Skip to main content
Clinical Trials/NCT02638675
NCT02638675
Completed
Not Applicable

Examining Financial Health Incentives to Promote Physical Activity Among Inactive Hospital Employees: A Web-based Randomized Control Trial

University of Toronto1 site in 1 country99 target enrollmentFebruary 6, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physically Inactive Hospital Employees
Sponsor
University of Toronto
Enrollment
99
Locations
1
Primary Endpoint
Steps
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The objective of this randomized control trial is to examine whether incentives-for-steps (i.e. $1 per day step count goals are reached) increase daily step counts among physically inactive hospital employees.

Detailed Description

A 24-week, parallel arm, randomized control trial will be employed to examine the impact of incentives on physical activity among physically inactive Hamilton Health Science Corporation employees. Participants will be randomly allocated (1:1) into control (i.e. wellness program and accelerometer) or intervention groups (i.e. wellness program, accelerometer, incentives), where only intervention participants will receive reward points for completing daily step count goals. After randomization, a baseline 'run-in' assessment phase will occur one week prior to the study intervention (T0). During this 'run-in' period, participants will wear a Bluetooth enabled StepsCount Piezo accelerometer, which will track participants' daily steps and moderate to vigorous physical activity (MVPA), and synchronize their accelerometer (i.e. upload information) to the Change4Life program for seven days. Participants will also be asked to complete the Behavioural Regulation to Exercise Questionnaire (BREQ-3) and the Self-Efficacy for Exercise Scale. Throughout the 24-week study, all participants will be asked to wear the accelerometer and synchronize it to the Change4Life program daily. Date, steps per day, and bout minutes of MVPA per day (bouts include 10 or more continuous minutes of MVPA) will be collected when the accelerometer is synchronized. Daily synchronization from the accelerometer to the Change4Life program must be completed by 10 am the next morning. Participants will be instructed to increase their daily step counts by 1,000 and 2,000 steps above baseline (T0) over the course of the first six weeks of the study. On week 7, participants will be asked to increase daily steps per day to 3,000 over baseline, and maintain that level of activity for the duration of the study. Outcome measures will be assessed at baseline (T0), intervention end point (T2), and follow up (T3).

Registry
clinicaltrials.gov
Start Date
February 6, 2017
End Date
November 30, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Guy Faulkner

Professor

University of Toronto

Eligibility Criteria

Inclusion Criteria

  • Over the age of 18 years
  • English speaking

Exclusion Criteria

  • Existing medical condition, which could be exacerbated by physical activity as measured by the Physical Activity Readiness Questionnaire.
  • Note. Participants cannot enrol in the study without Internet access

Outcomes

Primary Outcomes

Steps

Time Frame: Daily for 24 weeks

Steps per day will be objectively assessed using the Bluetooth enabled, medical grade, StepsCount Piezo accelerometer

Secondary Outcomes

  • Motivation to Exercise - Behavioural Regulation to Exercise Questionnaire; BREQ-3(Baseline (T0; week 0), intervention end point (T2; week 12), and follow up assessments (T3; week 24).)
  • 10 Minute Bouts of Moderate to Vigorous Physical Activity(Intervention end point (T2; week 12), and follow up assessments (T3; week 24).)
  • Walking Self-Efficacy - Self-Efficacy for Exercise Scale; SEE Scale(Baseline (T0; week 0), intervention end point (T2; week 12), and follow up assessments (T3; week 24).)

Study Sites (1)

Loading locations...

Similar Trials