Targeted Infection Control in Long-term Care
Completed · Not applicable
Conditions studied: Infection
In brief
This is an interventional study aimed at reducing multi-drug resistance and infections in nursing home (NH) residents. Each year, a staggering 1.5-2.0 million infections occur in NHs. Many of these infections are caused by multiple drug resistant organisms (MDROs) including methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), and multidrug resistant Gram-negative bacilli (R-GNB). Antimicrobial resistance among common bacteria are adversely affecting the clinical course and exponentially increasing healthcare costs. Recognizing a need for action, legislators, policy makers, and consumer groups are advocating for pathogen-based universal preemptive screening for these MDROs, particularly MRSA in hospitals and NHs. However, implementing this sweeping mandate is controversial, costly, reactive, and not based on empirical evidence. It can result in a 10-20-fold increase in the number of NH residents placed in isolation precautions with the potential for reduced attention by healthcare workers, isolation and functional decline. The investigators proposal evaluates a novel focused approach between 'do nothing' and 'search all and destroy' strategies by targeting a subgroup of NH residents with indwelling devices who are at a high risk of acquiring MDROs and infections. The investigators hypothesize that the investigators targeted infection control program (TIP) will reduce MDRO colonization and infections in NH residents with indwelling devices. This cluster randomized trial will involve 12 NHs; 6 will be randomized to the TIP arm and 6 to the routine care arm. The investigators TIP intervention will include four components.
Key facts
- Study ID
- NCT01062841
- Run by
- University of Michigan
- People needed
- 418
- Starts
- 2010-05-01
- Expected to finish
- 2013-04-01
- Last updated by the study team
- 2016-09-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Any short- or long-stay resident with an indwelling urinary catheter or feeding tube for more than 72 hours
- Ability to get informed consent from either the resident or his/her durable power of attorney
You may not qualify if…
- Having an indwelling device for less than 72 hours
- Refusal of consent to get surveillance cultures and data collection by the resident or his/her durable power of attorney
- Residents who are receiving end-of-life care
Where it is running
- University of Michigan and partner nursing homes — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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