- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03034369
Caring for the Whole Person
Caring for the Whole Person: A Patient-Centered Assessment of Integrated Care Models in Vulnerable Populations
Study Overview
Status
Conditions
Intervention / Treatment
- Other: Access to Care
- Other: Depression Screening
- Other: Patient-Provider Relationship
- Other: Patient-Clinic Interactions
- Other: Stigma
- Other: Provider Continuity
- Other: Symptom Severity
- Other: Diagnoses
- Other: Social support
- Other: Preventive Screening
- Other: Inpatient Hospitalization Utilization
- Other: Inpatient Readmissions
- Other: Post-Admission follow-up
Detailed Description
Twelve safety net clinics have been selected to be a part of this study. The clinics vary on a BHI continuum level, which includes minimal collaboration, basic collaboration at a distance, basic collaboration on site, close collaboration (partially integrated) and close collaboration (fully integrated).
Twelve-thousand patients will be randomly selected from the 12 clinics to be invited to participate in the study. Patients who elect to participate will complete a survey at baseline to collect patient-reported outcomes and again twelve months later.
The Oregon All Providers All Claims (APAC) database will be accessed to analyze financial data regarding the patients at baseline and 12 months.
The hypothesis is that the degree of clinic BHI will predict patient outcomes.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
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Oregon
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Portland, Oregon, United States, 97213
- Center for Outcomes Research and Education, Providence Health & Services
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age >= 18
- Received care at a safety net care clinic in Oregon
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
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.
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Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with access to care.
Analysis of health care claims data for depression screenings at baseline and 12 months.
Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with patient-provider relationship.
Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with patient-clinic interactions.
Patient reported outcome survey administered at baseline and 12 months to measure perceived stigma.
Patient reported outcome survey administered at baseline and 12 months to measure satisfaction with provider continuity.
Patient reported outcome survey administered at baseline and 12 months to measure symptom severity.
Patient reported outcome survey administered at baseline and 12 months to measure diagnoses.
Patient reported outcome survey administered at baseline and 12 months to assess social support and outlets.
Analysis of health care claims data for preventive screenings at baseline and 12 months.
Analysis of health care claims data for Inpatient Hospitalization Utilization at baseline and 12 months.
Analysis of health care claims data for Inpatient Hospitalization Readmissions at baseline and 12 months.
Analysis of health care claims data for Post-Admission follow-up at baseline and 12 months.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in patient reported outcomes
Time Frame: 12 months
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Change in patient reported outcomes at baseline and 12 months
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12 months
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Change in health care claims
Time Frame: 12 months
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change in health care claims at baseline and 12 months
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12 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Bill J. Wright, PhD, Director, Center for Outcomes Evaluate and Education, Providence Health & Services
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 14-247A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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