Improving Safety of Transitions to Skilled Nursing Care Using Videoconferencing (ECHO-CT)
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|ClinicalTrials.gov Identifier: NCT03832257|
Recruitment Status : Recruiting
First Posted : February 6, 2019
Last Update Posted : June 4, 2020
|Condition or disease||Intervention/treatment||Phase|
|Acute Disease||Other: ECHO CT Intervention Other: Matched Non-Participating Facilities||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||800 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||AHRQ Health Services Research Projects: Making Health Care Safer in Ambulatory Care Settings and Long Term Care Facilities|
|Actual Study Start Date :||September 30, 2018|
|Estimated Primary Completion Date :||August 31, 2021|
|Estimated Study Completion Date :||August 31, 2021|
Experimental: ECHO CT Intervention
Weekly video conference between hospitalist at Beth Israel and skilled nursing facilities.
Other: ECHO CT Intervention
weekly video conference between hospitalist and skilled nursing facilities
Matched Non- Participating Facilities
Matched non-participating facilities
Other: Matched Non-Participating Facilities
Matched Non-Participating Facilities
- 30-Day Readmission Rates [ Time Frame: 30-Days ]Number of hospital readmissions over 30 day period among participating SNF sites
- Health Care Utilization [ Time Frame: up to 90 days ]Includes average length of stay in the facility
- Incidence of Adverse Clinical Conditions [ Time Frame: 30 Days ]From the MDS (variable codes in parentheses), including rates of dehydration (J1550C), internal bleeding (J1550D), falls (J1800), anti-psychotic medication use (N0400A), delirium (C1300), surgical wound infections (I2500 and M1040E), pressure ulcers (M0210), and uncontrolled pain (J0850).
- Health Care Cost [ Time Frame: 30-days ]Total 30-day Medicare costs for fee-for-service patients.
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): NCT03832257
|Contact: Lewis Lipsitz, MD||617-971-5318||Lipsitz@hsl.harvard.edu|
|Contact: Lauren Junge-Maughan||617- email@example.com|