- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01482234
Text Messages and Physical Activity Among Teens
January 18, 2016 updated by: Deborah Thompson, Baylor College of Medicine
TXT Me: Texting Motivational Messages Encouraging Adolescent Physical Activity
The purpose of this study is to assess whether text messages can be used as a way to increase the amount of physical activity teens get each day.
Study Overview
Detailed Description
This research will develop an innovative intervention that promotes physical activity to 14-17 year olds (roughly high school aged youth).
It is guided by Self Determination Theory and seeks to enhance adolescents' feelings of physical activity autonomy, competence, and relatedness, key psychological needs related to motivation to be physically active.
The physical activity to be promoted is walking, which has broad appeal and can be performed as part of usual-day activities.
Since youth are heavy users of cell phones and texting, the intervention will send theoretically-grounded text messages designed to enhance physical activity.
Study Type
Interventional
Enrollment (Actual)
160
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Texas
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Houston, Texas, United States, 77030
- Baylor College of Medicine
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-
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
14 years to 17 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 14-17 years old
- access to a computer with high speed internet access
- home email address
- cell phone that can send/receive text messages
- text message plan
- fluent in English
Exclusion Criteria:
- mental or physical limitations that impair ability to fully participate in the program and/or complete baseline and post assessment data collection.
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: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: pedometers only
Participants randomized to this arm will receive pedometers only.
They will participate in baseline and 3 months data collection.
|
text messages, physical activity, self determination theory, extrinsic motivation, intrinsic motivation, pedometers, walking, prompts
|
|
Experimental: pedometers + prompts
Participants randomized to this arm will receive pedometers plus a weekly prompt to set a step goal.
They will participate in baseline and 3 months data collection.
|
text messages, physical activity, self determination theory, extrinsic motivation, intrinsic motivation, pedometers, walking, prompts
|
|
Experimental: pedometer + prompt + messages
Participants randomized to this arm will receive pedometers, weekly prompts, and 6 motivational text messages a week.
They will participate in baseline and 3 months data collection.
|
text messages, physical activity, self determination theory, extrinsic motivation, intrinsic motivation, pedometers, walking, prompts
|
|
No Intervention: Control
Participants randomized to this group will participate in data collection only; they will not receive an intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
physical activity
Time Frame: 3 months
|
physical activity will be assessed for 7 days at each data collection period; accelerometers will be used to assess physical activity amount and intensity
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3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological need satisfaction in exercise
Time Frame: 3 months
|
This scale will be used to assess psychological needs related to exercise - autonomy, relatedness, and competence
|
3 months
|
|
Behavioral Regulation in Exercise
Time Frame: 3 months
|
This scale will be used to assess motivation for exercise
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3 months
|
|
Satisfaction
Time Frame: 3 months
|
Satisfaction with the study will be assessed using standard questions
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3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Deborah Thompson, PhD, Baylor College of Medicine
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.
General Publications
- Thompson D, Cantu D, Ramirez B, Cullen KW, Baranowski T, Mendoza J, Anderson B, Jago R, Rodgers W, Liu Y. Texting to Increase Adolescent Physical Activity: Feasibility Assessment. Am J Health Behav. 2016 Jul;40(4):472-83. doi: 10.5993/AJHB.40.4.9.
- Thompson D, Cantu D, Bhatt R, Baranowski T, Rodgers W, Jago R, Anderson B, Liu Y, Mendoza JA, Tapia R, Buday R. Texting to Increase Physical Activity Among Teenagers (TXT Me!): Rationale, Design, and Methods Proposal. JMIR Res Protoc. 2014 Mar 12;3(1):e14. doi: 10.2196/resprot.3074.
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
February 1, 2012
Primary Completion (Actual)
August 1, 2013
Study Completion (Actual)
December 1, 2013
Study Registration Dates
First Submitted
November 28, 2011
First Submitted That Met QC Criteria
November 29, 2011
First Posted (Estimate)
November 30, 2011
Study Record Updates
Last Update Posted (Estimate)
January 20, 2016
Last Update Submitted That Met QC Criteria
January 18, 2016
Last Verified
January 1, 2016
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- H-27537
- R21HD066305 (U.S. NIH Grant/Contract)
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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