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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)

Primary Purpose

Dementia, Alzheimer Disease, Infections

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
TRAIN AD 2.0
Sponsored by
Hebrew SeniorLife
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Dementia

Eligibility Criteria

60 Years - 106 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age > 60 A diagnosis of dementia (any type) Cognitive Functional Scale (CFS) > 1 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: Less than 60 years of age Living in nursing home for less than 90 days Does not have diagnosis of dementia Does not meet CFS >1 score

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    TRAIN AD 2.0

    Usual Care

    Arm 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.

    Nursing homes randomized to the conrol arm will employ usual care to manage nursing home residents with dementia with suspected infections.

    Outcomes

    Primary Outcome Measures

    Antimicrobial use in residents with moderate to advanced dementia
    Number of antimicrobial courses/person-year among residents with moderate to advanced dementia.

    Secondary Outcome Measures

    Antimicrobial use in residents with dementia
    Number of antimicrobial courses/person-year among residents with dementia at any stage.
    Burdensome interventions in residents with moderate to advanced dementia
    Number of burdensome interventions (hospital transfers, bladder catheterization, chest x-ray, blood cultures) used to evaluate suspected infections/person-year among residents withmoderate to advanced dementia.
    Burdensome interventions in residents with dementia
    Number of burdensome interventions (hospital transfers, bladder catheterization, chest x-ray, blood cultures) used to evaluate suspected infections/person-year among residents with dementia.

    Full Information

    First Posted
    July 10, 2023
    Last Updated
    July 10, 2023
    Sponsor
    Hebrew SeniorLife
    Collaborators
    Brown University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05950607
    Brief Title
    Trial to Reduce Antimicrobial Use in Nursing Home Residents With Alzheimer's Disease and Other Dementias 2.0
    Acronym
    TRAIN-AD 2
    Official Title
    Trial to Reduce Antimicrobial Use In Nursing Home Residents With Alzheimer's Disease and Other Dementias 2.0 (TRAIN-AD 2.0)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 1, 2023 (Anticipated)
    Primary Completion Date
    June 30, 2026 (Anticipated)
    Study Completion Date
    June 30, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Hebrew SeniorLife
    Collaborators
    Brown University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.
    Detailed 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).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Dementia, Alzheimer Disease, Infections

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    750 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    TRAIN AD 2.0
    Arm Type
    Experimental
    Arm 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.
    Arm Title
    Usual Care
    Arm Type
    Active Comparator
    Arm Description
    Nursing homes randomized to the conrol arm will employ usual care to manage nursing home residents with dementia with suspected infections.
    Intervention Type
    Behavioral
    Intervention Name(s)
    TRAIN AD 2.0
    Intervention Description
    The study intervention is a multi-component training program targeting direct care providers and healthcare proxies for NH residents with moderate to advanced dementia intended to improve the management of urinary tract infections (UTIs) and lower respiratory tract infections (LRIs). The components include: A. Provider Orientation: At NH start-up and q2 months providers will be offered orientations sessions involving two 15-minute presentations, one focused on the background and rationale for the program and one focused on describing the program components. B. A case-based on-line course, "Infection Management in Moderate to Advanced Dementia," C. Posters and pocket cards for providers displaying algorithms guiding appropriate antimicrobial initiation for suspected UTIs and LRIs that integrate patient preferences, and D. Proxies of ALL residents in the facility will be sent a booklet related to infection management for persons with moderate to advanced dementia. .
    Primary Outcome Measure Information:
    Title
    Antimicrobial use in residents with moderate to advanced dementia
    Description
    Number of antimicrobial courses/person-year among residents with moderate to advanced dementia.
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    Antimicrobial use in residents with dementia
    Description
    Number of antimicrobial courses/person-year among residents with dementia at any stage.
    Time Frame
    12 months
    Title
    Burdensome interventions in residents with moderate to advanced dementia
    Description
    Number of burdensome interventions (hospital transfers, bladder catheterization, chest x-ray, blood cultures) used to evaluate suspected infections/person-year among residents withmoderate to advanced dementia.
    Time Frame
    12 months
    Title
    Burdensome interventions in residents with dementia
    Description
    Number of burdensome interventions (hospital transfers, bladder catheterization, chest x-ray, blood cultures) used to evaluate suspected infections/person-year among residents with dementia.
    Time Frame
    12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    60 Years
    Maximum Age & Unit of Time
    106 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age > 60 A diagnosis of dementia (any type) Cognitive Functional Scale (CFS) > 1 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: Less than 60 years of age Living in nursing home for less than 90 days Does not have diagnosis of dementia Does not meet CFS >1 score
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Susan Mitchell, MD, MPH
    Phone
    16172813669
    Email
    smitchell@hsl.harvard.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Susan Mitchell, MD, MPH
    Organizational Affiliation
    Hebrew SeniorLife
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

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