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Clinical Trials/NCT03280472
NCT03280472UnknownNot Applicable

Transition to College/Miami University

Miami University2 sites in 1 country60 target enrollmentStarted: September 18, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
60
Locations
2
Primary Endpoint
Change in Student Adjustment to College Questionnaire

Study Overview

Brief Summary

The current project will test whether a computerized training program, Cognitive Bias Modification (CBM), can be used as a prevention inoculation tool to reduce vulnerability to anxiety among incoming college students. Those not in the CBM condition will complete a symptom tracking condition (ST). We will also test whether ST influences vulnerability to anxiety among incoming college students.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • First and Second year students
  • Entered college in fall of 2017
  • Fluent in English
  • LSAS-SR score greater than or equal to 14 and less than or equal to 74.

Exclusion Criteria

  • Not provided

Arms & Interventions

Cognitive Bias Modification

Experimental

Participants will complete three session of cognitive bias modification.

Intervention: Cognitive Bias Modification (Behavioral)

Symptom Tracking

Other

Participants will track their symptoms.

Intervention: Symptom tracking (Behavioral)

Outcomes

Primary Outcomes

Change in Student Adjustment to College Questionnaire

Time Frame: Participants report on their past few days. The SACQ is administered at T1-T5. T2 occurs within ~1 week of T1/baseline. T2-T5 are spaced ~1 week apart from each other. Sessions are ~60-90 minutes.

Self-report on the degree to which the participant feels they are transitioning to college successfully.

Secondary Outcomes

  • Change in Interpretations(Participants report interpretations to a variety of situations. The IQ is administered at T1 and T4. T2 occurs within 1 week of T1/baseline. T2-T5 are spaced ~1 week apart from each other. Sessions are ~60-90 minutes.)
  • Change in Liebowitz Social Anxiety Scale-Self-Report(Participants report on symptoms during the past week. The LSAS-SR is administered at T1-T5. T2 occurs within ~1 week of T1/baseline. T2-T5 are spaced ~1 week apart from each other. Sessions are ~60-90 minutes.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Elise Clerkin

Assistant Professor

Miami University

Study Sites (2)

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