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ExerciseABCNCT03139643

Assessment of the Predictors and Moderators of Behavior Change

A study testing Cognitive Dissonance and Action Planning in people with Exercise, run by Boston University Charles River Campus.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Exercise
What is being tested?
Cognitive Dissonance and Action Planning
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
230 participants
Where
No sites listed yet
Study dates
Jun 2014to Jun 2017
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • None

About this study

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.

Conditions
Exercise
Being tested
Cognitive Dissonance, Action Planning, Reflection (Control Condition)
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cognitive DissonanceOther

    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 PlanningOther

    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)Other

    After reading the materials about their chosen behavior, participants will be asked to summarize and reflect on what they read.

Study groups in NCT03139643
Study groupRoleWhat they receive
Cognitive DissonanceExperimentalAfter 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.
Receives: Other: Cognitive Dissonance
Action PlanningExperimentalAfter 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.
Receives: Other: Action Planning
Reflection (Control Condition)Placebo comparatorAfter reading the materials about their chosen behavior, participants will be asked to summarize and reflect on what they read.
Receives: Other: Reflection (Control Condition)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: Change from baseline to 4 weeks

  2. 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.

    Measured: Change from baseline to 4 weeks

Secondary outcomes (9)
  1. Distress Intolerance Index

    Measure of distress intolerance.

    Measured: Change from baseline to 4 weeks

  2. UPPS Impulsive Behavior Scale (UPPS)

    Self-report measure of impulsivity.

    Measured: Change from baseline to 4 weeks

  3. Penn State Worry Questionnaire (PSWQ)

    Self-report measure of worry.

    Measured: Change from baseline to 4 weeks

  4. Self-Control Scale (SCS)

    Perceived self-control measure.

    Measured: Change from baseline to 4 weeks

  5. Delay Discounting Questionnaire

    Monetary choice task.

    Measured: Change from baseline to 4 weeks

  6. Pittsburgh Sleep Quality Index (PSQI)

    Self-report measure of sleep quality for the past month.

    Measured: Change from baseline to 4 weeks

  7. Center for Epidemiological Studies Depression Scale (CES-D)

    Self-report measure of depressive symptoms.

    Measured: Change from baseline to 4 weeks

  8. Beck Anxiety Inventory (BAI)

    Self-report measure of anxiety symptoms experienced in past week.

    Measured: Change from baseline to 4 weeks

  9. Generalized Self-Efficacy Scale

    Self-report measure of perceived self-efficacy.

    Measured: Change from baseline to 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 May 2017
  2. Study startJun 2014
  3. Primary completionDec 2016
  4. Study completionJun 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
230 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03139643
Sponsor's protocol ID
3555E
Acronym
ABC
Status last verified
May 2018
First submitted
29 Jul 2016
Last updated
20 Jul 2026
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Patten EA, Kredlow MA, Szuhany KL, Keshishian AC, Otto MW. Catching As and Zs: poor sleep quality predicts failures to increase studying time. Sleep Health. 2020 Feb;6(1):15-18. doi: 10.1016/j.sleh.2019.09.001. Epub 2019 Oct 31.

    PubMed 31676201

Questions about this trial

What is this clinical trial studying?

A study testing Cognitive Dissonance and Action Planning in people with Exercise, run by Boston University Charles River Campus.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

International Physical Activity Questionnaire (time frame: Change from baseline to 4 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03139643, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2026.

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