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N/A N=244 Randomized Double-blind Supportive Care

Caring for the Caregiver Network

Caregivers of Alzheimer's Disease or Memory Problem Patients

Enrolled (actual)
244
Serious AEs
Results posted
Jun 2019
Primary outcome: Primary: Depression as Measured by Center for Epidemiologic Studies Depression Scale (CES-D) — 11.38; 10.88; 10.86; 10.69 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Caregiving condition (Behavioral); Nutrition condition (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Miami
Primary completion
Apr 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Depression as Measured by Center for Epidemiologic Studies Depression Scale (CES-D)
11.38; 10.88; 10.86; 10.69; 10.32; 10.46
PRIMARY
Caregiving Burden as Measured by Burden Inventory
18.52; 19.66; 16.89; 18.23; 16.08; 17.66
PRIMARY
Caregiver's Self Report of Self-care
0.62; 0.60; 0.62; 0.60; 0.62; 0.61
PRIMARY
Caregiver's Self-report of Physical Health
2.71; 2.75; 2.89; 2.51; 2.76; 2.67
PRIMARY
Caregiver's Self-efficacy
925.21; 936.65; 971.43; 964.15; 999.65; 1047.71
PRIMARY
Positive Aspects of Caregiving
24.46; 23.24; 24.72; 24.02; 24.00; 24.58

Summary

The prevalence of family caregivers is projected to increase in concert with the projected increase in number of AD patients. The focus of the study is to gather systematic data on the acceptability and efficacy of a unique technology-based, culturally- tailored psycho-social intervention program that targets ethnically/culturally diverse family caregivers of patients with Alzheimer's Disease. The overall goal of the project is to improve the lives of family caregivers as well as their ability to provide care to their loved one and to reduce disparities in access to needed services and support among caregiver populations.

Eligibility Criteria

Inclusion Criteria

  • Speak and understand English or Spanish
  • Provide care to a loved one with memory decline
  • Not having terminal illness/condition
  • 18+ yrs old

Exclusion Criteria

  • Not providing care to a loved one with Alzheimer disease or dementia
  • Not speak English or Spanish
  • Have cognitive deficit
  • Have terminal illness
  • Plan to place their loved one in a facility
  • Plan to move away in the next 12 months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03049501). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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