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Transition to College/Miami University

M

Miami University

Status

Unknown

Conditions

Interpretation Bias Modification
Symptom Tracking

Treatments

Behavioral: Symptom tracking
Behavioral: Cognitive Bias Modification

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Cognitive Bias Modification
Experimental group
Description:
Participants will complete three session of cognitive bias modification.
Treatment:
Behavioral: Cognitive Bias Modification
Symptom Tracking
Other group
Description:
Participants will track their symptoms.
Treatment:
Behavioral: Symptom tracking

Trial contacts and locations

1

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Central trial contact

Elise M Clerkin, PhD

Data sourced from clinicaltrials.gov

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