Dementia - Subcortical |
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Clinical Trial: Telephone-Based Support for Caregivers of Patients with Dementia
This study is no longer recruiting patients.
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Purpose
The purpose of this study is to develop an effective, low-cost, telephone-based intervention to reduce anxiety, depression, and feelings of burden and stress in caregivers of patients with dementia. This study will also determine whether the intervention can alter the course of dementia.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Dementia | Behavior: Cognitive-Behavioral Family Systems Intervention | Phase II Phase III |
MedlinePlus related topics: Dementia
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: A Telephone Intervention for Dementia Caregivers
Expected Total Enrollment: 85
Study start: December 2001; Study completion: November 2005
Caregivers are randomized to receive either telephone-based intervention or standard medical care. Both groups receive a resource packet containing information about caring for someone with dementia and a list of local resources. Caregivers in the intervention group also receive a series of telephone calls over 12 months, during which education, emotional support, and training in problem-solving skills are provided by trained therapists. Caregivers in the standard care group receive no additional psychosocial intervention. Participants are assessed pre-treatment, mid-treatment (6 months), post-treatment, and at a 3-month follow-up.
Eligibility
Ages Eligible for Study: 18 Years - 90 Years, Genders Eligible for Study: Both
Accepts Healthy Volunteers
Criteria
Patient Inclusion Criteria:
- DSM-IV diagnosis of dementia (vascular, mixed, or associated with Alzheimer’s disease)
- Lives in the community, including senior/retirement centers, but excluding nursing homes and assisted living centers
- 50 years old or older
- Resides in Southeastern New England
Caregiver Inclusion Criteria:
- Living with a person with dementia
- Provides care for at least 6 months for at least 4 hours a day
- English as primary language
- Telephone access
- Resides in Southeastern New England
Patient Exclusion Criteria:
- Major acute medical condition affecting independent functioning
Caregiver Exclusion Criteria:
- Acute medical illness
- Cognitive impairment as defined by an MMSE score < 25
Location Information
Rhode Island
Rhode Island Hospital, Providence, Rhode Island, 02903, United States
More Information
Record last reviewed: November 2004
Last Updated: November 29, 2004
Record first received: January 22, 2003
ClinicalTrials.gov Identifier: NCT00052104
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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