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Electronic Consultation for AD/ADRD Residents Experiencing Infectious Diseases

Electronic Consultation for AD/ADRD Residents Experiencing Infectious Diseases

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04812769
Acronym
eCARE-ID
Enrollment
0
Registered
2021-03-24
Start date
2022-04-30
Completion date
2022-04-30
Last updated
2021-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Dementia, Antibiotics, Dementia, Nursing Homes

Brief summary

Pilot study to evaluate the feasibility of a pilot embedded pragmatic cluster randomized controlled trial to reduce the duration of antibiotic therapy and number of antibiotic prescriptions in nursing home residents with AD/ADRD.

Detailed description

The overall objective of the proposed investigation is to assess the feasibility of a pilot embedded pragmatic cluster randomized controlled trial (ePCT) to reduce the duration of antibiotic therapy and number of antibiotic prescriptions among nursing home residents with AD/ADRD. With the support of three independently owned and operated nursing homes that are unaffiliated with an academic medical center, we have developed the multicomponent intervention, eCARE-ID (Electronic Consultation for AD/ADRD Residents Experiencing Infectious Diseases). eCARE-ID consists of three components: 1) Tele-ID video clinical consultation services for nursing home residents; 2) electronic consultation (e-consultation) services for healthcare personnel at participating nursing homes; and 3) Tele-ID video antibiotic stewardship services for healthcare personnel including pharmacists at participating nursing homes.

Interventions

DEVICEeCARE-ID

The intervention, eCARE-ID, consists of: 1) telehealth video clinical consultation services for nursing homes residents; 2) electronic consultation services for healthcare personnel; 3) telehealth video antibiotic stewardship services for healthcare personnel

OTHERStandard of Care

Standard of care will be delivered to the control home.

Sponsors

Advarra
CollaboratorINDUSTRY
National Institute on Aging (NIA)
CollaboratorNIH
Brown University
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Two participating nursing homes will be assigned to the intervention. One participating nursing home will serve as a control.

Eligibility

Sex/Gender
ALL
Age
65 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

- residence in a participating nursing home

Exclusion criteria

\- Not willing to consent to the study

Design outcomes

Primary

MeasureTime frameDescription
Duration of antibiotic therapy in nursing home residents6 monthsThe primary outcome will be defined as the duration of antibiotic therapy in nursing home residents with AD/ADRD, measured as the total days of antibiotic therapy per 1000 resident-days among residents with ADRD.

Secondary

MeasureTime frameDescription
Number of antibiotic prescriptions in nursing home residents6 monthsThe secondary outcome will be defined as the number of antibiotic prescriptions in nursing home residents with AD/ADRD, defined as the total number of antibiotic prescriptions per 1000 resident-days among residents with AD/ADRD.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026