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National Child Traumatic Stress Network (NCTSN) Quality Improvement Initiative Database

National Child Traumatic Stress Network (NCTSN) Quality Improvement Initiative Database

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01591694
Enrollment
4193
Registered
2012-05-04
Start date
2012-04-30
Completion date
2017-02-07
Last updated
2018-04-06

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

Conditions

ADHD, Anxiety, Conduct Disorder, Depression, Post Traumatic Stress Disorder

Keywords

child trauma, maltreatment, physical abuse, sexual abuse, emotional abuse, abandonment, domestic violence, community violence

Brief summary

Trauma-informed treatment will improve emotional regulation and behavior.

Detailed description

The proposed study is to request permission to continue federally mandated data collection to examine the clinical outcomes of children at the Family Center at Kennedy Krieger Institute who are enrolled in evidence-based and promising trauma-informed treatments as part of the National Child Traumatic Stress Network funded by the Substance Abuse and Mental Health Services Administration. The purpose of the National Child Traumatic Stress Initiative(NCTSNI) Evaluation is to determine the extent to which the NCTSI, through the National Child Traumatic Stress Network (NCTSN), has raised the standard of care and improved access to services for traumatized children. In addition, the evaluation assesses the extent to which the NCTSI has served as a national resource capable of improving children's access to high-quality, trauma-informed mental health services. This data, previously collected and managed by the Category I NCTSN Center at Duke will now be managed by ICF Macro in a data system entitled NICON.

Interventions

None listed

Sponsors

Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Children enrolled in treatment at the Family Center and caregivers

Exclusion criteria

* Psychosis, * Inability to comply with directions

Design outcomes

Primary

MeasureTime frameDescription
Behavior1 yearImproved behavioral and emotional regulation, i.e., improved behavior compliance, improved misbehavior symptoms, reduced symptoms of anxiety, depression, attention deficit hyperactivity disorder (ADHD), conduct disorder, oppositional defiant disorder, and post traumatic stress syndrome (PTSD). Improved sleep, toileting, parent-child attachment, and mood regulation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026