- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02738320
Patient Centered Quality Reporting
April 8, 2016 updated by: Dana Mukamel, University of California, Irvine
The purpose of this study is to develop a consumer friendly web-based interface between Nursing Home Compare (NHC) and an e-coaching/decision-aid tool (NHCPlus) and determine if use of NHCPlus facilitates and enhances access to and use of NHC.
Study Overview
Study Type
Interventional
Enrollment (Actual)
225
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
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California
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Irvine, California, United States, 92697
- University of California
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-
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
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients who have been admitted as an inpatient into the departments of Medicine or Surgery at the UC Irvine Medical Center, and whose discharge plan is to a nursing home.
- Family members of these patients, if they are involved in the choice of nursing home, were also recruited to the study, either as joint decision makers with the patients or as proxy decision makers for the patient.
Exclusion Criteria:
- Patients less than 50 years of age.
- Patients unable to use NHCPlus technology or participate in the nursing home choice decision (i.e. non-English speaking, severely visual or hearing impaired, dementia, or other debilitating illnesses) will be excluded unless they have a representative/proxy who will be involved in the decision to select the nursing home.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Intervention
Intervention patients will receive access to NHCPlus when discharge to a nursing home from the hospital is expected.
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A decision-aid tool that will interface with Nursing Home Compare and improve consumers' ability to assimilate and incorporate the information into their process of choosing a nursing home.
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No Intervention: Usual Care
Control patients will receive the usual care when discharge to a nursing home from the hospital is expected.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Use of Nursing Home Compare information
Time Frame: up to 9 days post discharge
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Patients (or their families) self report their knowledge and use of the information in Nursing Home Compare.
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up to 9 days post discharge
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Quality Measures of chosen nursing home
Time Frame: up to 9 days post-discharge
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Quality measures obtained from the Nursing Home Compare web based report card
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up to 9 days post-discharge
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Distance between patient/family residence and the chosen nursing home.
Time Frame: up to 9 days post-discharge
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Driving distance between the patient zip code and the chosen nursing home zip code using Google maps.
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up to 9 days post-discharge
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Length of stay in hospital
Time Frame: between 1 and 68 days
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Number of days between admission date and discharge date
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between 1 and 68 days
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dana Mukamel, PhD, University of California
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
March 1, 2014
Primary Completion (Actual)
September 1, 2015
Study Completion (Actual)
November 1, 2015
Study Registration Dates
First Submitted
April 5, 2016
First Submitted That Met QC Criteria
April 8, 2016
First Posted (Estimate)
April 14, 2016
Study Record Updates
Last Update Posted (Estimate)
April 14, 2016
Last Update Submitted That Met QC Criteria
April 8, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- HS# 2012-9098
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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