NCT06547008

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
57

participants targeted

Target at P50-P75 for phase_1

Timeline
26mo left

Started Mar 2025

Typical duration for phase_1

Geographic Reach
1 country

3 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress37%
Mar 2025Aug 2028

First Submitted

Initial submission to the registry

July 11, 2024

Completed
29 days until next milestone

First Posted

Study publicly available on registry

August 9, 2024

Completed
7 months until next milestone

Study Start

First participant enrolled

March 19, 2025

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2028

Last Updated

October 20, 2025

Status Verified

October 1, 2025

Enrollment Period

2.5 years

First QC Date

July 11, 2024

Last Update Submit

October 14, 2025

Conditions

Keywords

suicidemilitary

Outcome Measures

Primary Outcomes (3)

  • Reach - Self

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

    Year 1

  • Reach - Intervening for others

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

    Year 1

  • Reach - Interactions with soldiers involving discussions about suicide risk

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

    Weekly for 1 year

Secondary Outcomes (8)

  • Suicidal ideation

    Year 1

  • Suicide plans:

    Year 1

  • Suicide attempts

    Year 1

  • Adoption

    Up to 24 months

  • Implementation

    Up to 24 months

  • +3 more secondary outcomes

Other Outcomes (3)

  • Intentions, attitudes, norms

    Baseline, quarterly, year 1, year 2

  • Organizational culture

    Baseline, quarterly, year 1, year 2

  • Maintenance

    Up to 24 months

Study Arms (2)

Army-SPRING

EXPERIMENTAL

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

Behavioral: Army-SPRING

Risk Reduction Group (Control)

PLACEBO COMPARATOR

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

Behavioral: Risk Reduction Group (Control)

Interventions

Army-SPRINGBEHAVIORAL

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

Army-SPRING

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

Risk Reduction Group (Control)

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Connecticut Army National Guard

Hartford, Connecticut, 06103, United States

NOT YET RECRUITING

Yale University

New Haven, Connecticut, 06520, United States

ACTIVE NOT RECRUITING

Center for the Treatment and Study of Anxiety, University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

RECRUITING

MeSH Terms

Conditions

Suicide

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Lily Brown, PhD

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR
  • Ashley Hagaman, PhD

    Yale University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 11, 2024

First Posted

August 9, 2024

Study Start

March 19, 2025

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

August 1, 2028

Last Updated

October 20, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will share

We will upload data into the NIMH Data Archives every 6 months.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Time Frame
Each 6 months once official data collection begins.
Access Criteria
Determined by the NIMH
More information

Locations