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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date May 2018
Source Boston University Charles River Campus
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cognitive Dissonance
After reading the materials about their chosen behavior, participants will be asked write an essay about their behavior of choice (studying/exercising). For this essay they will be asked to imagine that they have reached their ideal level of academic achievement/fitness, describe what this would look and feel like, and reflect on how this would impact how they view themselves, their relationships, and their day to day life.
Action Planning
After reading the materials about their chosen behavior, participants will be asked to make a detailed plan for the following two weeks based on the following items taken from a study by Sniehotta and colleagues (2004): 1) when to complete studying/exercise, 2) where to complete studying/exercise, 3) how to complete studying/exercise (e.g., what types of exercise- cardio, class, etc. or what types of studying activities- reading, taking notes, creating outlines, etc.), and 4) how often to complete studying/exercise. Participants will be given a calendar as an aid to planning their behavior.
Reflection (Control Condition)
After reading the materials about their chosen behavior, participants will be asked to summarize and reflect on what they read.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Boston University Charles River Campus

Outcome

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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