- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02390557
Persons With Disabilities Generating Quality Metrics
Persons With Disabilities Generating Quality Metrics to Inform Integrated Care
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aims of the project are as follows:
To work with persons with significant physical disabilities and serious and persistent mental illness to develop two new approaches to assess quality of care:
Approach #1: We will survey enrollees about their experiences in One Care and their thoughts about the care they receive. This survey will also ask One Care enrollees about how they manage their care and what self-direction means to them. The survey will be called the Persons with Disabilities Quality Survey (PDQ-S), and it will be available in English and Spanish versions.
Approach #2: Enrollees in One Care will provide information about their perceptions of care quality to a trained team of persons with disabilities who will report the information to One Care care teams. The goal of the activity is to support quality improvement in One Care through hearing the consumer's voice. This is called YES Health - Your Experience: Speak up for better health care.
- We want to test how providing consumer informed and consumer directed quality information to One Care providers affects One Care quality.
- We want to improve the ability of One Care enrollees to manage their own health care and to recognize and report quality problems
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- One Care enrollee
- Permanent physical disability and/or serious mental illness
- Seen at designated practice site
- English or Spanish speaking
Exclusion Criteria:
- Persons with an intellectual or a developmental disability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control - Standard Practice
Standard measures of quality at baseline.
No intervention reports sent to providers
|
|
Experimental: Survey
Persons with Disabilities Quality Survey.PDQS Survey Reports Intervention.reports
sent to providers of OneCare enrollees
|
PDQS survey reports only
|
Experimental: YESHealth
Arm 3: YESHealth Reports and PDQS Survey Reports sent to providers of OneCare enrollees
|
PDQS survey reports only
Arm 3: YESHealth and PDQS survey reports to providers
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improved Quality of Care
Time Frame: 12 months
|
% who agree that their quality of care Is better, the same or worse than before
|
12 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lisa I Iezzoni, MD, MSc, Mongan Institute Health Policy Center, Massachusetts General Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014000899
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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