Status:

COMPLETED

PACT: Providers and Alzheimer's Caregivers Together

Lead Sponsor:

National Institute on Aging (NIA)

Collaborating Sponsors:

National Institute of Nursing Research (NINR)

Conditions:

Alzheimer's Disease

Dementia

Eligibility:

All Genders

21+ years

Phase:

NA

Brief Summary

The primary goal of the study is documentation of effectiveness of a home-based intervention to reduce caregiver burden related to dementia caregiving, improve caregiver health status, and reduce care...

Detailed Description

This study focuses on an underserved, understudied population: African American and White homebound persons with dementia and their caregivers (CGs). Severe dementia, frailty, multiple disabling co-mo...

Eligibility Criteria

Inclusion

  • Care Recipient - Inclusion Criteria (must have all)
  • Documented diagnosis of dementia or Mini-Mental State Exam score \<23
  • Functional impairment: presence of two IADL (Instrumental Activities of Daily Living) impairment (transportation, shopping) or one Activities of Daily Living (ADL) impairment (bathing, toileting)
  • Caregiver - Inclusion Criteria (must have all)
  • At least 21 years old
  • A family member of the care recipient
  • Must have a telephone
  • Must plan to remain in the area for the duration of the intervention and follow-up
  • Must have been a caregiver for more than 6 months
  • Must provide at least 4 hours of supervision or direct assistance per day for the care recipient

Exclusion

  • Care Recipient
  • Any terminal illness with life expectancy of less than 6 months
  • Active treatment (chemotherapy or radiation therapy) for cancer
  • More than three acute medical hospitalizations in the past year (other than psychiatric or Alzheimer's Disease related admissions)
  • Schizophrenia
  • Dementia secondary to head trauma
  • Blindness or deafness if either disability prohibits them from data collection or participation in the interventions
  • Caregiver
  • Any terminal illness with life expectancy of less than 6 months
  • Active treatment (chemotherapy or radiation therapy) for cancer
  • More than three acute medical hospitalizations in the past year
  • Imminent placement of care recipient into a nursing home (within 6 months)
  • Involvement in another clinical trial for caregivers, including REACH
  • Miscellaneous barriers such as transportation, commitment, hesitancy, etc.

Key Trial Info

Start Date :

October 1 2000

Trial Type :

INTERVENTIONAL

End Date :

November 1 2005

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT00182897

Start Date

October 1 2000

End Date

November 1 2005

Last Update

November 14 2006

Active Locations (1)

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1

University of Tennessee Health Science Center

Memphis, Tennessee, United States, 38163