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The Hastiin Bidziil (Strong Man) Intervention

The Hastiin Bidziil (Strong Man) Intervention: A Study to Measure the Effectiveness of a Secondary Prevention Program Aimed at Reducing Substance Use Among Adult Native Men

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06559774
Enrollment
160
Registered
2024-08-19
Start date
2025-06-18
Completion date
2028-06-01
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Use

Keywords

Young Men, Common Elements Treatment Approach (CETA)

Brief summary

The Hastiin Bidziil (Strong man) Intervention study is part of a larger project called, Community-Driven Indigenous Research, Cultural Strengths & Leadership to Advance Equity in Substance Use Outcomes (CIRCLE) Center of Excellence. CIRCLE aims to address drug use related health problems in collaboration with diverse Indigenous communities. This study is a randomized controlled trial study to measure the effectiveness of a secondary prevention program, called Hastiin Bidziil (Strong Man), aimed at reducing substance use among Native American Indian (AI) men ages 18 years and older

Interventions

BEHAVIORALHastiin Bidziil

Common Elements Treatment Approach (CETA) modified for cultural and gendered specific delivery for maximum community impact

OTHERControl condition - vehicle maintenance

Control condition was selected by the Community Research Council and includes five sessions on basic vehicle maintenance such as changing tire, checking fluid levels, and winterizing vehicles.

Sponsors

Johns Hopkins Bloomberg School of Public Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Masking description

The co-Leads (project Investigators) are blinded to randomization status of participants.

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Self-identify as American Indian * Self-identify as a man * Age 18 years or older at time of enrollment * Screen positive for lifetime use of alcohol and/or drugs, except for tobacco use only * Reside within \~60 miles of a study community (Fort Defiance, AZ; Chinle, AZ)

Exclusion criteria

* Any condition that would affect successful participation (e.g., planned move) * Profound disability that limits the ability to participate in assessments or interventions * Participated in the preliminary phase of this study to adapt CETA for this project

Design outcomes

Primary

MeasureTime frameDescription
Number of days of substance sse as assessed by Time Line Follow-back8-months post baselineNumber of days of substance use over the previous month measured at 8-months post baseline using Timeline Follow-Back (TLFB)

Countries

United States

Contacts

CONTACTKyann Dedman-Cisco, MPH
kdedman1@jhu.edu928-674-6824
CONTACTMarissa Begay, MA
mbegay5@jhu.edu928-674-6824
PRINCIPAL_INVESTIGATORJennifer Richards, PhD

Johns Hopkins University

PRINCIPAL_INVESTIGATORJerreed D Ivanich, PhD

University of Colorado, Denver

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026