Trial of a Novel Family-Based Intervention to Increase Outdoor Time and Fitness (FIT)

National University of Singapore

Status and phase: Completed; Phase 3

Conditions: Myopia; Obesity

Treatments: Behavioral: Family-based Outdoor program

Study type: Interventional

Funder types: Other

Identifiers

NCT01388205

FIT-NUS-10-520

Details and patient eligibility

About

This study aims to implement a new family-based health behavior community program to increase time spent outdoors and physical activity among Singapore children aged 6 to 12 years in a 1-year randomized clinical trial. 300 children from 250 families will be randomly assigned to either a family-based intervention or no intervention. The family-based intervention comprises structured weekend outdoor activities organized by National Parks and incentives for children to wear a pedometer and increase their daily steps. Families who meet their monthly step and outdoor activity goals will receive a range of prizes and incentives. Both groups will receive brochures on the National Myopia Prevention Program and physical activity. The success of the intervention will be evaluated through light meters, 7-day outdoor diaries, questionnaires documenting outdoor time and myopia; as well as pedometer steps, walking tests, and body mass index. A community-based intervention will be developed to improve the health of Singapore children by increasing outdoor time and physical activity to prevent myopia and obesity.

Full description

To develop, implement, and evaluate a novel incentive-based family intervention to increase time spent outdoors and physical activity among children aged 6 to 12 years in a 1-year randomized controlled trial.

Enrollment: 285 patients

Sex: All

Ages: 6 to 12 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Children between 6 and 12 years of age with no known health problems preventing them from staying outdoors or walking for physical activity will be included as long as they are Singapore citizens or permanent residents.
• Both myopic and non-myopic children will be included

Exclusion criteria

• Children with medical conditions such as Type 1 diabetes, severe asthma, cancer or mental illness will be excluded.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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285 participants in 2 patient groups

Family-based Intervention Arm

Experimental group

Treatment:

Behavioral: Family-based Outdoor program

Control

No Intervention group