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Telephone Support for Dementia Caregivers

Psychosocial Telephone Intervention for Dementia Caregivers

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00735800
Enrollment
250
Registered
2008-08-15
Start date
2008-02-29
Completion date
2013-05-31
Last updated
2015-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Keywords

Dementia, Caregivers, Alzheimer's disease

Brief summary

Caring for a patient with dementia is associated with increased feelings of burden and depression. The proposed study will examine the efficacy of Family Intervention: Telephone Tracking - Dementia (FITT-Dementia), a multi-component, family-based, telephone intervention, as a tool to reduce caregiver stress.

Detailed description

A previous pilot study of this approach showed reduced burden and reaction to memory and behavior problems for dementia caregivers. This study will test the intervention in a larger group of caregivers and have a more detailed analysis of outcomes. The caregiver of a person with dementia will receive telephone support calls. They will receive telephone calls from a trained member of the research team. These calls will occur over a six-month period and will be scheduled at a time that is convenient for the caregiver. They will receive a total of 16 calls over 6 months. During each call, the support person will discuss their current caregiving situation and provide various forms of support.

Interventions

BEHAVIORALFamily Intervention:Telephone Tracking Support- Caregiver

Family-based problem solving treatment

Supportive telephone counseling about caregiving

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Rhode Island Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* 1\) Diagnosis of dementia; * 2\) mild to moderate dementia; * 3\) family member or other adult in caregiver role for at least 6 months, and who provides at least 4 hours of supervision or direct assistance per day for the person with dementia; * 4\) care recipient lives in the community, including senior/retirement centers, but excluding nursing homes and assisted living centers; and * 5\) there is no plan for the care recipient to be placed in long term care or the caregiver to end their role within the next 6 months

Exclusion criteria

Patient: * 1\) other major medical condition affecting independent functioning * 2\) older than age 90; and * 3\) younger than age 50. Caregiver: * 1\) major acute medical illness; * 2\) English not primary language; * 3\) cognitive impairment; * 4\) no access to a telephone; or * 5\) older than age 90.

Design outcomes

Primary

MeasureTime frame
Depression, burden, reaction to memory and behavior problemsEvery two months, over a 6 month time-period , and a three month follow-up

Secondary

MeasureTime frame
Cost-effectiveness and resource useMonthly resource check-ins.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026