MedPath

A city-wide program to encourage active and sustainable travel in young people

Not Applicable
Conditions
Active and sustainable travel in young people
Not Applicable
Registration Number
ISRCTN17633761
Lead Sponsor
South Eastern Finland University of Applied Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
300
Inclusion Criteria

1. 13 - 15-year-old young people who attend classes in the study schools
2. Give informed consent and have their guardian's consent to participate
3. Additionally, from amongst the participants, a sample of 12 to 15 young people with diverse travel habits and 2 to 4 parents will be recruited for the semi-structured interviews

Exclusion Criteria

Does not meet inclusion criteria

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of moderate-to-vigorous physical activity (hours/day). Participants will use a validated Fibion® device (Fibion Inc., Jyväskylä, Finland) for 8 days, 24 hours a day at baseline, 4 months and 8 months. The Fibion® device is attached to the participant's right thigh with a waterproof cover and medical tape to measure sitting and various forms of physical activity, including cycling.
Secondary Outcome Measures
NameTimeMethod
1. Active travel practices as a duration of different modes of transportation per week: walking, walking to the stop, cycling, cycling to the stop, personal motorized vehicle, bus, and car, assessed at baseline, 4 months and 8 months. Based on geographical information, the duration of trips is estimated using a map based PPGIS (Public Participatory GIS) survey, where participants indicate the mode of transportation, departure, and destination for each trip. In the PPGIS survey, participants are asked if they use the bus daily, several times a week, once or twice a week (weekly bus users), less than weekly, or never (less than weekly bus users)<br>2. Sitting time (accelerometer attached to thigh, Fibion device) assessed at baseline, 4 months and 8 months
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