Web Platform to Integrate Behavioral Health

August 28, 2018 updated by: Medical Decision Logic, Inc.
Under this Small Business Innovation Research (SBIR) Phase II project, Research Topic 155, the Contractor will create an integrated multi-module system of web software tools to aid in behavioral health screening, prevention, triage, and tracking in medical, school, and mental health settings.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Health care systems experience problems with lack of tools, lack of knowledge, process variation, and system fragmentation in addressing behavioral health. As an ongoing science-based process for improving care and lowering costs, robust increases in translational capability are needed to re-tool health delivery systems for behavioral health integration. A logic linking translational capability to behavioral health integration as an ongoing shared information process, founded on the core belief that enabling human action with new information technology tools can grow knowledge, is the most powerful way to solve problems and improve health care.

Given these connected and interacting issues and obstacles, the Contractor has developed a solution strategy, building on four tiers of prior innovation and validation:

  • The Behavioral Health Screen (BHS);
  • BH-Works: the web software delivery of the BHS and new production features from Phase I;
  • BH-Works Portal: new production software features from Phase I; and
  • BH-Works Services: expertise and professional services to help primary care providers and healthcare systems integrate behavioral health into their organizations and workflows.

Study Type

Observational

Enrollment (Anticipated)

16000

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

    • Indiana
      • Connersville, Indiana, United States, 47331
        • Fayette Regional
    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19134
        • Port Richmond Family Medicine

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients that enter the health system through primary care clinics, academic medical and behavioral health centers, hospitals, or rural health clinics.

Description

Inclusion Criteria:

  • Potential Mental Health issue

Exclusion Criteria:

  • Not Willing to be Screened for mental health issues

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
Intervention / Treatment
Temple Physicians Incorporated
A community-based provider, operating 32 primary care sites
multi-module system of web software tools
WhiteBark
For profit entity created by the Indiana Rural Health Association
multi-module system of web software tools
Drexel Family Intervention Science
Academic center that developed and deployed Attachment Based Family Therapy (ABFT) assessment, treatment, and prevention models with an interest in adolescents struggling with substance abuse, depression, trauma, and suicidality.
multi-module system of web software tools
Bon Secours Health System
A primary care clinic in Baltimore that provides care services to a population in a lower socioeconomic status in downtown Baltimore.
multi-module system of web software tools
Howard University Hospital CARES
A project provides free outpatient medical, dental, mental health, nutrition and social services for HIV positive uninsured and underinsured residents of the District of Columbia.
multi-module system of web software tools

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Increase Provider Integration
Time Frame: 2 Years
Increase collaboration between Primary Care Physician and mental health series.
2 Years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Increase Screening
Time Frame: 2 Years
Increase identification rates of adults with depression and substance abuse problems.
2 Years
Increase Referrals
Time Frame: 2 Years
Increase successful referrals to mental health services.
2 Years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Allen Tien, MD, Medical Decision Logic, Inc.

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 (Anticipated)

September 25, 2018

Primary Completion (Anticipated)

September 25, 2019

Study Completion (Anticipated)

September 25, 2019

Study Registration Dates

First Submitted

November 20, 2017

First Submitted That Met QC Criteria

November 20, 2017

First Posted (Actual)

November 22, 2017

Study Record Updates

Last Update Posted (Actual)

August 29, 2018

Last Update Submitted That Met QC Criteria

August 28, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • N44DA-17-5679

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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