Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
264 participants
INTERVENTIONAL
2012-01-31
2021-02-28
Brief Summary
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The primary hypotheses to be tested are:
Hypothesis1: Interventions to Reduce Acute Care Transfers (INTERACT) implementation NHs will have a greater reduction in hospitalization rate than the control and monitoring only NHs during the 12-month implementation compared to a 12-month baseline period.
Hypothesis 2: Reductions in Medicare expenditures for hospitalizations in the INTERACT implementation NHs will be greater than the estimated costs of implementing the intervention.
Hypothesis 3: The effects of INTERACT on hospitalization rates will be greater among patients on the Medicare skilled benefit for post-acute care, than for long-stay patients.
Hypothesis 4: The effects of INTERACT on hospitalization rates will be greatest among those NHs with higher vs. lower intensity (fidelity) of implementing the program.
Hypothesis 5: There will be a greater reduction in measures of hospitalizations for conditions defined as "potentially preventable" than for other transfers and hospitalizations.
Hypothesis 6: Implementation of INTERACT will not be associated with worsening of relevant quality measures in the participating NHs.
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Detailed Description
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1\) INTERACT implementation NHs will have a greater reduction in hospitalization rates than the control and monitoring only NHs during the 12-month implementation compared to a 12-month baseline period; and 2) reductions in Medicare expenditures for hospitalizations in the INTERACT intervention NHs will exceed the estimated costs of implementing the intervention.
The specific aims of this project are to:
1. Determine the effectiveness of implementing the INTERACT quality improvement program in reducing hospitalization rates.
2. Calculate the differences in Medicare expenditures for hospitalizations between NHs implementing INTERACT, the usual care control group, and NHs in the monitoring hospitalization rates only group.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Immediate INTERACT implementation
INTERACT Quality improvement program training and implementation between APR 2013 and MAR 2014
INTERACT Quality improvement program
INTERACT training and implementation between APR 2013 and MAR 2014
Delayed intervention with reporting
Quarterly surveys/data reporting between APR 2013 and MAR 2014. They receive INTERACT training starting on MAR 2014.
Quarterly surveys/data reporting
The nursing homes are asked to complete quarterly surveys between APR 2013 to MAR 2014
Delayed intervention not reporting
No data collected from these nursing homes for one year since baseline. They receive INTERACT training starting on MAR 2014.
No interventions assigned to this group
Interventions
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INTERACT Quality improvement program
INTERACT training and implementation between APR 2013 and MAR 2014
Quarterly surveys/data reporting
The nursing homes are asked to complete quarterly surveys between APR 2013 to MAR 2014
Eligibility Criteria
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Inclusion Criteria
* MD, NP or PA available on-site at least 1/week
* Capable of Starting intravenous fluids
* Capable of Providing respiratory treatments
* Capable of Assessing oxygenation status by pulse oximetry
* \< 4 hrs turnaround time for STAT medications ("stat" is an abbreviation of the Latin word statim, meaning "immediately, without delay")
* \< 8 hrs. turnaround time for STAT laboratory tests
* \< 8 hrs. turnaround time for STAT X-rays
* Computers available for online staff training
* Strong support for participation from the facility administrator, director of nursing, and medical director, as well as corporate leadership (for NHs that are part of a corporate chain), as evidenced by a signed agreement before enrollment
* \> 10% 30-day readmission rates
Exclusion Criteria
* Having only private pay residents (no Medicare/Medicaid, no Medicare provider number).
* Participation in a project designed specifically to reduce acute care transfers or hospitalization rates (including federal demonstrations)
* Conducting more than one other major quality improvement or research project during the project period which would threaten their ability to fully participate in the trial.
* Specialize in Pediatrics (\> 30 % of patients in NHs are pediatric)
* Specialize in HIV (\> 30 % of patients in NHs are HIV)
* Specialize in Respiratory care with ventilator care (\>30% of patients in NH are in this category)
* Robust INTERACT implementation and/or very low hospitalization rate
* Located in a country outside USA
ALL
No
Sponsors
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National Institute of Nursing Research (NINR)
NIH
University of Minnesota
OTHER
Florida Atlantic University
OTHER
Responsible Party
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Principal Investigators
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Joseph G Ouslander, MD
Role: PRINCIPAL_INVESTIGATOR
Florida Atlantic University
Ruth M Tappen, EdD RN FAAN
Role: PRINCIPAL_INVESTIGATOR
Florida Atlantic University
Locations
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Florida Atlantic University, College of Medicine/College of Nursing
Boca Raton, Florida, United States
Countries
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References
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Tappen RM, Newman D, Huckfeldt P, Yang Z, Engstrom G, Wolf DG, Shutes J, Rojido C, Ouslander JG. Evaluation of Nursing Facility Resident Safety During Implementation of the INTERACT Quality Improvement Program. J Am Med Dir Assoc. 2018 Oct;19(10):907-913.e1. doi: 10.1016/j.jamda.2018.06.017. Epub 2018 Aug 11.
Kane RL, Huckfeldt P, Tappen R, Engstrom G, Rojido C, Newman D, Yang Z, Ouslander JG. Effects of an Intervention to Reduce Hospitalizations From Nursing Homes: A Randomized Implementation Trial of the INTERACT Program. JAMA Intern Med. 2017 Sep 1;177(9):1257-1264. doi: 10.1001/jamainternmed.2017.2657.
Ouslander JG, Naharci I, Engstrom G, Shutes J, Wolf DG, Rojido M, Tappen R, Newman D. Hospital Transfers of Skilled Nursing Facility (SNF) Patients Within 48 Hours and 30 Days After SNF Admission. J Am Med Dir Assoc. 2016 Sep 1;17(9):839-45. doi: 10.1016/j.jamda.2016.05.021. Epub 2016 Jun 24.
Related Links
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Related Info
Other Identifiers
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304897
Identifier Type: -
Identifier Source: org_study_id
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