Study Stopped
this study was determined by IRB not to be humans subjects research
Use of the Ask Suicide-Screening Questions (ASQ) in Pediatric Outpatient Settings
2 other identifiers
observational
525
1 country
2
Brief Summary
Background: Doctors and nurses who work in non-mental health settings need ways to know when patients are at risk. Researchers created the Ask Suicide-Screening Questions (ASQ) to be used in an emergency department for children. This is a 4-item suicide risk screening tool. We wanted to see if this is also a good tool to use in the outpatient setting. Two studies are being done to test it at hospitals. This study is for researchers to analyze the data from those two studies. Objectives: To combine and analyze data from two studies to see how well the ASQ can detect suicide risk in pediatric outpatient clinics. Eligibility: No people are enrolled in this study. Design: Participants in the two non-NIH studies will give consent for their data to be shared. The data will be confidential and secure. They will have no personal information attached to them. Researchers will get the data and analyze them.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2016
Typical duration for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 9, 2016
CompletedStudy Start
First participant enrolled
July 9, 2016
CompletedFirst Posted
Study publicly available on registry
July 12, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 10, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
April 22, 2020
CompletedApril 28, 2020
April 1, 2020
1.8 years
July 9, 2016
April 24, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Primary outcome measures include frequencies of positive responses to all ASQ and SIQ items.
Ongoing
Secondary Outcomes (1)
Responses to demographic survey items will allow us to describe if the primary outcome measure varies by race, gender, education level, and other demographic variables. A depression screen and a brief questionnaire to assess parent opinion will...
Ongoing
Eligibility Criteria
You may qualify if:
- Patient in the Adolescent/Young Adult Medicine Program.
- English-speaking
- Aged 10-21 years, inclusive.
- If 18 or older, can supply consent.
- If under 18, has a parent or legal guardian who is available for informed consent (written/verbal).
You may not qualify if:
- Has a severe developmental or cognitive delay.
- Has a severe communication disorder such that the patient cannot comprehend questions or communicate answers.
- Has a severe illness that prevents adequate communication.
- Parents/guardians and/or patients are non-English speaking.
- Patients under 18 years old are not with a parent/legal guardian who can provide written consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Childrens Hospital, Boston
Boston, Massachusetts, 02115, United States
The Childrens Mercy Hospital
Kansas City, Missouri, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lisa M Horowitz, Ph.D.
National Institute of Mental Health (NIMH)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 9, 2016
First Posted
July 12, 2016
Study Start
July 9, 2016
Primary Completion
May 10, 2018
Study Completion
April 22, 2020
Last Updated
April 28, 2020
Record last verified: 2020-04