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Testing the Effectiveness of Telephone Support for Dementia Caregivers (CONNECT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00119561
Recruitment Status : Completed
First Posted : July 13, 2005
Last Update Posted : April 7, 2015
Information provided by (Responsible Party):
VA Office of Research and Development ( US Department of Veterans Affairs )

Brief Summary:
The primary goal of the study is documentation of effectiveness of telephone support groups to reduce caregiver burden and stress. Caregivers who participate in intervention (Telephone Support) should experience lower levels of stress, burden and health care utilization (lower use of psychotropic drugs, fewer scheduled/unscheduled medical visits, lower rates of institutionalization, more efficient use of time in managing care recipient problems) compared to those caregivers in Usual Care.

Condition or disease Intervention/treatment Phase
Dementia Alzheimer Disease Behavioral: Telephone Support Not Applicable

Detailed Description:

Background: Caregiving can severely limit caregivers' lives. In order to keep their family member at home, dementia caregivers often experience physical and psychological strain, social isolation, loss of time for self, and inability to obtain and/or afford assistance with caregiving tasks. The amount of time spent in providing care for a family member with dementia contributes to these problems. Dementia caregivers report spending around 18 hours per day in caregiving tasks and 3 hours per day in supervision. The high levels of stress involved in caring for a dementia patient and the widespread lack of training in such care can lead to a vicious cycle of ever-increasing health care dependency, first for the patient and secondly for informal caregivers. Telephone Support Groups have the potential to address caregivers' stress, isolation and education about dementia and its management, leading to sustainable informal caregiving and lower healthcare use and overall VHA expenditures for the veteran patient with dementia.

Objectives: Study objectives are to 1) examine Telephone Support Groups' effectiveness for caregivers, 2) determine whether Telephone Support results in decreases in VHA health care use and costs for the veteran, and decreased VHA and/or non-VHA use and costs for the caregiver, and 3) examine the intervention's effect on caregivers' time spent providing care. The long-term objective is to develop and disseminate the protocol and materials for effective Telephone Support Groups that can be used across the VHA system.

Methods: This randomized clinical trial of 154 caregivers (Black/African American, White/Caucasian, rural, urban) compared dementia caregivers participating in Telephone Support Groups to caregivers whose family members with dementia were receiving usual care. Either the caregiver or the patient had to be a veteran receiving care at the VAMC Memphis. In the treatment condition, there were 15 year-long support groups of one trained group leader and 5 to 6 caregivers. Each support group met 14 times. The one hour calls were semi-structured conference calls with education, coping skills and cognitive restructuring, and support components. A Caregiver Notebook with information on each topic provided materials for the educational sessions. Topics included knowledge of dementia, safety, caregiver health and well being, communication, managing behavioral challenges, and caregiver stress and coping. A workshop focusing on the same behavior management and stress topics was offered to Usual Care caregivers at the end of their participation.

Data were collected in caregivers' homes by trained Research Associates at baseline, six and twelve months. VHA health care use and data for the veteran were based on the Patient Treatment File (PTF) and the Outpatient Clinic File (OPC) and costs data used the Health Economics Resource Center (HERC) Average Cost Data Sets.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 154 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Testing the Effectiveness of Telephone Support for Dementia Caregivers
Study Start Date : February 2005
Actual Primary Completion Date : June 2007
Actual Study Completion Date : January 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Caregivers Dementia

Arm Intervention/treatment
Experimental: Arm 1
Telephone support groups
Behavioral: Telephone Support
Each telephone support group of 5 caregivers and a group leader met 14 times over a year. The hour calls were semi-structured with an educational component and a support component, led by a trained Group Leader. Topics included knowledge of dementia, safety, caregiver health and well being, communication, managing behavioral challenges and caregiver stress and coping.

No Intervention: Arm 2
Usual VA care

Primary Outcome Measures :
  1. General well-being (revised Rand General Well-Being Scale); and caregiver's level of distress with care recipient behaviors (Revised Memory and Behavior Problems Checklist). Data is collected at baseline, 6 and 12 months in a face to face interview. [ Time Frame: 6 and 12 months ]

Secondary Outcome Measures :
  1. Cost-Effectiveness [ Time Frame: 6 and 12 months ]
  2. Time spent providing care [ Time Frame: 6 and 12 months ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   21 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:


  • Age: 21 years or older
  • Family member of the care recipient
  • Must live with care recipient or share cooking facilities
  • Must have a telephone
  • Must plan to remain in the area for the duration of the intervention and follow-up
  • Caregiver role for more than 6 months
  • Must provide an average of 4 hours of supervision or direct assistance per day for the care recipient
  • Risk Screening Tool: must have a total score of at least 1 for question 36, and a total of at least 2 for questions 38-40 (on the Screening Form)

Care Recipient

  • NINCDS (MD diagnosis) or cognitive impairment (raw score on MMSE of 23 or less)
  • Must be a Veteran with dementia or being cared for by a Veteran who receives services at the Memphis VAMC

Exclusion Criteria:


  • Active treatment (chemotherapy; radiation therapy) for cancer
  • Imminent placement of care recipient into a nursing home (within 6 months)
  • SPMSQ: > 4 errors

Care Recipient

  • History of Parkinson's Disease or a stroke with no reported decline in memory over the past year
  • 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 (onset of delusions before age 45) or other severe mental illness
  • Dementia secondary to head trauma (probable)
  • Blindness or deafness if either disability prohibits them from data collection or participation in the interventions
  • MMSE = 0 and Bedbound (routinely confined to bed or chair for at least 22 hours a day, for at least 4 of the last 7 days)
  • Planned nursing home admission in 6 months

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00119561

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United States, Tennessee
Memphis VA Medical Center, Memphis, TN
Memphis, Tennessee, United States, 38104
Sponsors and Collaborators
US Department of Veterans Affairs
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Principal Investigator: Linda Olivia Nichols, PhD Memphis VA Medical Center, Memphis, TN
Publications of Results:
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Responsible Party: US Department of Veterans Affairs Identifier: NCT00119561    
Other Study ID Numbers: IIR 03-287
First Posted: July 13, 2005    Key Record Dates
Last Update Posted: April 7, 2015
Last Verified: July 2014
Keywords provided by VA Office of Research and Development ( US Department of Veterans Affairs ):
Alzheimer Disease
Randomized Controlled Trials
Additional relevant MeSH terms:
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Alzheimer Disease
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurodegenerative Diseases
Neurocognitive Disorders
Mental Disorders