AdolCHICA: Improving Adolescent Health Outcomes Through Preventive Care Transformation

Sponsor
Indiana University (Other)
Overall Status
Completed
CT.gov ID
NCT02244138
Collaborator
Agency for Healthcare Research and Quality (AHRQ) (U.S. Fed)
2,831
1
37
76.6

Study Details

Study Description

Brief Summary

Preventive care for adolescents is vitally important for maximizing their health and well-being. Unfortunately, pediatric primary care frequently fails to meet the preventive needs of adolescents as demonstrated by poor health outcomes for this population.

In this grant application, the investigators propose to expand an existing computer decision support system (CDSS) into the investigators adolescent primary care practices for the purpose of implementing a comprehensive, and developmentally appropriate, screening and physician decision support process. Prior work completed by the investigators research group has demonstrated the feasibility of using CDSS to implement and evaluate clinical guidelines. The investigators seek to positively impact the effectiveness of preventative primary care visits by applying this previous success to the investigators adolescent practice. The investigators hypothesize that the implementation of developmentally appropriate universal screening practices, using tablet technology, and enhanced physician decision support regarding clinically relevant guidelines for all annual adolescent preventive care visits will result in better health outcomes, including higher rates of adherence to physician recommendations and improved patient functioning.

The specific research aims of this proposal are:

Aim 1: Expand and modify an existing CDSS to include an Adolescent Preventive Care Module comprised of developmentally appropriate screening tools for adolescents aged 11 to 21 years and tailored evidence-based clinical decision support for physicians.

Aim 2: Evaluate the impact of the Adolescent Preventive Care Module on the identification of specific mental and physical health problems and treatment outcomes in an adolescent primary health care setting.

Adolescent primary care issues of interest for this project include sexually transmitted infection (STI), depression, substance use and Human Papillomavirus (HPV) immunization. The investigators expect this project to improve the health outcomes of adolescents, guide future efforts to implement universal screening and CDSS in a variety of primary care settings, and provide additional evidence to support broad-based electronic screening and computerized decision support for use in preventive care as a method for improving adolescent health.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Adolescent CDSS

Study Design

Study Type:
Observational
Actual Enrollment :
2831 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Improving Adolescent Health Outcomes Through Preventive Care Transformation
Actual Study Start Date :
Sep 1, 2014
Actual Primary Completion Date :
Sep 30, 2017
Actual Study Completion Date :
Sep 30, 2017

Arms and Interventions

Arm Intervention/Treatment
Adolescent CDSS

Implementation clinic site for CDDS

Behavioral: Adolescent CDSS
computer decision support system (CDSS) for health care providers of adolescents in primary care

Outcome Measures

Primary Outcome Measures

  1. sexually transmitted infection [12 months]

    diagnosis of sexually transmitted infection by physician as indicated in electronic health record for patient

Secondary Outcome Measures

  1. depression [12 months]

    diagnosis of depression by physician as indicated in electronic health record for patient

Other Outcome Measures

  1. substance use [12 months]

    diagnosis of substance use by physician as indicated in electronic health record for patient

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 21 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 11-21 years

  • attending primary care clinic

Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Eskenazi Medical Group Indianapolis Indiana United States 46203

Sponsors and Collaborators

  • Indiana University
  • Agency for Healthcare Research and Quality (AHRQ)

Investigators

  • Principal Investigator: matthew c aalsma, phd, Indiana University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Matthew Aalsma, Associate Professor, Indiana University
ClinicalTrials.gov Identifier:
NCT02244138
Other Study ID Numbers:
  • 1308038999
  • R01HS022681
First Posted:
Sep 18, 2014
Last Update Posted:
Aug 9, 2018
Last Verified:
Aug 1, 2018
Keywords provided by Matthew Aalsma, Associate Professor, Indiana University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2018