Reducing Behavioral and Psychological Symptoms of Dementia: Hospital Caregivers (Aim 2)
Alzheimer's Disease and Related Dementias
About this trial
This is an interventional health services research trial for Alzheimer's Disease and Related Dementias focused on measuring Behavioral and Psychological Symptoms of Dementia, Alzheimer's Disease and Related Dementias, Hospitalization
Eligibility Criteria
Inclusion criteria:
- All PES staff on the intervention unit and nursing assistant staff on the control unit will be approached by research coordinator who has no authoritative responsibilities, emphasizing voluntary participation
Exclusion criteria:
- Staff who decline to participate in the study
- Staff that are not permanently based on either the intervention or control units
Sites / Locations
- Long Island Jewish Medical Center
- North Shore University Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
The PES-4-BPSD Model
The attention control condition
The intervention arm consists of PES and NAs who work on the intervention unit which consists of: I. Cohorting of patients with cognitive impairment AND past or present indication of BPSD, acutely admitted to the medicine or telemetry service, are cohorted on a 10-bed medical unit. II. PES staff. III. Staff Support: The PI will hold monthly 20 minute group sessions to reinforce training and discuss challenging patient behaviors; meant to improve the attitude and empathy of hospital caregivers towards patients. IV. Staff Training
The control group consists of NAs that work on a 40-bed medicine unit, staffed with 39 nurses (1:6 ratio) and 26 NA (1:8 ratio), that primarily cohorts older patients with geriatric syndromes. All components of the intervention arm are the same with the exception of the PES staff. The control arm (NAs) will receive the same training as the intervention arm.