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Clinical Trials/NCT04129866
NCT04129866UnknownNot Applicable

Mobile Interpretation Bias Modification Clinical Trial

University of Southern Mississippi2 sites in 1 country114 target enrollmentStarted: December 15, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
114
Locations
2
Primary Endpoint
Anxiety Sensitivity Index-3 Cognitive Concerns Subscale

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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