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Clinical Trials/NCT02871830
NCT02871830CompletedNot Applicable

Effects of a Peer-led Walking In ScHools Intervention on Physical Activity Levels of Adolescent Girls: a School-based Cluster Randomised Controlled Trial

University of Ulster0 sites200 target enrollmentStarted: January 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
200
Primary Endpoint
Total daily physical activity

Study Overview

Brief Summary

Children and young people are recommended to undertake at least 60 minutes of moderate to vigorous intensity physical activity each day. However recent findings have indicated that only 51% of children aged 7 years were meeting these guidelines. Previous research has also highlighted girls are significantly less active than. Furthermore, children living in Northern Ireland are least likely to meet the guidelines, with only 43.4% of children here reaching the recommended ≥ 60 minutes a day. The development of interventions which can successfully increase levels of physical activity in adolescent girls in Northern Ireland is of key importance. The aim of this intervention is to investigate whether or not girls (aged 11-13 years) can increase their daily levels of physical activity over a 12 week period by taking part in a school-based brisk walking intervention. The impact of participating in a school-based brisk walking intervention on a range of other outcome measures will also be investigated. A total sample of 200 adolescent females will be recruited onto the study, with recruitment of participants taking place at the school level. Following written consent from parents/guardians and assent from participants, participants will be randomised at the school level to either participate in the walking intervention or to act as controls. Objective physical activity will be assessed at 3 time points using an Actigraph accelerometer. At baseline, post-intervention (12 weeks) and follow up (4 months post-intervention) participants will also undergo measurements of height, weight, waist and hip circumference, bloody pressure, and cardiorespiratory fitness. Participants will also complete questionnaires assessing levels of physical activity and a number of psychosocial variables at each time point. Following completion of follow up measurements, a sub-sample of participants (n=45) will be invited to take part in focus groups to evaluate their experiences of the intervention.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
11 Years to 13 Years (Child)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • 11-13 years old
  • Attend a school selected to take part in the study
  • Healthy and free from any medical condition that limits their participation in a brisk walking intervention, for example, a musculoskeletal injury

Exclusion Criteria

  • Male pupils
  • Those who are unable to walk or for whom walking is contraindicated will not be eligible for inclusion

Outcomes

Primary Outcomes

Total daily physical activity

Time Frame: Change between baseline and post-intervention (12 weeks) and 4-months post-intervention

Measured for 7 consecutive days using Actigraph accelerometer at each time-point

Secondary Outcomes

  • Self-efficacy for walking(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Waist hip ratio(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Physical activity intensity(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Cardiorespiratory fitness(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Self-efficacy for physical activity(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Social support for physical activity and walking(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Self-reported physical activity(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Weight(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Blood pressure(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)
  • Attitude to exercise(Change between baseline and post-intervention (12 weeks) and 4-months post-intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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