Clinical Trials Directory

Trials / Completed

CompletedNCT01267682

Cognitive Intervention For Delirium in Dementia

Reserve For Delirium Superimposed On Dementia (DSD)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
283 (actual)
Sponsor
Penn State University · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to test the effectiveness of cognitively stimulating activities for resolving delirium in people with dementia.

Detailed description

The primary aim in this RCT is to test the efficacy of Recreational Stimulation for Elders as a Vehicle to resolve DSD (RESERVE- DSD). The investigators will randomize 256 subjects, newly admitted to post acute care, to intervention (RESERVE-DSD) or control (usual care). Intervention subjects will receive 30-minute sessions of tailored cognitively stimulating recreational activities for up to 30 days. The investigators hypothesize that subjects who receive RESERVE-DSD will have: decreased severity and duration of delirium; greater gains in attention, orientation, memory, abstract thinking, and executive functioning; and greater gains in physical function compared to subjects with DSD who receive usual care. The investigators will also evaluate potential moderators of intervention efficacy (lifetime of complex mental activities and APOE status). The secondary aim is to describe the costs associated with RESERVE-DSD.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCognitive StimulationThirty minutes of cognitive stimulation delivered daily for thirty minutes.

Timeline

Start date
2011-01-01
Primary completion
2016-01-01
Completion
2016-03-01
First posted
2010-12-28
Last updated
2016-09-27

Locations

9 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01267682. Inclusion in this directory is not an endorsement.