- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02562937
Reducing Sedentary Behaviour in University Students Using Text Messages
September 28, 2015 updated by: Dr. Harry Prapavessis, Western University, Canada
Reducing Sedentary Behaviour In University Students Using A Text Message-Based Intervention
The primary purpose of the current study was to determine whether a text message intervention would increase break frequency and length of break from sitting, time spent standing, and time spent in light and moderate intensity physical activity in university students
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Sedentary behaviour (SB) has been linked to many health problems (e.g., type 2 diabetes, heart disease).
Interventions aimed at office workers, overweight and obese individuals have proven successful in reducing SB; however, no studies have examined university students.Text message-based interventions have succeeded to aid in smoking cessation and increase both physical activity and healthy eating, but have not been shown to reduce SB.
Eighty-two university students were randomized into intervention (SB related text messages) or control (text messages unrelated to SB) groups.
Participants received daily text messages and reported various SBs (i.e., breaks from sitting, standing, light and moderate intensity physical activity) at four time points (baseline, 2, 4 and 6 weeks).
Study Type
Interventional
Enrollment (Actual)
82
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- be able to read and write English
- own a cell phone with unlimited incoming text messages
- be a student at Western University
Exclusion Criteria:
- be under 18 or over 64
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
text messages related to sedentary behaviour
|
texts sent twice daily encouraging reduced sedentary behaviour
|
|
No Intervention: Control
text messages unrelated to sedentary behaviour.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in length of break from sitting in minutes
Time Frame: baseline, 2, 4, and 6 weeks
|
baseline, 2, 4, and 6 weeks
|
|
Change in frequency of break from sitting in minutes
Time Frame: baseline, 2, 4, and 6 weeks
|
baseline, 2, 4, and 6 weeks
|
|
Change in minutes spent standing
Time Frame: baseline, 2, 4, and 6 weeks
|
baseline, 2, 4, and 6 weeks
|
|
Change in minutes spent in light intensity physical activity
Time Frame: baseline, 2, 4, and 6 weeks
|
baseline, 2, 4, and 6 weeks
|
|
Change in minutes spent in moderate intensity physical activity
Time Frame: baseline, 2, 4, and 6 weeks
|
baseline, 2, 4, and 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in self-efficacy for sedentary behaviour measured by percentage of confidence
Time Frame: baseline, 2, 4, and 6 weeks
|
purpose-built self-efficacy questionnaire used to rate how confident one feels in reducing sedentary behaviour
|
baseline, 2, 4, and 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2015
Primary Completion (Actual)
March 1, 2015
Study Completion (Actual)
March 1, 2015
Study Registration Dates
First Submitted
September 25, 2015
First Submitted That Met QC Criteria
September 28, 2015
First Posted (Estimate)
September 29, 2015
Study Record Updates
Last Update Posted (Estimate)
September 29, 2015
Last Update Submitted That Met QC Criteria
September 28, 2015
Last Verified
September 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- ECotten
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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