Effectiveness of a Web-based, Computer-tailored, Pedometer-based Physical Activity Intervention for Adults: a Cluster-randomized Controlled Trial

Overview

The present study used a cluster-randomized controlled trial to evaluate the effects of a computer-tailored, pedometer-based Physical Activity (PA) intervention delivered through the Internet. An invitation e-mail with study information was sent to managers of 18 white-collar workplaces. Eight workplaces consented to participate. All employees of a single workplace were allocated at random to either the intervention or a waiting list control group, in order to avoid contamination between employees receiving the intervention and those who were not receiving the intervention. Subsequently, employees of the participating workplaces were recruited by e-mail. Only Dutch speaking employees between 18 and 65 years old, who had access to the Internet at work or at home, were eligible. Interested employees could sign up by returning a confirmation e-mail to the researchers. On receiving this information, a meeting was organized in each of the eight worksites to deliver all documents for baseline measurement (T0) to the participants, including an informed consent form, a blinded pedometer, an activity log and a self-administered questionnaire. During this meeting, information was provided on how to use the pedometer, how to log PA activities and how to answer the questionnaire. Moreover, the participants were asked to adhere to their usual PA pattern throughout the baseline measurement. After one week, all measurement tools were collected, and average daily step counts were calculated. At this point, participants in the intervention condition received (1) a booklet with information on how to increase steps, (2) a non-blinded pedometer, which they could use for three months, and (3) a username, a password and the amount of average daily steps, calculated by the researchers, so that participants could use this number when requesting the online computer-tailored step advice. Participants in the control condition did not receive any of the above mentioned intervention components. One and three months later, all participants again received a blinded pedometer, which was worn for one week. When wearing the blinded-pedometer one month (T1) and three months (T2) post baseline, intervention participants were allowed to also were the non-blinded pedometer. Furthermore, the same self-reported questionnaire was used to measure PA level at T1 and T2 in order to test the effectiveness of the intervention.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Health Services Research
    • Masking: None (Open Label)
  • Study Primary Completion Date: February 2013

Interventions

  • Behavioral: Physical Activity advice.
    • Subjects receive advice regarding physical activities.

Arms, Groups and Cohorts

  • No Intervention: Control group without advice
    • Control group receives no intervention or physical activity advice.
  • Experimental: Computer-tailored physical activity advice
    • Subjects receive computer-tailored physical activity advice.

Clinical Trial Outcome Measures

Primary Measures

  • Amount of physical activity at baseline.
    • Time Frame: at baseline
    • Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.
  • Amount of Physical activity 1 month after baseline.
    • Time Frame: 1 month after baseline
    • Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.
  • Amount of physical activity 3 months after baseline.
    • Time Frame: 3 months after baseline
    • Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.

Secondary Measures

  • Sedentary behaviour at baseline.
    • Time Frame: at baseline
    • International Physical Activity Questionnaire (IPAQ)
  • Sedentary behaviour 1 month after baseline.
    • Time Frame: 1 month after baseline
    • International Physical Activity Questionnaire (IPAQ)
  • Sedentary behaviour 3 months after baseline.
    • Time Frame: 3 months after baseline
    • International Physical Activity Questionnaire (IPAQ)

Participating in This Clinical Trial

Inclusion Criteria

  • Dutch speaking – Age range: 18 – 65 years old – Access to the Internet at work or at home

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 65 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • University Ghent
  • Collaborator
    • Research Foundation Flanders
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Ilse De Bourdeaudhuij, PhD, Principal Investigator, University Ghent

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.