- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01912430
Retrospective Data Analysis of VitalCare Targeted Population Management on Scott and White Chronically Ill Beneficiaries
July 30, 2013 updated by: Scott & White Health Plan
Retrospective Data Analysis of the Impact of Vital Care Targeted Population Management Upon a Matched Cohort of Scott and White Health Plan Beneficiaries
New payment methods such as Accountable Care Organization (ACO's) and medical homes facilitate are new models for providers to deliver cost effective, quality patient outcomes.
Integrated Care Coaching (ICC) is a healthcare delivery model combining telephonic interventions with an intelligent information technology platform that offered validated protocols and patient outcomes tracking.
Health Integrated, Inc. has developed a validated program of Integrated Care Coaching (ICC), which was branded as "VitalCare", and implemented with over 7,000 members of the Scott and White Health Plan in Texas, would reduce healthcare costs/achieve a return on investment (ROI), improve clinical outcomes, and be satisfying for participants.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A prospective, pre-post historical control design trial with a concurrent control group cost/satisfaction analysis with a retrospective clinical study was undertaken with adult, Scott and White Health Plan (SWHP) patients with chronic illnesses.
From 2007 to 2010, a total of 7,411 ICC and 10,148 control patients participated.
Variables were costs, return on investment (ROI), iterative Patient Health Questionnaire (PHQ)9 scores, and satisfaction.
Study Type
Interventional
Enrollment (Actual)
17559
Phase
- Not Applicable
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
-
-
Texas
-
Temple, Texas, United States, 76502
- Scott & White Health Plan
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years or older
- Having one or more of 21 chronic conditions, including those with depression and multiple chronic comorbidities.
Exclusion Criteria:
- Presence of Major Cancer, HIV, or ESRD in either the baseline or measurement periods
- Claims in excess of $100,000 in either baseline or intervention period.
- Claims for long term care or hospice in either baseline or intervention period.
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
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ICC (Integrated Care Coaching)
Received evidence-based, protocol-driven integrated care coaching intervention to improve chronic illness health outcomes (clinical, financial).
|
Other Names:
|
|
Experimental: Control Group
Matched cohort by age and chronic illness diagnoses - no intervention
|
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Return of Investment and Cost of Medical Care
Time Frame: 6 to 12 months
|
Primary outcomes were ROI and cost of medical care (including inpatient, outpatient, emergency room, office and other (ie, physical therapy).
ICC participants and control group members had a minimum of 6 months to a maximum of 12 months measurement period.
|
6 to 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Level of Depressive Symptoms per Interactive Patient Health Questionnaire (PHQ-9) scores
Time Frame: 6 to 12 months
|
Secondary outcome was level of depressive symptoms per Interactive Patient Health Questionnaire (PHQ-9) scores.
ICC participants and control group members had a minimum of 6 months to a maximum of 12 months measurement period.
|
6 to 12 months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Patient Satisfaction
Time Frame: 6 to 12 months
|
6 to 12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Marylou Buyse, M.D., M.S., Scott and White Health Plan
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
July 1, 2012
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
July 18, 2013
First Submitted That Met QC Criteria
July 29, 2013
First Posted (Estimate)
July 31, 2013
Study Record Updates
Last Update Posted (Estimate)
August 1, 2013
Last Update Submitted That Met QC Criteria
July 30, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 120246
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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