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Trial to Reduce Antimicrobial Use in Nursing Home Residents With Alzheimer's Disease and Other Dementias 2.0 (TRAIN-AD 2)

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Hebrew SeniorLife

Status

Enrolling

Conditions

Alzheimer Disease
Infections
Dementia

Treatments

Behavioral: TRAIN AD 2.0

Study type

Interventional

Funder types

Other

Identifiers

NCT05950607
NIA R37AG032982

Details and patient eligibility

About

The goal of this pragmatic cluster randomized clinical trial is to compare management of suspected infection in nursing home residents with dementia The main questions it aims to answer whether residents with dementia in nursing homes randomized to use a multicomponent intervention to optimize suspected infection management ( versus usual care) use less antibiotics and fewer burdensome interventions.

Full description

This 52-month study (8 months preparation; 34 months trial conduct; 10 months data analyses and manuscript preparation)is a parallel cluster ePCT of an intervention to improve infection management for suspected infections among residents with moderate to advanced dementia (N=600; N=300/arm) living in NHs (N=50; N=25/arm). Facilities are members of a provider managed care network, Iowa Health Care Quality Network ('Network'). The intervention will be similar to the original TRAIN-AD program, but adapted for moderate to advanced dementia and rolled out in the Network. At each intervention NH, the intervention will be implemented for 24-months. Control NHs will employ usual care. In all NHs, there will be a 2-month startup period, 12-month resident enrollment period, and 24-months data collection period (Figure 2). Eligible residents with dementia will be identified using the EHR and Minimum DataSet (MDS) and followed up to 12 months. Outcome data will be ascertained from the EHR. Randomization and program roll out will be at the facility level. Analyses at the resident level. Clinical outcomes compared between arms at 12 months will be: 1. Antimicrobial courses/person-year in residents with moderate to advanced dementia (primary outcome) and all residents with dementia (secondary outcome) (Aim 1); and 2. Number of burdensome procedures/person-year used to manage suspected infections among residents with moderate to advanced dementia and those at all stages of dementia including: hospital transfers, urine specimens, chest x-rays, and blood cultures (secondary outcomes) (Aim 2). A process evaluation of implementation will be conducted in the intervention arm based on the RE-AIM framework1 (Aim 3) using quantitative and qualitative data (stakeholder interviews).

Enrollment

750 estimated patients

Sex

All

Ages

60 to 106 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age > 60
  2. A diagnosis of dementia (any type)
  3. Cognitive Functional Scale (CFS) > 1
  4. NH length of stay >90 days

The CFS score categorizes cognitive impairment status based on data in the electronic health record into: 1. None, 2. Mild, 3. Moderate, and 4. Severe (advanced). For the primary outcome, the analysis will be restricted to residents with a CFS score of 3 or 4.

Exclusion criteria

  1. Less than 60 years of age
  2. Living in nursing home for less than 90 days
  3. Does not have diagnosis of dementia
  4. Does not meet CFS >1 score

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

750 participants in 2 patient groups

TRAIN AD 2.0
Experimental group
Description:
Nursing homes randomized to the experimental arm will emply a multicomponent intervention among their providers designed to improve the management of suspected infections in residents with dementia. The components include: a.Orientation sessions for providers, b.On-line case based course for providers, c.Infection management algorithms for providers, d. Guidelines for providers to communicate with proxies, and e. Education booklet about infections in dementia for providers.
Treatment:
Behavioral: TRAIN AD 2.0
Usual Care
Active Comparator group
Description:
Nursing homes randomized to the conrol arm will employ usual care to manage nursing home residents with dementia with suspected infections.
Treatment:
Behavioral: TRAIN AD 2.0

Trial contacts and locations

1

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Central trial contact

Susan Mitchell, MD, MPH

Data sourced from clinicaltrials.gov

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