Skip to main content
Clinical Trials/NCT02637752
NCT02637752
Completed
N/A

Efficacy of Nutrition and Physical Activity Counselling for Pre-adolescent Children in a Dental Setting: A Randomized Clinical Trial

University of Toronto0 sites168 target enrollmentSeptember 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Childhood Obesity
Sponsor
University of Toronto
Enrollment
168
Primary Endpoint
Body Mass Index (BMI)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Background: Childhood obesity imposes a great burden on the healthcare system. Given the increased frequency of dental compared to medical visits during childhood, dentists may be in an ideal position to recognize patients at risk of developing obesity. This randomized clinical trial explored the efficacy of a brief nutrition and physical activity counseling for healthy weight 6 to11 year-old children in a university-based pediatric dental clinic.

Methods: 168 children, 6-11 year old, were allocated to test and control groups and their Body Mass index (BMI) were recorded. Their parents/caregivers completed a questionnaire regarding their child's nutrition, physical activity and screen time. The parents/caregivers of the test group then received a brief counseling session that encouraged an increase in children's physical activity, and a decrease in sugar-sweetened beverages and screen time. Data, collected at baseline and follow-up session (within 6-12 months) were analyzed using general linear regression, adjusting for age, gender, socio-demographic characteristics, education, labour force, income and awareness of school nutrition policy (P≤ 0.05).

Registry
clinicaltrials.gov
Start Date
September 2011
End Date
April 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amir Azarpazhooh

Dr.

University of Toronto

Eligibility Criteria

Inclusion Criteria

  • 6 to 11 years old

Exclusion Criteria

  • Younger or older children
  • those with systemic diseases (such as diabetes, cardiac problems, dyslipidemia, elevated cholesterol, obstructive sleep apnea, stroke, fatty liver disease, osteoarthritis, orthopedic problems and any forms of cancer)
  • Children and their accompanying parents or caregivers (hereafter, caregivers) unable to communicate in English
  • if caregivers were unreachable after three attempts by phone

Outcomes

Primary Outcomes

Body Mass Index (BMI)

Time Frame: 6-12 months from the baseline

Secondary Outcomes

  • physical activity (hrs/day)(6-12 months)
  • screen time (hrs/day)(6-12 months)
  • number of sugar-sweetened beverages consumed per day(6-12 months)

Similar Trials