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Wingman-Connect for Suicide Prevention
N/A
Waitlist Available
Research Sponsored by University of Rochester
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 years
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the Wingman-Connect training program, which helps new Airmen build strong social connections and healthy coping habits to prevent suicide. The program targets first-term Airmen who may be more vulnerable to stress. It works by creating a supportive community and teaching effective stress management.
Who is the study for?
This trial is for US Air Force bases, specifically those in the Air Force Global Strike Command and Air Mobility Command. It involves around 96 implementers responsible for delivering Wingman-Connect training to first-term Airmen, with an estimated total of 17,400 Airmen participating across all bases.
What is being tested?
The study tests the impact of Wingman-Connect, a suicide prevention program implemented at eight operational AF bases. The effectiveness will be measured by analyzing base-level suicide attempt rates before and after the intervention over a period of 51 months using a randomized stepped-wedge design.
What are the potential side effects?
Since this trial focuses on implementing a training program rather than a medical intervention, traditional side effects are not applicable. However, there may be psychological impacts or changes in behavior among participants that could arise from their involvement in the program.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Total Number Base level suicide attempts among Ranks E1-4
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Wingman-ConnectExperimental Treatment1 Intervention
Wingman-Connect (Wyman et al., 2020) uses a network health theoretical framework to strengthen two suicide-protective functions of social networks: 1) Strengthening positive social bonds, and 2) Building healthy norms that incentivize adaptive coping. Training will be delivered in First Term Airmen classes among all Airmen arriving at base during the study period.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for suicide prevention, such as the Wingman-Connect program, focus on fostering social connectedness and building resilience. These interventions work by creating strong support networks and enhancing individuals' ability to cope with stress and emotional challenges.
This approach is crucial for suicide prevention patients as it directly addresses feelings of isolation and provides a sense of belonging and support, which are essential for mitigating suicidal thoughts and behaviors.
Reports on the Perceived Advantages and Disadvantages of Suicidal Behavior by Patients With Depression.
Reports on the Perceived Advantages and Disadvantages of Suicidal Behavior by Patients With Depression.
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Who is running the clinical trial?
University of RochesterLead Sponsor
867 Previous Clinical Trials
531,482 Total Patients Enrolled
4 Trials studying Suicide Prevention
70,705 Patients Enrolled for Suicide Prevention
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Eligibility Criteria:
This trial includes the following eligibility criteria:- Not applicable.
Research Study Groups:
This trial has the following groups:- Group 1: Wingman-Connect
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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