Clinical Trials Directory

Trials / Completed

CompletedNCT04881903

Developing a Mobile Intervention to Reduce Suicidal Cognitions in Veterans

Developing a Mobile Intervention to Reduce Suicidal Cognitions in Veterans (COR 19-490)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
VA Office of Research and Development · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Suicide cognitions are conceptualized as enduring, chronic vulnerability factors that predispose individuals to suicidal crises. Therefore, modification of these beliefs may reduce suicidal thoughts and behaviors. The goal of this research is to develop, refine, and pilot-test a mobile intervention to reduce cognitions that contribute to elevated suicide risk and to assess the impact of reductions in suicide cognitions and anger cognitions on suicide risk and functioning.

Detailed description

Suicide cognitions are conceptualized as enduring, chronic vulnerability factors that predispose individuals to suicidal crises. Therefore, modification of these beliefs may reduce suicidal thoughts and behaviors. In addition to suicide cognitions, another potentially modifiable risk factor for suicide is anger. The goal of this research is to develop, refine, and pilot-test a mobile interpretation bias modification intervention to reduce cognitions that contribute to elevated suicide risk and to assess the impact of reductions in suicide cognitions and hostile interpretation bias (a cognitive bias that is associated with anger) on suicide risk and functioning.

Conditions

Interventions

TypeNameDescription
BEHAVIORALMobile Intervention for Suicidal Thoughts (MIST)This is an interpretation bias modification intervention that is designed to target cognitive factors that contribute to suicide risk. Participants will be instructed to complete at least 5 treatment sessions per week for a period of 4 weeks. Each session takes approximately 10 minutes.
BEHAVIORALMobile Intervention for Reducing Anger (MIRA)This is an interpretation bias modification intervention that is designed to target hostile interpretation bias. Participants will be instructed to complete at least 5 treatment sessions per week for a period of 4 weeks. Each session takes approximately 10 minutes.

Timeline

Start date
2021-12-01
Primary completion
2024-02-01
Completion
2024-02-01
First posted
2021-05-11
Last updated
2025-02-20
Results posted
2025-02-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04881903. Inclusion in this directory is not an endorsement.