Exercise Clinical Trial
— ABCOfficial title:
Assessment of the Predictors and Moderators of Behavior Change
NCT number | NCT03139643 |
Other study ID # | 3555E |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2014 |
Est. completion date | June 2017 |
Verified date | May 2018 |
Source | Boston University Charles River Campus |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The current study aims to investigate two potential interventions (i.e., cognitive dissonance and action planning) for inducing behavior change for behaviors important to college students—studying and exercise. In addition, this study will investigate factors that may impact behavior change, such as psychological and neuropsychological variables, to better understand how to bridge the intention-behavior gap.
Status | Completed |
Enrollment | 230 |
Est. completion date | June 2017 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Boston University Psychology 101 students at least 18 years of age - Able to provide informed consent for the study - Sufficient command of the English language - Have experience using a computer and mouse Exclusion Criteria: |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Boston University Charles River Campus |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | International Physical Activity Questionnaire | Participants who choose to change their exercising behavior will be administer only this outcome measure; therefore, all participants only complete 1 primary outcome measure. | Change from baseline to 4 weeks | |
Primary | Studying Questionnaire | Participants who choose to change their studying behavior will be administered only this outcome measure; therefore, all participants only complete 1 primary outcome measure. | Change from baseline to 4 weeks | |
Secondary | Distress Intolerance Index | Measure of distress intolerance. | Change from baseline to 4 weeks | |
Secondary | UPPS Impulsive Behavior Scale (UPPS) | Self-report measure of impulsivity. | Change from baseline to 4 weeks | |
Secondary | Penn State Worry Questionnaire (PSWQ) | Self-report measure of worry. | Change from baseline to 4 weeks | |
Secondary | Self-Control Scale (SCS) | Perceived self-control measure. | Change from baseline to 4 weeks | |
Secondary | Delay Discounting Questionnaire | Monetary choice task. | Change from baseline to 4 weeks | |
Secondary | Pittsburgh Sleep Quality Index (PSQI) | Self-report measure of sleep quality for the past month. | Change from baseline to 4 weeks | |
Secondary | Center for Epidemiological Studies Depression Scale (CES-D) | Self-report measure of depressive symptoms. | Change from baseline to 4 weeks | |
Secondary | Beck Anxiety Inventory (BAI) | Self-report measure of anxiety symptoms experienced in past week. | Change from baseline to 4 weeks | |
Secondary | Generalized Self-Efficacy Scale | Self-report measure of perceived self-efficacy. | Change from baseline to 4 weeks |
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