Guelph Family Health Study: Full Study

NCT ID: NCT02939261

Last Updated: 2018-09-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

900 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-06-01

Study Completion Date

2020-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The overall objective of this research is to test, among families with children age 2-5 years, the immediate and longer-term impacts of a home-based intervention to improve household routines associated with reduced obesity risk. The investigators primary hypothesis is that, compared to control, children in the intervention group will have lower BMI following the 6-month intervention period and 18-month follow-up period. The secondary outcomes are change in children's % body fat, waist circumference and obesity-related behaviours: sleep, activity, sedentary behaviour, family meals, and dietary intake. Although child outcomes are the focus of this evaluation, changing household routines may also improve parent behaviour; thus, the investigators will assess change in parent behaviours and weight outcomes. This study will also assess the cost-effectiveness of the intervention from a societal perspective.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The overall objective of this research is to test, among families with children age 2-5 years, the immediate and longer-term impacts of a home-based intervention to improve household routines associated with reduced obesity risk. The primary hypothesis is that, compared to control, children in the intervention group will have lower BMI following the 6-month intervention period and 18-month follow-up period. The secondary outcomes are change in children's % body fat, waist circumference and obesity-related behaviours: sleep, activity, sedentary behaviour, family meals, and dietary intake. Although child outcomes are the focus of this evaluation, changing household routines may also improve parent behaviour; thus, the investigators will assess change in parent behaviours and weight outcomes. This study also assess the cost-effectiveness of the intervention from a societal perspective.

The investigators will randomly allocate 356 socio-economically diverse Ontario families to receive either: 1) 4 motivational coaching home visits, bi-weekly emails, and mailed behaviour supports (intervention group), or 2) Monthly emails with general health information (control group). Primary and secondary outcomes will be assessed at baseline, post-intervention (6-months), and 18-month follow-up, and data will be analyzed by intention to treat.

This study tests a novel and promising approach to obesity prevention - an approach that engages families at home, where they eat, play, and sleep. The interdisciplinary investigator team has partnered with parents and key knowledge users in public health and primary care to develop this intervention. As a result, this research could provide a sustainable model for early life obesity prevention, leading to long-term improvements in health and reduction in costs to the health system and society as a whole.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obesity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control

Families randomized to control will receive monthly emails containing publicly available handouts on general child health.

Group Type ACTIVE_COMPARATOR

Control

Intervention Type BEHAVIORAL

monthly emails with general health information

Intervention - 4 Home Visits

Families randomized to the intervention will receive: a) 4 home visits from a health educator, b) weekly e-mails, and c) monthly mailed behavioural supports.

Group Type EXPERIMENTAL

Intervention - 4 Home Visits

Intervention Type BEHAVIORAL

4 home visits from a health educator, weekly e-mails, and monthly mailed behavioural supports.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Intervention - 4 Home Visits

4 home visits from a health educator, weekly e-mails, and monthly mailed behavioural supports.

Intervention Type BEHAVIORAL

Control

monthly emails with general health information

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* families who have at least 1 child age 18 months - 5 years
* families who live in the Guelph area
* families who can respond to English surveys

Exclusion Criteria

* plan to move away within the next year
* have children with severe health conditions (e.g., cerebral palsy) that prevent participation in study activities.
Minimum Eligible Age

18 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Guelph

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Jess Haines

Associate Professor/GFHS Associate Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jess Haines, PhD

Role: PRINCIPAL_INVESTIGATOR

Unviersity of Guelph

David Ma, PhD

Role: STUDY_DIRECTOR

University of Guelph

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Univeristy of Guelph

Guelph, Ontario, Canada

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Canada

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Jess Haines, PhD

Role: CONTACT

519-824-4120 ext. 53780

Angela Annis, MSc

Role: CONTACT

519-824-4120 ext. 56168

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Jess Haines, PhD

Role: primary

519-824-4120 ext. 53780

Angela Annis, MSc

Role: backup

519-824-4120 ext. 56168

References

Explore related publications, articles, or registry entries linked to this study.

Jacob R, Buchholz AC, Darlington G, Duncan AM, Vallis LA, Chaput JP, Annis A, Nixon M, Irwin JD, Morrow D, Ma DWL, Haines J. Impact of a Home-Based Obesity Prevention Intervention on Children's and Parents' BMI: Findings From the Guelph Family Health Study Randomised Controlled Trial. Pediatr Obes. 2025 Oct 22:e70062. doi: 10.1111/ijpo.70062. Online ahead of print.

Reference Type DERIVED
PMID: 41125536 (View on PubMed)

Ribey SCS, Coyle-Asbil HJ, Osojnicki K, Coyle-Asbil B, Vallis LA, Darlington G, Duncan AM, Ma DWL, Haines J, Buchholz AC. Associations between objectively measured nighttime sleep duration, sleep timing, and sleep quality and body composition in toddlers in the Guelph Family Health Study. Appl Physiol Nutr Metab. 2025 Jan 1;50:1-7. doi: 10.1139/apnm-2024-0244. Epub 2024 Nov 20.

Reference Type DERIVED
PMID: 39566036 (View on PubMed)

Yu J, Mahajan A, Darlington G, Buchholz AC, Duncan AM, Haines J, Ma DWL; Guelph Family Health Study. Free sugar intake from snacks and beverages in Canadian preschool- and toddler-aged children: a cross-sectional study. BMC Nutr. 2023 Mar 8;9(1):44. doi: 10.1186/s40795-023-00702-3.

Reference Type DERIVED
PMID: 36890595 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

14AP009

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Families and Schools for Health
NCT02659319 COMPLETED NA
Obesity Prevention for Pre-Adolescents
NCT00185978 COMPLETED PHASE2
The Healthy Families Project
NCT01193374 COMPLETED NA