Virtual Continuity and Its Impact on Complex Hospitalized Patients' Care
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT01397253 |
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Recruitment Status :
Completed
First Posted : July 19, 2011
Results First Posted : March 25, 2015
Last Update Posted : April 16, 2015
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Automated Communication Tools Complex Medical Patients | Other: Automated communication tools | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 835 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Health Services Research |
| Official Title: | Virtual Continuity and Its Impact on Complex Hospitalized Patients' Care |
| Study Start Date : | August 2010 |
| Actual Primary Completion Date : | January 2013 |
| Actual Study Completion Date : | January 2013 |
| Arm | Intervention/treatment |
|---|---|
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No Intervention: (Usual) MedTrak system of PCP notification
MedTrak, the information system used by the University of Pittsburgh Medical Center (UPMC), currently notifies PCPs when patients are admitted and discharged from the hospital.
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Experimental: Automated communication tools
An enhanced version of MedTrak (the present system of PCP notification). Electronic medical record links will be developed and used to allow automated communication with the PCP.
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Other: Automated communication tools
Automated communication tools will include:
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- Medication Errors at Hospital Discharge [ Time Frame: Approximately 1-30 days ]Medication name, dose, and frequency of administration for patient pre-admission medications will be recorded. Medications received during the hospitalization and discharge medications will be obtained by medical record review following hospital discharge. Pre-admission medications will be compared to discharge medications and differences will be considered discharge medication variances. Two trained pharmacists will independently review medication variances to determine clinical indications or medication errors.
- Patient PCP Visits, Emergency Room Visits and Rehospitalizations Within 30 Days Post-discharge. [ Time Frame: Within 30 post-discharge from hospital ]Details regarding patient PCP follow-up office appointments, ER visits and rehospitalizations occuring within 30 days post-discharge will be collected from the EMR.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Are admitted to UPMC Presbyterian General Medicine, Geriatrics, Cardiology, or Surgery inpatient services;
- Are 18 years of age or older;
- Are currently receiving 5 or more medications;
- Have 2 or more comorbid conditions present, defined using the Elixhauser comorbidity system (Med Care 1998;36:8-27 and Med Care. 2005 Nov; 43(11): 1130-9 ). These comorbidities are: congestive heart failure, cardiac arrhythmias, valvular disease, pulmonary circulation disorders, peripheral vascular disorders, hypertension, paralysis, other neurologic disorders, chronic pulmonary disease, diabetes uncomplicated, diabetes complicated, hypothyroidism, renal failure, liver disease, peptic ulcer disease excluding bleeding, AIDS/HIV disease, lymphoma, metastatic cancer, solid tumor without metastasis, rheumatoid arthritis/collagen vascular diseases, coagulopathy, obesity, weight loss, fluid and electrolyte disorders, blood loss anemia, deficiency anemias, alcohol abuse, drug abuse, psychoses, and depression
- Have a Primary Care Physician who has outpatient data included on EPIC electronic health record.
Exclusion Criteria:
- Are admitted to critical care units;
- Are admitted from skilled nursing facilities;
- Have dementia;
- Were previously enrolled in the study
- Are organ transplant recipients
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01397253
| United States, Pennsylvania | |
| UPMC Presbyterian Hospital | |
| Pittsburgh, Pennsylvania, United States, 15213-2582 | |
| Principal Investigator: | Kenneth J Smith, MD, MS | University of Pittsburgh Medical Center, University of Pittsburgh |
| Responsible Party: | University of Pittsburgh |
| ClinicalTrials.gov Identifier: | NCT01397253 |
| Other Study ID Numbers: |
3130920 |
| First Posted: | July 19, 2011 Key Record Dates |
| Results First Posted: | March 25, 2015 |
| Last Update Posted: | April 16, 2015 |
| Last Verified: | March 2015 |
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Automated Communication Tools Medication errors PCP communication |

