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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03755206
Other study ID # IRB00008138
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 10, 2018
Est. completion date April 24, 2024

Study information

Verified date May 2024
Source Johns Hopkins Bloomberg School of Public Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The proposed study is part of the research project for a National Institute of Mental Health K01 grant to Dr. Haroz. The overall research project is focused on understanding how to sustain evidenced-based mental and behavioral health programs in tribal contexts. The aim of this study is to pilot test sustainment strategy interventions across tribal settings using mixed-methods.


Description:

Among the most pressing issues in mental health Dissemination and Implementation research (D&I) is the lack of knowledge about how to sustain mental health prevention and treatment services for which there is substantial evidence of impact. Most D&I studies focus on adoption and initial implementation, with few studies (<20) rigorously exploring sustainment. The sustainment of services has been described as "one of the greatest, yet least understood, challenges in the field of implementation science." The gap in knowledge is even greater for low-resource contexts, as few studies have focused on these settings. This project aims to address this gap by developing and testing sustainment strategies for an evidenced-based youth suicide prevention program in a low-resource, American Indian (AI) contexts.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date April 24, 2024
Est. primary completion date October 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Knowledgeable about the implementation of the suicide prevention program - Over the age of 18 - Available to participate in required study meetings and assessments - Fluent in English Exclusion Criteria: - Factors identified at baseline that preclude full participation including: being under the influence of a substance; active psychosis or mania; any other condition that makes an individual lack capacity to give consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Sustainability strategies
The investigators will work with each site to determine strategies that are relevant locally to help promote sustainability of the suicide prevention program.

Locations

Country Name City State
United States Online Survey Whiteriver Arizona

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins Bloomberg School of Public Health National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Program Sustainability Assessment Tool Tool that assess domains of capacity for sustainability up to 5 years
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