0BPROJECT SUMMARY/ABSTRACT
This project will create two complementary quality measures focused on pediatric anxiety. Pediatric anxiety
disorders are the extremely prevalent and rates are rising rapidly. Without effective treatment, anxiety
disorders can lead to more severe anxiety, depression, and substance use. Moreover, unresolved anxiety
disorders can have profound effects on functioning into adulthood and increase the risk for depression,
suicide, and chronic medical disorders. Although pediatric anxiety interventions, such as cognitive behavioral
therapy and antidepressant medications, are highly efficacious, many clinicians are under-using these
evidence-based treatments. An outcome-focused anxiety quality measure would provide a new tool for
improving the quality of pediatric anxiety treatment. By comparing aggregate casemix-adjusted anxiety
treatment outcomes among clinicians, clinics, and populations, organizations could identify opportunities for
quality improvement.
An obstacle to creating outcome-focused mental health measures in the United States has been the
absence of a practical way to collect, aggregate, and report mental health symptoms/functioning on
thousands of patients before and after treatment. We will develop and test two complementary casemix-
adjusted pediatric anxiety outcome quality measures using the GAD-7: (1) a measure of whether patients are
responding to treatment (treatment response), and (2) a whether patients’ anxiety remitted, which should be
feasible to implement at scale. Our specific aims are as follows:
Aim 1. Develop and test two complementary casemix-adjusted pediatric anxiety symptom quality measures.
Aim 2. Assess whether there are differences in anxiety outcomes by race, ethnicity, and social risk factors.
Aim 3. Determine how the measure will be implemented and used for quality improvement (feasibility and
usability).
Aim 4. Submit the quality measures for endorsement.
The GAD-7 is a widely used seven-item anxiety questionnaire that is psychometrically reliable, valid, and
responsive to change in pediatric and adult samples. Critically, the GAD-7 is easy for both specialty and
primary care providers to incorporate into their daily workflow and captures the primary symptoms of most
prevalent anxiety disorders, thus overcoming the main challenge to outcome-based mental health quality
measures. Large mental health systems in England, and more recently in Norway, Australia, and Northern
Ireland already use remission and response measures based on the GAD-7 to monitor outcomes on
thousands of pediatric patients with anxiety to inform quality improvement efforts.
Public Health Relevance Statement
PROJECT NARRATIVE
Anxiety disorders among youth are extremely common and without effective treatment can lead to depression,
substance use, suicide, and deficits in functioning into adulthood. Although pediatric anxiety interventions, such
as cognitive behavioral therapy and antidepressant medications, are highly efficacious, many clinicians are
under-using these evidence-based treatments. We will develop and test two complementary casemix-adjusted
pediatric anxiety outcome quality measures using the GAD-7 instrument: (1) a measure of whether patients are
responding to treatment (treatment response) and (2) a whether patients’ anxiety remitted (remission), which
will provide a critical tool for improving outcomes from anxiety treatment.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AdultAftercareAgeAnxietyAnxiety DisordersAustraliaCaliforniaCaringCase MixesCase-Mix AdjustmentsChildhoodChronicClinicCognitive TherapyComputerized Medical RecordDataDatabasesDevelopmentDiseaseDisease remissionEnglandEthnic OriginEvidence based treatmentFoundationsGoalsHealthHealth systemHealthcare SystemsHospitalsInternationalInterventionInterviewInvestmentsLinkMeasurementMeasuresMedicalMental DepressionMental HealthMental Health ServicesMonitorNational Institute of Mental HealthNorthern IrelandNorwayOutcomeOutcome MeasurePathological anxietyPatientsPharmaceutical PreparationsPopulationProcessProviderPsychometricsQuestionnairesRaceReportingResearchResourcesRiskRisk FactorsSamplingSuicideSymptomsTestingTimeTreatment outcomeUnited StatesValidationVendorYouthanti-depressive agentsanxiety symptomsanxiety treatmentcase controlchildhood anxietyeffective therapyelectronic medical record systemethnic minority populationhealth planimplementation barriersimprovedimproved outcomeindexinginstrumentmedical specialtiespatient populationpediatric patientsprimary care clinicianprimary care providerracial minorityresponsesocialsocial health determinantssubstance usetooltreatment of anxiety disorderstreatment responseusability
No Sub Projects information available for 1R01MH137006-01
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1R01MH137006-01
Patents
No Patents information available for 1R01MH137006-01
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1R01MH137006-01
Clinical Studies
No Clinical Studies information available for 1R01MH137006-01
News and More
Related News Releases
No news release information available for 1R01MH137006-01
History
No Historical information available for 1R01MH137006-01
Similar Projects
No Similar Projects information available for 1R01MH137006-01