NCT07072819

Brief Summary

This pilot study evaluates the acceptability, appropriateness, and feasibility of a new crisis response training called Crisis Ready.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
27

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 12, 2025

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

June 25, 2025

Completed
23 days until next milestone

First Posted

Study publicly available on registry

July 18, 2025

Completed
13 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
8 months until next milestone

Results Posted

Study results publicly available

March 13, 2026

Completed
Last Updated

March 13, 2026

Status Verified

February 1, 2026

Enrollment Period

2 months

First QC Date

June 25, 2025

Results QC Date

November 3, 2025

Last Update Submit

February 20, 2026

Conditions

Keywords

suicideoverdose988naloxone

Outcome Measures

Primary Outcomes (2)

  • Acceptability of Intervention Measure

    Participants' perspectives of the likability of the intervention. Scores range from 4 to 20, with higher scores indicating higher levels of acceptability.

    Post-intervention (approximately 90 minutes on one day)

  • Intervention Appropriateness Measure

    Measures the fit of the intervention for the population. Scores range from 4 to 20 with higher scores indicating higher levels of appropriateness.

    Post-intervention (approximately 90 minutes on one day)

Secondary Outcomes (5)

  • Perceptions of the Crisis Ready Training

    Post-intervention (approximately 90 minutes on one day)

  • Attitudes About 988

    Post-intervention (approximately 90 minutes on one day)

  • Perception of 988

    Post-intervention (approximately 90 minutes on one day)

  • Knowledge of Naloxone

    Post-intervention (approximately 90 minutes on one day)

  • Attitudes About Naloxone

    Pre- and Post-intervention (approximately 90 minutes on one day)

Study Arms (1)

Crisis Ready Training

EXPERIMENTAL

This is an open label pilot of a new psychoeducational Intervention called the Crisis Ready Training. The intervention combines Crisis Line Facilitation and Take Home Naloxone trainings.

Behavioral: Crisis Ready Training

Interventions

Crisis Ready Training combines Crisis Line Facilitation with Take Home Naloxone training. The intervention is delivered in a group format.

Crisis Ready Training

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Participates in the Baltimore Crisis Response, Inc Law Enforcement Assisted Diversion Program
  • Capacity to give informed consent

You may not qualify if:

  • Unable to understand English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Baltimore Crisis Response, Inc.

Baltimore, Maryland, 21201, United States

Location

MeSH Terms

Conditions

SuicideDrug Overdose

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehaviorPrescription Drug MisuseDrug MisuseSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Limitations and Caveats

This pilot study enrolled only 27 participants from one law enforcement assisted diversion program. Additionally, outcomes were observed only immediately after the intervention. Results should be interpreted in light of the small sample size, sampling bias, and lack of follow-up time points.

Results Point of Contact

Title
Dr. Alison Athey
Organization
RAND

Study Officials

  • Alison J Athey, PhD

    RAND

    PRINCIPAL INVESTIGATOR
  • Sapna Mendon-Plasek, PhD

    RAND

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Behavioral Scientist

Study Record Dates

First Submitted

June 25, 2025

First Posted

July 18, 2025

Study Start

June 12, 2025

Primary Completion

July 31, 2025

Study Completion

July 31, 2025

Last Updated

March 13, 2026

Results First Posted

March 13, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will share

De-identified quantitative data will be stored and shared by the National Center for Health and Justice Integration for Suicide Prevention at Michigan State University.

Time Frame
Data will be shared upon completion of all study activities and maintained for a duration that complies with the policy of the National Institute on Mental Health.
Access Criteria
Data may be accessed by researchers who submit a data request proposal and are approved by the Center.
More information

Locations