RecruitingNot applicableNCT06151158
Preventing Suicidal Behavior With Diverse High-Risk Youth in Acute Care Settings
Studying Infantile neuroaxonal dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Johns Hopkins University
- Principal Investigator
- Holly C Wilcox, PhDJohns Hopkins Bloomberg School of Public Health
- Intervention
- Stanley Brown Safety Planning Intervention and Follow-up Contacts (SPI+)(behavioral)
- Enrollment
- 1000 target
- Eligibility
- 12-24 years · All sexes
- Timeline
- 2025 – 2028
Study locations (6)
- Johns Hopkins All Children's Hospital, St. Petersburg, Florida, United States
- Johns Hopkins University, Baltimore, Maryland, United States
- Columbia University Irving Medical Center (CUMC), New York, New York, United States
- Weill-Cornell Medicine, New York, New York, United States
- University of North Carolina Medical Center, Chapel Hill, North Carolina, United States
- Childrens Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Collaborators
Johns Hopkins All Children's Hospital · Children's Hospital of Philadelphia · Reichman University · Patient-Centered Outcomes Research Institute · Columbia University
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT06151158 on ClinicalTrials.govOther trials for Infantile neuroaxonal dystrophy
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