families with children aged 2-6 years (n = 300) with overweight or obesity and will be recruited from three sites: Stockholm, Sweden (n = 100); Timisoara, Romania (n = 100); and Mallorca, Spain (n = 100).
Detailed Description
The proposed randomized controlled trial has five specific aims:
Specific Aim 1: To determine the effectiveness of a 10 week parent-only group support program focusing on evidence-based parenting practices followed by a mobile health (mHealth) component for 6-months (n = 150) compared to standard care (n = 150) for overweight and obesity in pre-school children (change in BMI z-scores after 9 months primary outcome).
Specific Aim 2: To determine if the intervention can improve body composition (waist circumference), child eating behaviour, physical activity, and parental feeding practices in comparison to the control group.
Specific Aim 3: To assess reversibility of the molecular signatures of obesity following the intervention through epigenetic markers in white blood cells (methylation) and analyzing the role of the gut hormones.
Specific Aim 4: To assess and validate child food intake with metabolic markers in urine.
Specific Aim 5: To evaluate the feasibility of recruitment (facilitators and barriers), attrition and acceptability, as well as patient and caregiver satisfaction to the intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Overweight
Keywords
Children, Obesity, Treatment, Family, mHealth
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Parent group & mHealth component
Arm Type
Experimental
Arm Description
The intervention in the present study is a 10 week parent training group session (More and Less Program) followed by a 6-month mobile phone based intervention. Both components aim to develop healthy lifestyle behaviours regarding dietary habits and physical activity in 2-6 year olds. The intervention is delivered towards the parents.
Arm Title
Standard care
Arm Type
Active Comparator
Arm Description
Standard care for overweight and obesity
Intervention Type
Behavioral
Intervention Name(s)
Parent group
Intervention Description
In group sessions parents will learn how to use positive parenting practices (e.g., encouragement and limit setting) instead of ineffective practices (e.g., coercive behaviour, negative reciprocity). Using a parent group approach, each of the 10 sessions consist of introduction to effective parenting practices followed by a discussion and practice using role play and home practice assignments.
Intervention Type
Behavioral
Intervention Name(s)
mHealth component
Intervention Description
After the group sessions, parents will receive a 6-month mHealth program (MINISTOP app) based on social cognitive theory with strategies to change unhealthy diet/physical activity behaviours. The program includes information, advice, and strategies to change unhealthy behaviours and the possibility to register the child's intake of fruit, vegetables, candy, sweetened beverages, and sedentary time.
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
Standard care for overweight and obesity.
Primary Outcome Measure Information:
Title
Change in body mass index (BMI) z-score.
Description
It is the most commonly used indicator of changes in weight status in pediatric obesity studies and enable comparison between other studies. The children's weight and height will be measured using standardized procedures and BMI z-scores will be derived from Swedish age and gender specific reference values.
Time Frame
Baseline, 10 weeks, 9 months, 15 months, 21 months
Secondary Outcome Measure Information:
Title
Waist circumference
Description
Measured at the mid-point between the lower rib and iliac crest.
Time Frame
Baseline, 10 weeks, 9 months, 15 months, 21 months
Title
Eating behaviour
Description
Measured using the Child Eating Behaviour Questionnaire (CEBQ). It includes 35 items on eating styles comprising eight factors related to obesity risk. Parents rate each behavior on a five-point Likert scale. It is a 5-point response scale (''never, rarely, sometimes, mostly, always'' for Items 1-13, and ''disagree, slightly disagree, neutral, slightly agree, agree'' for items 14-49). Mean scores for each subscale will be calculated.
Time Frame
Baseline, 9 months, 15 months, 21 months
Title
Parenting behaviour
Description
Measured using the Comprehensive Feeding Practices Questionnaire (CFPQ). The CFPQ is a parent-report instrument, designed to measure feeding practices of parents of 2-to-8- year-old children. It contains 49 items comprising 12 factors: 'Encourage Balance and Variety', 'Environment', 'Involvement', 'Modeling', 'Monitoring', 'Teaching about Nutrition', 'Emotion Regulation', 'Food as Reward', 'Pressure', 'Child Control', 'Restriction for Health' and 'Restriction for Weight Control'.
Time Frame
Baseline, 9 months, 15 months, 21 months
Title
Physical activity and sedentary behaviour
Description
Assessed over 7 consecutive days using the ActiGraph wGT3x-BT accelerometer. Children will wear the ActiGraph on the non-dominant wrist 24hrs per day. Parents/caregivers will record when the device has been taken on and off and the activities performed during that time as well as when the child went to bed and woke up. The recorded movements will be used to estimate time in various activity levels (e.g., sedentary behavior, light physical activity etc.) by means of cut-offs.
Time Frame
Baseline, 9 months
Title
Food intake
Description
First void urinary sample from the child will be collected to assess child food intake. Urine samples will be assessed by proton nuclear magnetic resonance (1H-NMR) spectroscopy. Diet-discriminatory metabolites will be identified so that urine metabolite models can be developed and validated against 24 hour recall data and a food diary for children that attend preschool.
Time Frame
Baseline, 9 months
Title
Epigenetic and metabolic markers
Description
Fasting blood samples will be collected to assess reversibility of metabolic markers through epigenetic markers and the role of gut hormones. The epigenetic analysis will be carried out in white blood cells, which will required DNA extraction, bisulphite transformation and analysis with specific PCRs or other technologies involving hypothesis-driven CpGs. The unit of measurement/criteria will be changes in percentage of methylation (CpGs). These measurements will be related to other measurements, i.e.: metabolomics and anthropometric measurements. With all the measurements (anthropometrical, and biochemical/genomics) the final purpose would be to build a predictive score of changes related to weight status.
Time Frame
Baseline, 9 months
Title
Feasibility, attrition, and acceptability of the intervention as assessed using semi-structured interviews with parents and health care professionals
Description
In this qualitative assesment using semi-structured interviews we will thoroughly assess facilitators and barriers of recruitment as well as attrition to the intervention and feasibility and acceptability of the care offered. Both parents and health care professionals will be interviewed by trained staff in the research group post intervention. The interviews are recorded and fully transcribed before they are coded and analyzed using thematic analysis.
Time Frame
Baseline, 4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
2 to 6 year old children with overweight or obesity according to international cut-offs.
Children who have no other underlying medical condition(s).
Parent(s) who have the ability to communicate in Swedish (for the Swedish part), Romanian (for the Romanian part), and Spanish (for the Spanish part).
Exclusion Criteria:
Parent(s) not owning a smartphone compatible with the MINISTOP app.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paulina Nowicka
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Medicine and Pharmacy "Victor Babes"
City
Timişoara
ZIP/Postal Code
30041
Country
Romania
Facility Name
University of the Balearic Islands & CIBEROBN
City
Palma De Mallorca
ZIP/Postal Code
07122
Country
Spain
Facility Name
Karolinska Instituet
City
Huddinge
ZIP/Postal Code
14157
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
35962359
Citation
Eli K, Neovius C, Nordin K, Brissman M, Ek A. Parents' experiences following conversations about their young child's weight in the primary health care setting: a study within the STOP project. BMC Public Health. 2022 Aug 12;22(1):1540. doi: 10.1186/s12889-022-13803-8.
Results Reference
derived
PubMed Identifier
34336760
Citation
Serban CL, Putnoky S, Ek A, Eli K, Nowicka P, Chirita-Emandi A. Making Childhood Obesity a Priority: A Qualitative Study of Healthcare Professionals' Perspectives on Facilitating Communication and Improving Treatment. Front Public Health. 2021 Jul 15;9:652491. doi: 10.3389/fpubh.2021.652491. eCollection 2021.
Results Reference
derived
PubMed Identifier
31706318
Citation
Sjunnestrand M, Nordin K, Eli K, Nowicka P, Ek A. Planting a seed - child health care nurses' perceptions of speaking to parents about overweight and obesity: a qualitative study within the STOP project. BMC Public Health. 2019 Nov 9;19(1):1494. doi: 10.1186/s12889-019-7852-4.
Results Reference
derived
PubMed Identifier
31307412
Citation
Ek A, Delisle Nystrom C, Chirita-Emandi A, Tur JA, Nordin K, Bouzas C, Argelich E, Martinez JA, Frost G, Garcia-Perez I, Saez M, Paul C, Lof M, Nowicka P. A randomized controlled trial for overweight and obesity in preschoolers: the More and Less Europe study - an intervention within the STOP project. BMC Public Health. 2019 Jul 15;19(1):945. doi: 10.1186/s12889-019-7161-y.
Results Reference
derived
Learn more about this trial
Overweight and Obesity in Preschoolers
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