World Health Organization site
Skip Navigation Links

Main
Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 3 December 2012
Main ID:  NCT01473771
Date of registration: 14/11/2011
Primary sponsor: National Center for Telehealth and Technology
Public title: Caring Letters for Military Suicide Prevention
Scientific title: Caring Letters for Military Suicide Prevention: A Randomized Controlled Trial
Date of first enrolment: November 2011
Target sample size: 4730
Recruitment status: Enrolling by invitation
URL:  http://clinicaltrials.gov/show/NCT01473771
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention  
Countries of recruitment
Germany United States
Contacts
Name:   David D Luxton, PhD
Address: 
Telephone:
Email:
Affiliation:  National Center for Telehealth and Technology
Key inclusion & exclusion criteria

Inclusion Criteria:

- Current psychiatric inpatients

- Possess an active email account

- Informed consent

- Active duty military, Veteran, Retiree, National Guard or Reserves status

Exclusion Criteria:

- Not competent to consent

- Adverse behavioral problems

- The primary psychiatric nurse or attending psychiatrist considers that study to be
clinically inappropriate

- Currently under arrest/incarceration

- Involuntary committed for psychiatric care status



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Suicide
Suicide, Attempted
Intervention(s)
Behavioral: Caring Letter (email)
Primary Outcome(s)
Suicide Mortality Rates [Time Frame: Study Completion (2 years)]
Secondary Outcome(s)
Acquired Capability for Suicide Scale (ACSS) [Time Frame: Baseline]
Acquired Capability for Suicide Scale (ACSS) [Time Frame: Study Completion (2 years)]
Interpersonal Needs Questionnaire (INQ) [Time Frame: Baseline]
Interpersonal Needs Questionnaire (INQ) [Time Frame: Study Completion (2 years)]
Medically Admitted Self-Inflicted Injuries [Time Frame: Study Completion (2 years)]
Patient Health Questionnaire (PHQ-9) [Time Frame: Baseline]
Patient Health Questionnaire (PHQ-9) [Time Frame: Study Completion (2 years)]
Patient Satisfaction Survey [Time Frame: Baseline]
Patient Satisfaction Survey [Time Frame: Study Completion (2 Years)]
Suicide Ideation Scale (SIS) [Time Frame: Baseline]
Suicide Ideation Scale (SIS) [Time Frame: Study Completion (2 years)]
Time to Suicidal Behavior [Time Frame: Study Completion (2 years)]
Secondary ID(s)
MOMRP
W81XWH-11-2-0123
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Department of Defense
U.S. Army Medical Research and Materiel Command
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.1 - Version history