NCT03034369

Brief Summary

The goal of this study is to identify outcomes associated with Behavioral Health Integration (BHI) that matter to patients, to compare changes in outcome over time to measure the impact of different BHI models on different patients, and to create and maintain an Integration Learning Collaborative.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
6,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2015

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2015

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

January 25, 2017

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 27, 2017

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

June 15, 2017

Status Verified

June 1, 2017

Enrollment Period

2.8 years

First QC Date

January 25, 2017

Last Update Submit

June 13, 2017

Conditions

Keywords

IntegrationPrimary CareBehavioral HealthHealth Care ReformMedical HomeAccountable Care Organization

Outcome Measures

Primary Outcomes (2)

  • Change in patient reported outcomes

    Change in patient reported outcomes at baseline and 12 months

    12 months

  • Change in health care claims

    change in health care claims at baseline and 12 months

    12 months

Study Arms (1)

Safety Net Clinic Patients

A Cohort of patients in 12 different primary care clinics will be studied to measure how changes in different integration factors impacts the following patient reported outcomes at baseline and 12 months: Access to Care, Patient-Provider Relationship, Patient-Clinic Interactions, Stigma, Provider Continuity, Symptom Severity, Diagnoses, and Social Support. Health care claims data will be accessed to analyze Depression Screening, Preventive Screening, Inpatient Hospitalization Utilization, Inpatient Readmissions, and Post-Admission follow-up at baseline and 12 months.

Other: Access to CareOther: Depression ScreeningOther: Patient-Provider RelationshipOther: Patient-Clinic InteractionsOther: StigmaOther: Provider ContinuityOther: Symptom SeverityOther: DiagnosesOther: Social supportOther: Preventive ScreeningOther: Inpatient Hospitalization UtilizationOther: Inpatient ReadmissionsOther: Post-Admission follow-up

Interventions

Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with access to care.

Safety Net Clinic Patients

Analysis of health care claims data for depression screenings at baseline and 12 months.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with patient-provider relationship.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with patient-clinic interactions.

Safety Net Clinic Patients
StigmaOTHER

Patient reported outcome survey administered at baseline and 12 months to measure perceived stigma.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with provider continuity.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to measure symptom severity.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to measure diagnoses.

Safety Net Clinic Patients

Patient reported outcome survey administered at baseline and 12 months to assess social support and outlets.

Safety Net Clinic Patients

Analysis of health care claims data for preventive screenings at baseline and 12 months.

Safety Net Clinic Patients

Analysis of health care claims data for Inpatient Hospitalization Utilization at baseline and 12 months.

Safety Net Clinic Patients

Analysis of health care claims data for Inpatient Hospitalization Readmissions at baseline and 12 months.

Safety Net Clinic Patients

Analysis of health care claims data for Post-Admission follow-up at baseline and 12 months.

Safety Net Clinic Patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients accessing care at safety net clinic in Oregon.

You may qualify if:

  • Age \>= 18
  • Received care at a safety net care clinic in Oregon

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center for Outcomes Research and Education, Providence Health & Services

Portland, Oregon, 97213, United States

Location

Related Links

MeSH Terms

Interventions

Health Services Accessibility

Intervention Hierarchy (Ancestors)

Delivery of Health CarePatient Care ManagementHealth Services AdministrationHealth Care Quality, Access, and Evaluation

Study Officials

  • Bill J. Wright, PhD

    Director, Center for Outcomes Evaluate and Education, Providence Health & Services

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 25, 2017

First Posted

January 27, 2017

Study Start

March 1, 2015

Primary Completion

December 1, 2017

Study Completion

December 1, 2017

Last Updated

June 15, 2017

Record last verified: 2017-06

Data Sharing

IPD Sharing
Will not share

Locations