Reducing Behavioral and Psychological Symptoms of Dementia: Family Caregivers (Aim 1)

NACompletedINTERVENTIONAL
Enrollment

158

Participants

Timeline

Start Date

February 3, 2020

Primary Completion Date

December 29, 2021

Study Completion Date

December 29, 2021

Conditions
Alzheimer's Disease and Related Dementias
Interventions
BEHAVIORAL

PES-4-BPSD Model

We will conduct a non-randomized preliminary efficacy trial, enrolling N=158 patients (79 control and 79 intervention). The primary outcome will be presence of BPSD as measured by a patient's total score on the Neuropsychiatric Inventory-Questionnaire (NPI-Q) during hospitalization. A multi-modal approach (including chart review and HCG questionnaires) will be used to determine the presence and severity of BPSD.

BEHAVIORAL

The attention control condition

On this unit, the management of patients who display BPSD is performed by nurse assistants, rather than PES. Therefore, in order to test the added layer of PES staff, the nurse assistants on the control unit will receive equivalent dementia care education and training as well as staff support (please refer to NCT# 04179721 for more details on this aim).

Trial Locations (2)

11030

North Shore University Hospital, Manhasset

11040

Long Island Jewish Medical Center, Glen Oaks

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

National Institute of Nursing Research (NINR)

NIH

collaborator

Penn State University

OTHER

lead

Northwell Health

OTHER

NCT04481568 - Reducing Behavioral and Psychological Symptoms of Dementia: Family Caregivers (Aim 1) | Biotech Hunter | Biotech Hunter