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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04129866
Other study ID # W81XWH-16-2-0004
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date December 15, 2019
Est. completion date March 29, 2023

Study information

Verified date May 2022
Source University of Southern Mississippi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 114
Est. completion date March 29, 2023
Est. primary completion date March 29, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
M-IBM
In this paradigm, an ambiguous word or two-word phrase related to ASCC is followed by a sentence that resolves the word-sentence meaning as threatening or benign. For example, participants are presented with an ambiguous word or two-word phrase for 1 second. On half the trials the combination of the word/phrase and sentence creates a benign meaning (as in the previous example). On the other half of trials this combination creates an anxious-threat meaning Participants are required to judge the relatedness of the word/phrase and the sentence. Participants are given feedback during training such that judging the anxious-threat combinations to be "unrelated" and the benign combinations as being "related" would produce a "correct" response. In contrast, if participants produce an "incorrect" response they see "incorrect".
Control-IBM
Placebo IBM where sentences are not related to anxious threat meaning of cue word.

Locations

Country Name City State
United States University of Southern Mississippi Hattiesburg Mississippi

Sponsors (2)

Lead Sponsor Collaborator
University of Southern Mississippi Military Suicide Research Consortium

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety Sensitivity Index-3 Cognitive Concerns Subscale Range 0 - 24, Higher Scores mean more pathology 30 minutes
Primary Anxiety Sensitivity Index-3 Cognitive Concerns Subscale Range 0 - 24, Higher Scores mean more pathology 1 month post intervention
Primary Anxiety Sensitivity Index-3 Cognitive Concerns Subscale Range 0 - 24, Higher Scores mean more pathology 3 months post intervention
Primary The Self-Injurious Thoughts and Behaviors Interview 1 month post intervention
Primary The Self-Injurious Thoughts and Behaviors Interview 3 months post intervention
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