- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03363737
Transtheoretical Model of Behavior Change and Anxiety
December 5, 2017 updated by: Paul D. Loprinzi, University of Mississippi, Oxford
Can Facebook Reduce Perceived Anxiety Among College Students? A Randomized Controlled Exercise Trial Using the Transtheoretical Model of Behavior Change
Examine the utility of the Transtheoretical Model in influencing anxiety among college students.
Employ a randomized controlled intervention including a static and dynamic Facebook intervention.
The static group accessed a Facebook page featuring 96 statuses.
Statuses were intended to engage cognitive processes, followed by behavioral processes of change per the Transtheoretical Model of behavior change.
Content posted on the static Facebook page was identical to the dynamic page.
However, the static group viewed all 96 statuses on the first day of the study, while the dynamic group received only 1-2 of these status updates per day throughout the intervention.
Anxiety was measured using the Overall Anxiety Severity and Impairment Scale (OASIS).
Time spent engaging in physical activity was assessed using the International Physical Activity Questionnaire (IPAQ).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
39
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 35 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Having an active Facebook account
- Daily access to a Smart Phone
- Current University of Mississippi email account
Exclusion Criteria:
- Outside the age range of 18-35
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: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Static
|
Exposure to content on Facebook, either daily (dynamic) or just at one time period (static).
|
|
EXPERIMENTAL: Dynamic
|
Exposure to content on Facebook, either daily (dynamic) or just at one time period (static).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Anxiety
Time Frame: At baseline and at the end of the 8-week intervention
|
OASIS, Overall Anxiety Severity and Impairment Scale.
There are 5 questions in this scale, with each question including 5 response options (ranging from 0-4).
The total score is reported, which ranges from 0-20 (higher score indicates greater anxiety).
|
At baseline and at the end of the 8-week intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (ACTUAL)
October 18, 2016
Primary Completion (ACTUAL)
August 24, 2017
Study Completion (ACTUAL)
August 24, 2017
Study Registration Dates
First Submitted
November 29, 2017
First Submitted That Met QC Criteria
December 4, 2017
First Posted (ACTUAL)
December 6, 2017
Study Record Updates
Last Update Posted (ACTUAL)
December 7, 2017
Last Update Submitted That Met QC Criteria
December 5, 2017
Last Verified
December 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 17-018
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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