Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT06559774

The Hastiin Bidziil (Strong Man) Intervention

Led by Johns Hopkins Bloomberg School of Public Health · Updated on 2026-05-14

160

Participants Needed

2

Research Sites

154 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

The Hastiin Bidziil (Strong Man) Intervention

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 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)
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Navajo Nation Center for Indigenous Health - Chinle

Chinle, Arizona, United States, 86503

Actively Recruiting

2

Navajo Nation Center for Indigenous Health - Fort Defiance

Fort Defiance, Arizona, United States, 86504

Actively Recruiting

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Research Team

K

Kyann Dedman-Cisco, MPH

CONTACT

M

Marissa Begay, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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