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Telephone-Based Support for Caregivers of Patients with Dementia - Article


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Dementia

Senility




Clinical Trial: Telephone-Based Support for Caregivers of Patients with Dementia

This study is no longer recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

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

Further Study Details: 

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

Study ID Numbers:  62561-01A1
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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Page Updated: May 11, 2006
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