- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00448331
Facilitated Referral for Children Screening Positive for Mental Illness (MI)
October 31, 2007 updated by: Children's Hospital Medical Center, Cincinnati
Facilitated Referral for Children Screening Positive for Mental Illness in the Pediatric Emergency Department and Readiness to Seek Care
The purpose of this study is to find out how prevalent unidentified Mental Health issues are in the pediatric population that visits the Emergency Department in an urban city.
Study Overview
Status
Completed
Detailed Description
The purpose of this research study is to find out how many children in the Emergency Room have emotional issues and how many of them go unnoticed.
In particular the study looks at how well a questionnaire for children and teenagers, the DISC Predictive Scales, Version IV (DPS-IV) works and what is the best way to ask the questions.
In addition, for children aged 9-17 this study will look at families' readiness to seek care when a problem is indicated.
Study Type
Observational
Enrollment (Actual)
551
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ohio
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Cincinnati, Ohio, United States, 45229
- Cincinnati Children's Hospital Medical Center Emergency Department
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Emergency Department patients ages 6-18 who present without any history of mental health issues.
Description
Inclusion Criteria:
- Child Must be With Biological Mother
- Child Presenting to Emergency Department with an Urgent But Stable condition
- Child must be between the ages of 6 years and 18 years
- Child must have no prior history of Behavioral Health concerns or diagnoses
Exclusion Criteria:
- Child has prior Behavioral Health history, diagnosis, or concerns
- Child not between ages of 6 years and 18 years of ages
- Child presenting without Biological Mother present
- Child acuity level outside of Urgent But Stable for presenting complaints
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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positive screen, negative screen
Positive screens are those who received positive feedback regarding their answers to a mental illness screening assessment.
Negative screens received feedback stating that they did not screen positive for any mental illness.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Jackie Grupp-Phelan, MD, MPH, Children's Hospital Medical Center, Cincinnati
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2004
Study Completion (ACTUAL)
August 1, 2007
Study Registration Dates
First Submitted
March 14, 2007
First Submitted That Met QC Criteria
March 14, 2007
First Posted (ESTIMATE)
March 16, 2007
Study Record Updates
Last Update Posted (ESTIMATE)
November 2, 2007
Last Update Submitted That Met QC Criteria
October 31, 2007
Last Verified
October 1, 2007
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 02-9-27
- MH063916-03
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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