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Clinical Trials/NCT04129866
NCT04129866
Unknown
Not Applicable

Mobile Interpretation Bias Modification Clinical Trial

University of Southern Mississippi1 site in 1 country114 target enrollmentDecember 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety Sensitivity
Sponsor
University of Southern Mississippi
Enrollment
114
Locations
1
Primary Endpoint
Anxiety Sensitivity Index-3 Cognitive Concerns Subscale
Last Updated
3 years ago

Overview

Brief Summary

The Mobile-Interpretation Bias Modification clinical trial aims to examine the efficacy of a brief mobile phone delivered interpretation bias modification to reduce anxiety sensitivity cognitive concerns and suicidal ideation in National Guard Personnel. The investigators propose a randomized controlled trial testing the efficacy, acceptability, and usability of M-IBM with a sample of 114 National Guardsmen with current suicidal ideation and elevated anxiety sensitivity cognitive concerns. Participants will complete assessments, receive assistance on installing M- IBM on their phone, complete an M-IBM intervention session, and complete post-intervention assessments. Baseline measures of psychopathology, and usability/acceptability of M-IBM will be obtained during the initial session. In addition, 1-month, and 3-month follow-ups would be scheduled to examine changes in psychopathology. The investigators hypothesize that those randomized to M-IBM will experience reductions in anxiety sensitivity cognitive concerns, suicidal ideation. In addition participants will find M-IBM acceptable and easy to use.

Registry
clinicaltrials.gov
Start Date
December 15, 2019
End Date
March 29, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Elevated ASCC (\>2) and include only Guard members who also have current SI (\> 0) .
  • Ownership of a smartphone

Exclusion Criteria

  • those determined by military or study personnel to be actively psychotic, manic, or imminently suicidal and in need of emergency services

Outcomes

Primary Outcomes

Anxiety Sensitivity Index-3 Cognitive Concerns Subscale

Time Frame: 3 months post intervention

Range 0 - 24, Higher Scores mean more pathology

The Self-Injurious Thoughts and Behaviors Interview

Time Frame: 3 months post intervention

Study Sites (1)

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