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IMplementation of the Family Support PRogramme A Healthy School Start to Prevent OVErweight and Obesity (IMPROVE) (IMPROVE)

Primary Purpose

Pediatric Obesity, Overnutrition, Child, Prediabetic State

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Healthy School Start
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pediatric Obesity focused on measuring BMI, Fidelity, Hybrid type 3 design, Health promotion, Implementation strategies, Primary health care, School health care, Nutrition

Eligibility Criteria

5 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All children and their parents at the included schools. All involved personnel at the included schools

Exclusion Criteria:

  • No

Sites / Locations

  • MunicipalityRecruiting
  • MunicipalityRecruiting
  • Municipality

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Basic

Enhanced

Arm Description

All schools will receive the HSS program. Schools randomly assigned to group 1 will receive implementation strategy bundle 1 (Basic).

All schools will receive the HSS program. Schools randomly assigned to group 2 will receive implementation strategy bundle 1+2 (Enhanced).

Outcomes

Primary Outcome Measures

Change in fidelity (A) assessed by questionnaire to parents and school staff
Adherence to the four HSS components by indicators developed for this study. Information will be gathered through attendance logs and questionnaires to school staff and parents.
Change in fidelity (R) assessed by questionnaire to parents
Responsiveness to the four HSS components by indicators developed for this study. Information will be gathered through questionnaires to parents.

Secondary Outcome Measures

Change in acceptability of the HSS program assessed by questionnaire
Feasibility of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Change in appropriateness of the HSS program measured by questionnaire
Appropriateness of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Change in feasibility of the HSS program measured by questionnaire
Feasibility of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Change in Organisational readiness of school principals assessed by questionnaire
Organisational readiness to change as perceived by school principals with the Leader Readiness to Implement Tool (LRIT)
Change in Organisational readiness by school staff assessed by questionnaire
Organisational readiness to change as perceived by school nurses and teachers with the Staff Readiness to Implement Tool (SRIT)
Fidelity to implementation strategies assessed by checklist
Assessment based on checklist developed for this study. Each strategy will be graded as 0=not implemented, 1=partially implemented, 2=fully implemented.
Change in child weight status assessed through measurement of height (m) and weight (kg)
Child BMI will be calculated as in kg/m^2. Weight status will be assessed using age-appropriate BMI cut-off values for thinness, overweight and obesity according to the International Obesity Task Force.
Change in child BMI z-score assessed through measurement of height (m) and weight (kg)
Child BMI will be calculated as in kg/m^2. The BMI z-score will be calculated according to a Swedish reference standard (Karlberg).
Change in child diet assessed by parent questionnaire
Dietary indicator foods (fruit, vegetables and energy-dense products) assessed by the diet portion of the Eating and Physical Activity Questionnaire (EPAQ)
Change in parental feeding practices assessed by parent questionnaire
Assessed with the Swedish short version of the Comprehensive Feeding Practices Questionnire (CFPQ)
Change in parents' risk of type 2 diabetes assessed by FINDRISC questionnaire
The FINDRISC self-evaluation test to calculate risk of developing type 2 diabetes on a scale from 0-26 points

Full Information

First Posted
July 12, 2021
Last Updated
October 4, 2023
Sponsor
Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT04984421
Brief Title
IMplementation of the Family Support PRogramme A Healthy School Start to Prevent OVErweight and Obesity (IMPROVE)
Acronym
IMPROVE
Official Title
IMplementation and Evaluation of the School-based Family Support PRogramme A Healthy School Start to Promote Child Health and Prevent OVErweight and Obesity (IMPROVE) - Study Protocol for a Cluster-randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet

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
IMPROVE is an implementation study aiming to explore the effects of two bundled implementation strategies on the intervention fidelity of the Healthy School Start program (primary outcome) while simultaneously monitoring effects on health outcomes of children and parents (secondary outcomes). Thirty schools in two municipalities will receive the HSS program reaching about 1400 families per school year, for two years.
Detailed Description
IMPROVE aims to conduct a hybrid type 3 evaluation design to test the effects of bundled implementation strategies on the intervention fidelity (primary outcome) of the Healthy School Start (HSS) program while simultaneously monitoring effects on health outcomes of children and parents (secondary outcomes). The HSS is a 4-component family support program for children starting school (5-7 years of age) promoting healthy dietary habits and physical activity in the home environment to prevent childhood obesity and parent risk of developing type 2 diabetes. IMPROVE is a cluster-randomized controlled trial with two arms to evaluate and compare the effects of two different bundles of implementation strategies on intervention fidelity expressed as adherence and responsiveness at 12 and 24 months. Thirty schools in two municipalities will participate in the study reaching about 1400 families per school year. In stakeholder workshops, key implementation determinants were identified according to the domains of the Consolidated Framework for Implementation Research. Through a consensus process with stakeholders, two bundles of implementation strategies were tailored to address context-specific determinants. Schools randomly assigned to group 1 will receive bundle 1 (Basic) and group 2 will receive bundle 1+2 (Enhanced), consisting mainly of external facilitation, fidelity monitoring and feedback strategies. Secondary outcomes will include acceptability, appropriateness, feasibility, organisational readiness as perceived by school staff, child weight status and diet, and parents' risk of type 2 diabetes. Linear and ordinal regression analysis will be used to test the effect on the primary and secondary outcomes, taking clustering into consideration where needed. Process evaluation will be conducted through key stakeholder interviews to investigate experiences of the program and stakeholder perceptions on sustainability. This systematic approach to investigating the effects of two different bundles of implementation strategies tailored to context-specific determinants on the fidelity of the HSS intervention will provide new insight into feasible implementation strategies and the external supports needed for a school-based health program like the HSS to be effective and sustainable. Results will help inform how to bridge the gap between the research on school-based health programs and routine practice in schools.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Obesity, Overnutrition, Child, Prediabetic State, Diabetes Mellitus, Type 2, Overweight, Childhood
Keywords
BMI, Fidelity, Hybrid type 3 design, Health promotion, Implementation strategies, Primary health care, School health care, Nutrition

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized controlled trial with a hybrid type 3 evaluation design
Masking
Participant
Masking Description
Researchers and school personnel will not be blinded to group allocation, but parents and children will be blinded.
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Basic
Arm Type
Active Comparator
Arm Description
All schools will receive the HSS program. Schools randomly assigned to group 1 will receive implementation strategy bundle 1 (Basic).
Arm Title
Enhanced
Arm Type
Experimental
Arm Description
All schools will receive the HSS program. Schools randomly assigned to group 2 will receive implementation strategy bundle 1+2 (Enhanced).
Intervention Type
Behavioral
Intervention Name(s)
Healthy School Start
Intervention Description
The Healthy School Start program is a universal 4-component family support program for children starting school (5-7 years of age) promoting healthy dietary habits and physical activity in the home environment to prevent childhood obesity and parents' risk of developing type 2 diabetes. It is targeting both children and parents.
Primary Outcome Measure Information:
Title
Change in fidelity (A) assessed by questionnaire to parents and school staff
Description
Adherence to the four HSS components by indicators developed for this study. Information will be gathered through attendance logs and questionnaires to school staff and parents.
Time Frame
Measured at 12 and 24 months
Title
Change in fidelity (R) assessed by questionnaire to parents
Description
Responsiveness to the four HSS components by indicators developed for this study. Information will be gathered through questionnaires to parents.
Time Frame
Measured at 12 and 24 months
Secondary Outcome Measure Information:
Title
Change in acceptability of the HSS program assessed by questionnaire
Description
Feasibility of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Time Frame
Measured at baseline, 12, 24, and 36 months
Title
Change in appropriateness of the HSS program measured by questionnaire
Description
Appropriateness of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Time Frame
Measured at baseline, 12, 24, and 36 months
Title
Change in feasibility of the HSS program measured by questionnaire
Description
Feasibility of implementing the intervention as perceived by school staff, measured with the questionnaire developed by Weiner et al.
Time Frame
Measured at baseline, 12, 24, and 36 months
Title
Change in Organisational readiness of school principals assessed by questionnaire
Description
Organisational readiness to change as perceived by school principals with the Leader Readiness to Implement Tool (LRIT)
Time Frame
Measured at baseline, 12, 24, and 36 months
Title
Change in Organisational readiness by school staff assessed by questionnaire
Description
Organisational readiness to change as perceived by school nurses and teachers with the Staff Readiness to Implement Tool (SRIT)
Time Frame
Measured at baseline, 12, 24, and 36 months
Title
Fidelity to implementation strategies assessed by checklist
Description
Assessment based on checklist developed for this study. Each strategy will be graded as 0=not implemented, 1=partially implemented, 2=fully implemented.
Time Frame
May each year
Title
Change in child weight status assessed through measurement of height (m) and weight (kg)
Description
Child BMI will be calculated as in kg/m^2. Weight status will be assessed using age-appropriate BMI cut-off values for thinness, overweight and obesity according to the International Obesity Task Force.
Time Frame
Measured at baseline and after 24 months
Title
Change in child BMI z-score assessed through measurement of height (m) and weight (kg)
Description
Child BMI will be calculated as in kg/m^2. The BMI z-score will be calculated according to a Swedish reference standard (Karlberg).
Time Frame
Measured at baseline and after 24 months
Title
Change in child diet assessed by parent questionnaire
Description
Dietary indicator foods (fruit, vegetables and energy-dense products) assessed by the diet portion of the Eating and Physical Activity Questionnaire (EPAQ)
Time Frame
Baseline, 12 months, and 24 months
Title
Change in parental feeding practices assessed by parent questionnaire
Description
Assessed with the Swedish short version of the Comprehensive Feeding Practices Questionnire (CFPQ)
Time Frame
Baseline, 12 months, and 24 months
Title
Change in parents' risk of type 2 diabetes assessed by FINDRISC questionnaire
Description
The FINDRISC self-evaluation test to calculate risk of developing type 2 diabetes on a scale from 0-26 points
Time Frame
Measured at Baseline, 12 months, and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All children and their parents at the included schools. All involved personnel at the included schools Exclusion Criteria: No
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kristi S Annerstedt, PhD
Phone
(0)70-9202081
Ext
+46
Email
kristi.sidney@ki.se
First Name & Middle Initial & Last Name or Official Title & Degree
Liselotte S Elinder, PhD
Phone
(0)72-526 69 91
Ext
+46
Email
liselotte.schafer-elinder@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liselotte S Elinder, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Municipality
City
Huddinge
State/Province
Stockholm Region
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christina D Andersson, BSc
Email
Christina.Dolke-Andersson@huddinge.se
First Name & Middle Initial & Last Name & Degree
Barbro Lönnkvist, BSc
Email
barbro.lonnkvist@huddinge.se
Facility Name
Municipality
City
Sigtuna
State/Province
Stockholm Region
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kerstin Alksten, MSc
Email
kerstin.alksten@sigtuna.se
First Name & Middle Initial & Last Name & Degree
Birgitta Asplund
Email
birgitta.asplund@sigtuna.se
Facility Name
Municipality
City
Södertälje
State/Province
Stockholm Region
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jenny Stanser, BSc
Email
jenny.stanser@sodertalje.se
First Name & Middle Initial & Last Name & Degree
Anna Appelgren, BSc
Email
anna.appelgren@sodertalje.se

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34488691
Citation
Elinder LS, Wiklund CA, Norman A, Stattin NS, Andermo S, Patterson E, Hemmingsson E, Cook C, Raposo S, Kwak L. IMplementation and evaluation of the school-based family support PRogram a Healthy School Start to promote child health and prevent OVErweight and obesity (IMPROVE) - study protocol for a cluster-randomized trial. BMC Public Health. 2021 Sep 6;21(1):1630. doi: 10.1186/s12889-021-11663-2.
Results Reference
derived
Links:
URL
https://ki.se/gph/en-frisk-skolstart
Description
Project website

Learn more about this trial

IMplementation of the Family Support PRogramme A Healthy School Start to Prevent OVErweight and Obesity (IMPROVE)

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