Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Memphis, Tennessee 38163


Purpose:

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 caregiver and care recipient resource utilization.


Study summary:

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-morbid diseases, lack of transportation, inability to afford or obtain a sitter for the care recipient (CR), and lack of time in a CG's burdened daily schedule may prevent care dyads (caregivers and their family member with dementia) from receiving services in primary care settings and from participating in clinical studies. Homebound issues may be particularly important for African American CGs, yet the minority CG literature has not addressed relevant issues for homebound dyads. Nor are the chronic needs of homebound dementia care dyads adequately attended by the current home health care system, which now focuses on skilled nursing care. This study has been designed to address these research deficits. The study will examine the benefit (through improving depression, anxiety, and health perception) and the cost-effectiveness of home-based dementia caregiving interventions, with attention to both the informal care provided by the CG and the use of formal care services. Care dyads will be randomized to either Usual Care or Enhanced Care. Both Usual Care and Enhanced Care caregivers will receive usual home health care delivered by home health nurses on the schedule determined by the patient's needs and set by the home care agency. For the Enhanced Care caregivers, to ensure protocol adherence, using the same schedule as the home health visits, trained interventionists from the research staff will deliver the intervention. The interventionists will teach dementia family caregivers to cope with difficult care recipient behaviors and challenges to caregiving and will teach caregivers how to cope with their own responses to caregiving. Following established protocols and using fifth grade level pamphlets and educational material, the interventionists will tailor the intervention sessions to meet the individual needs of each care dyad in their own home environment. Enhanced Care sessions will not exceed 60 minutes. Research specialists will perform data collection visits in the care dyads’ homes at baseline, within 2 weeks of home care ending and six months.


Criteria:

Inclusion Criteria: 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 Criteria: 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.


NCT ID:

NCT00182897


Primary Contact:

Principal Investigator
Linda Nichols, PhD
Program Director, Interprofessional Team Training & Development, Veterans Affairs Medical Center


Backup Contact:

N/A


Location Contact:

Memphis, Tennessee 38163
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.