Effectiveness of a Web-based, Computer-tailored, Pedometer-based Physical Activity Intervention for Adults: a Cluster-randomized Controlled Trial
1 other identifier
interventional
274
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2012
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2013
CompletedFirst Submitted
Initial submission to the registry
March 4, 2014
CompletedFirst Posted
Study publicly available on registry
March 6, 2014
CompletedMarch 6, 2014
March 1, 2014
9 months
March 4, 2014
March 5, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Amount of physical activity at baseline.
Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.
at baseline
Amount of Physical activity 1 month after baseline.
Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.
1 month after baseline
Amount of physical activity 3 months after baseline.
Using International Physical Activity Questionnaire (IPAQ) and Omron HJ-203-ED pedometer.
3 months after baseline
Secondary Outcomes (3)
Sedentary behaviour at baseline.
at baseline
Sedentary behaviour 1 month after baseline.
1 month after baseline
Sedentary behaviour 3 months after baseline.
3 months after baseline
Study Arms (2)
Control group without advice
NO INTERVENTIONControl group receives no intervention or physical activity advice.
Computer-tailored physical activity advice
EXPERIMENTALSubjects receive computer-tailored physical activity advice.
Interventions
Subjects receive advice regarding physical activities.
Eligibility Criteria
You may qualify if:
- Dutch speaking
- Age range: 18 - 65 years old
- Access to the Internet at work or at home
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Ghentlead
- Research Foundation Flanderscollaborator
Study Sites (1)
Ghent University - Department of Movement and Sports Sciences
Ghent, 9000, Belgium
Related Publications (1)
Compernolle S, Vandelanotte C, Cardon G, De Bourdeaudhuij I, De Cocker K. Effectiveness of a web-based, computer-tailored, pedometer-based physical activity intervention for adults: a cluster randomized controlled trial. J Med Internet Res. 2015 Feb 9;17(2):e38. doi: 10.2196/jmir.3402.
PMID: 25665498DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ilse De Bourdeaudhuij, PhD
University Ghent
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 4, 2014
First Posted
March 6, 2014
Study Start
May 1, 2012
Primary Completion
February 1, 2013
Study Completion
June 1, 2013
Last Updated
March 6, 2014
Record last verified: 2014-03