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N/A Completed N=32 Randomized Single-blind Supportive Care

VA Cultivating Access to Resources, Education, and Skills for Dementia Caregivers

Dementia · Caregivers · Neurodegenerative diseases · Brain Diseases
Source: ClinicalTrials.gov NCT02106065 ↗
Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Aug 2021
Primary outcomePrimary: Zarit Burden Inventory — 2.0; -0.4; 1.6 score on a scale

Summary

The purpose of this study is to study the effects of an education and skill-building intervention on family caregivers of Veterans with dementia.

Outcome Measures

OutcomeResultp-value
PRIMARY
Zarit Burden Inventory
2.0; -0.4; 1.6
SECONDARY
Center for Epidemiological Studies-Depression
2.0; 0.1; -0.2
SECONDARY
Long-term Care Placement Status (Care Recipient)
SECONDARY
Change in All-cause Mortality Status (Care Recipient)
1; 0; 1

Eligibility Criteria

Inclusion Criteria

Inclusion criteria -- Participants must:

  • be adults (age 18)
  • report distress associated with being the primary caregiver for a Veteran family member with all-cause dementia
  • reporting at least 2 of the following 6 items at baseline assessment: felt overwhelmed, felt like they often needed to cry, were angry or frustrated, felt they were cut off from family or friends, reported moderate to high levels of general stress, or felt their health had declined
  • provide at least one hour of care (supervision or direct assistance) per week over the past 3 months (other sources of caregiving for the Veteran with dementia can also be utilized; e.g., respite, home health aide, other family members, etc.)
  • be proficient in spoken and written English
  • be capable of providing informed consent

Exclusion Criteria

Exclusion criteria -- Potential participants will be screened and excluded for:

  • current or lifetime history of any psychiatric disorder with psychotic features
  • prominent suicidal or homicidal ideation
  • having met DSM-IV criteria for drug or alcohol abuse or dependence (except nicotine) within the past six months
  • presence of alcohol intoxication (by breathalyzer) or alcohol withdrawal (by exam) during study recruitment or participation
  • diagnosis of probable or possible dementia
  • a Telephone Cognitive Screen score of < 20
  • participation in another caregiver intervention within the past year
  • lack of regular access to a telephone
  • illness that would prevent 24 months of study participation
  • planned transfer of care receiver to another caregiver or nursing home within 12 months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02106065). 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. Informational only — not medical advice.

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