Naval Medical Center San Diego
San Diego, California, 92134, United States
NCT Number: NCT05795764
The study is a randomized trial comparing outcomes of active duty service members who present to the emergency department at risk for suicide and receive care from providers trained in crisis response planning versus those providing treatment as usual.
This study is active but is not currently recruiting participants.
18 year and older
All sexes
Interventional
Not applicable
San Diego, California, 92134, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Crisis Response Planning (CRP) is a brief psychotherapeutic intervention.
Other names: CRP
Standard care provided for patients at risk for suicide
Time frame: Through study completion, an average of 1 year
Assessment of suicide attempts
Time frame: Through study completion, an average of 1 year
Assessment of suicidal ideation; 19 items rated on a scale 0-2, higher scores indicate greater suicidal ideation severity
United States Naval Medical Center, San Diego
Fed
Moderators of the Effectiveness of Crisis Response Planning (CRP) for Military Personnel
Acronym: ASPIS/CRP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06614946
Behavior, Behavioral Symptoms
Ann Arbor, Michigan, United States
View Trial DetailsNCT07661901
Anhedonia, Behavior
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT05021224
Behavior, Behavioral Symptoms
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT04896151
Behavior, Behavioral Symptoms
Columbus, Ohio, United States
View Trial Details