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NCT Number: NCT06547008

Army-SPRING Army-Suicide Prevention Research

Every unit in the Connecticut Army National Guard has a Suicide Intervention Officer to provide suicide intervention education awareness for their unit, monitor for soldiers in crisis and connect soldiers with helping resources and agencies. Suicide Intervention Officers need support in this difficult role, yet there is limited guidance on how to help them. This study will shed light on how to support Suicide Intervention Officers and whether this support results in reduced suicide risk in their units.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Connecticut Army National Guard, Hartford, Connecticut, United States

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About this study

Attachment 4: Lay Abstract Objective 1: The first objective is to spend 6 months collecting feedback from Army National Guard Soldiers and their family, the religious affairs team, and leadership on how best to reduce risk for suicide. We will also collect feedback from Suicide Intervention Officers, who are appointed to reduce risk for suicide in their unit, about how to support these officers in their important work.

Objective 2: The second objective is to compare two strategies to support Suicide Intervention Officers as they work closely with soldiers to reduce their risk for suicide. The 47 Suicide Intervention Officers in the Connecticut Army National Guard will be randomly assigned (like the flip of a coin) to one of two groups. The first group will attend an extra training (Control Group). The second group will become part of a community focused on reducing suicide risk, including access to online forums to support them in their work, support in leading Battle Drills focused on suicide prevention, and additional training and consultation (Army-SPRING Group). Chaplains/religious affairs specialists will also receive the Army-SPRING group training, but will not be randomized since there are only 5 total Chaplains and 5 religious affairs specialists.

Objective 3: The third objective is to study whether soldiers with Suicide Intervention Officers in the Army-SPRING Group (described in objective 2) report lower rates of suicide ideation and attempts than the Control Group.

Rationale: Every unit in the Connecticut Army National Guard has a Suicide Intervention Officer to provide suicide intervention education awareness for their unit, monitor for soldiers in crisis and connect soldiers with helping resources and agencies. Suicide Intervention Officers need support in this difficult role, yet there is limited guidance on how to help them. This study will shed light on how to support Suicide Intervention Officers and whether this support results in reduced suicide risk in their units.

CBPR Approach and Implementation: We have formed a community advisory board that includes Veterans of Army National Guard units in other states (Pennsylvania); Veterans of the Army with employment as a civilian in the Marines, Chaplains in the Connecticut National Guard on the Air Force (who are intimately familiar with the needs at CT but who are not employees of the Army National Guard), and members of the Suicide Prevention Task force. We have asked for their feedback on the design of the study and will meet with them monthly for the three months and then quarterly thereafter.

FY23 TBIPHRP HSRA Focus Area: This project relates to the Prevent and Assess area of encouragement namely: "Development, evaluation, and implementation of crosscutting prevention approaches targeting upstream factors or leveraging communities and peers to address multiple adverse outcomes such as suicide." Types of Patients Helped by the Research and How it will Help Them: This research will help Army National Guard Soldiers, who are at higher risk for suicide than Active Duty service members. It will help them by supporting Suicide Intervention Officers as they work to reduce risk for suicide among soldiers.

Potential clinical applications, Benefits and Risks: The clinical application is a strategy to support Suicide Intervention Officers, which could benefit soldiers in reducing their suicide risk.

Projected timeline: 4 years, including 6 months of preparatory work with our community advisory board, who will also provide input throughout.

Health and well-being of Service Members: This will help the health and well-being of service members by reducing their risk for suicide. It will help Suicide Intervention Officers by improving their confidence in supporting soldiers who are struggling with suicide risk. It will help Chaplains/Religious affairs specialists who regularly desire more training in suicide prevention and who are a well-used source of support for soldiers at risk.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Serving as an SIO or chaplain/religious affairs specialist for a unit of the CTARNG
  • Willing to provide informed consent.

Exclusion criteria

  • None

Treatment and study plan

Army-SPRING

Behavioral

Army-SPRING includes a package of implementation options to support implementation of suicide prevention duties

Risk Reduction Group (Control)

Behavioral

Risk Reduction Group is a mandated training from National Guard Service members

Primary outcomes

  1. Reach - Self

    Time frame: Year 1

    Use of suicide prevention services for self, URI-3 item 75

  2. Reach - Intervening for others

    Time frame: Year 1

    Use of suicide prevention services for buddy, URI-3 item 74

  3. Reach - Interactions with soldiers involving discussions about suicide risk

    Time frame: Weekly for 1 year

    Number of soldier interactions reporting suicide risk/Total number of interactions with soldiers

Secondary outcomes

  1. Suicidal ideation

    Time frame: Year 1

    URI-3 item 15

  2. Suicide plans:

    Time frame: Year 1

    URI-3 item 15a

  3. Suicide attempts

    Time frame: Year 1

    URI-3 item 15b

  4. Adoption

    Time frame: Up to 24 months

    Suicide intervention officer willingness to initiate all SIO duties; This will be operationalized as the total number of SIOs who reported willingness to complete all their suicide prevention-related activities

  5. Implementation

    Time frame: Up to 24 months

    Fidelity to all assigned suicide intervention officer duties; Fidelity will be assessed using self-report by the SIO, including the following questions: 1) Does your battalion know that you are their SIO?; and 2) Have you completed any trainings related to suicide prevention with your battalion? Finally, among SIOs randomized to ARMY-SPRING, we will assess their fidelity of leading the battle drills in a manner consistent with suicide prevention principals.

  6. Acceptability

    Time frame: Up to 24 months

    Acceptability of Intervention Measure (AIM)

  7. Appropriateness

    Time frame: Up to 24 months

    Intervention appropriateness measure (IAM)

  8. Qualitative Interviews

    Time frame: Up to 24 months

    Qualitative Interviews (Acceptability, appropriateness, climate, etc.)

Other outcomes

  1. Intentions, attitudes, norms

    Time frame: Baseline, quarterly, year 1, year 2

    Theory of Planned Behavior Questionnaire

  2. Organizational culture

    Time frame: Baseline, quarterly, year 1, year 2

    We use the support subscale of the Implementation Leadership Scale to assess how leadership influences implementation outcomes. Organizational culture measures the culture and climate in their battalion, feasibility and acceptability of implementing suicide prevention tasks

  3. Maintenance

    Time frame: Up to 24 months

    Suicidal ideation: URI-3 item 15; Suicide plans: URI-3 item 15a

Study contacts

Contact information is provided by the study sponsor or research team.

Lily A Brown, PhD

CONTACT

[email protected]

215-746-3346

Marin Kautz, PhD

CONTACT

[email protected]

805-235-7100

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Collaborators

  • Yale University

Registry information

Official study title

Army-Suicide Prevention Research on Implementation in the National Guard (Army-SPRING)

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Aug 9, 2024
Registry last updated
Oct 20, 2025

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.

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