Viewing Study NCT00259454



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Study NCT ID: NCT00259454
Status: COMPLETED
Last Update Posted: 2010-03-16
First Post: 2005-11-28

Brief Title: Project COPEManaging Dementia at Home
Sponsor: Thomas Jefferson University
Organization: Thomas Jefferson University

Study Overview

Official Title: Managing Problem Behaviors of Alzheimers Disease
Status: COMPLETED
Status Verified Date: 2010-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study tests the effectiveness of an in-home intervention to reduce upset and burden among family caregivers and decrease nursing home placement The main hypothesis that will be tested is that compared to control group subjects experimental group participants will have enhanced well-being and fewer nursing home placements
Detailed Description: Implement a multi-component in-home intervention designed to prevent and ameliorate the troublesome behaviors that families typically confront and that often trigger nursing home placement The intervention combines the most effective strategies that have been identified in previous caregiver research by the investigative team and best clinical practices to provide a comprehensive service approach to families and individuals with dementia including education skills training home safety and stress management To enhance its applicability to real-world practice within the aging service network the intervention is designed to be reproducible and its components and treatment goals commensurate with the Medicaid Waiver Program In the absence of evidence-based service protocols currently in place for this Waiver population the intervention if effective would provide a systematic evidence-based approach in the Medicaid Waiver program to help families and persons with dementia remain at home and in their communities

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None