Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
74 participants
INTERVENTIONAL
2013-10-31
2016-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cognitive Anxiety Sensitivity Treatment for Suicide
NCT01947179
Mindfulness-Based Cognitive Therapy for Suicide Prevention
NCT01872338
Implementation of an Evidence Based Post-Traumatic Stress Disorder (PTSD) Treatment in Public Sector Settings
NCT01488539
Computerized Cognitive Bias Intervention for Intolerance of Uncertainty
NCT02818296
Investigation of the Freespira Breathing System in the Treatment of Post Traumatic Stress Disorder (PTSD)
NCT03039231
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
The anxiety risk reduction condition will be a combination of psychoeducation plus Cognitive Bias Modification (CBM-I) for anxiety sensitivity (AS). The psychoeducational component will focus on the nature of stress and its effect on the body. Interoceptive exposure (IE) exercises, designed to correct the conditioned fear to these bodily sensations, will be explained and practiced.
Cognitive Anxiety Sensitivity Treatment
Control
The control condition will be a combination of information about general health and wellness (e.g. diet, exercise etc.) plus an inert Cognitive Bias Modification (CBM-I) task.
Physical Health Education Training
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Cognitive Anxiety Sensitivity Treatment
Physical Health Education Training
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Show evidence of current suicidal ideation (BSS above 6.
* Show elevated AS indicated by scoring at or above the community sample mean on the ASI-Cog (above 9.
Exclusion Criteria
* Current or past psychotic-spectrum disorders or uncontrolled bipolar disorder
* No current substance dependence
* Must be an English speaker.
* Must be 18 years or older.
* Must have normal or corrected vision
* Cannot begin treatment/therapy within 1 month of baseline.
* Cannot begin a new medication within 3 months of baseline.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Florida State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Norman Schmidt
Distinguished Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Anxiety and Behavioral Health Clinic
Tallahassee, Florida, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Schmidt NB, Norr AM, Allan NP, Raines AM, Capron DW. A randomized clinical trial targeting anxiety sensitivity for patients with suicidal ideation. J Consult Clin Psychol. 2017 Jun;85(6):596-610. doi: 10.1037/ccp0000195. Epub 2017 Mar 13.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RF02397
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.