Actively Recruiting
Health4Life a Digital Intervention to Promote Healthy Lifestyle Behaviours From the Start of Life
Led by Karolinska Institutet · Updated on 2025-08-27
504
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
Sponsors
K
Karolinska Institutet
Lead Sponsor
F
Forte
Collaborating Sponsor
AI-Summary
What this Trial Is About
The overall aim of this project is to evaluate the effectiveness and implementation of a digital intervention to support parents to create healthy lifestyle behaviours from the start of their infant's life, in order to prevent overweight and obesity. Using a randomized controlled trial with a hybrid type I implementation-effectiveness design we will: 1. evaluate the effectiveness of the 16-month Health4Life intervention on: 1. Children's' dietary intake, screen time, physical activity, and sleep 2. Children's body mass index (BMI) z-scores 3. Parental self-efficacy 2. Evaluate the cost-effectiveness of the Health4Life app. 3. Evaluate and explore the implementation of the Health4Life app within primary child healthcare with regards to its: 1. acceptability, appropriateness, and feasibility according to child healthcare nurses. 2. satisfaction and usage by parents.
CONDITIONS
Official Title
Health4Life a Digital Intervention to Promote Healthy Lifestyle Behaviours From the Start of Life
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infants aged 0 to 2 months attending routine visits at selected child healthcare centers in Sweden
You will not qualify if you...
- Infants diagnosed with a neurological or endocrine disorder
- Infants with a parent suffering from a serious physical or psychological disease that makes participation too demanding for the family
- Infants from families unable to understand the content of the app
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Karolinska Institutet
Huddinge, Sweden, 141 83
Actively Recruiting
Research Team
C
Christine Delisle Nyström, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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