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WeCareAdvisor: A Web-Based Tool to Improve Quality of Life for Military Veterans With Dementia and Their Caregivers

WeCareAdvisor: A Web-Based Tool to Improve Quality of Life for Military Veterans With Dementia and Their Caregivers

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04587583
Enrollment
19
Registered
2020-10-14
Start date
2020-10-19
Completion date
2021-10-21
Last updated
2022-03-31

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

Conditions

Alzheimer Disease, Behavioral Symptoms, Caregiver, Dementia, Memory Disorders

Brief summary

This research will test the WeCareAdvisor tool for family caregivers of military veterans with dementia to help caregivers assess, manage and track behavioral symptoms and their contributing factors (e.g., pain, sleep disturbance), and that provides tailored strategies for in-home, medication-free behavior management. 60 caregiver-person with dementia dyads will be recruited (30 Treatment Group, 30 Wait-List Control Group).

Interventions

BEHAVIORALWeCareAdvisor

Tailored, internet-based software intended to assess, manage and track behavioral symptoms and their contributing factors and to instruct dementia caregivers in problem solving approaches (tailored strategies for in-home, medication-free behavior management) to address difficult or disruptive behaviors exhibited by the person with dementia. During the testing period participants will refer to the WeCareAdvisor when behavioral challenges occur.

Sponsors

United States Department of Defense
CollaboratorFED
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Eligible caregivers must: * Be the primary caregiver of a military veteran with dementia for at least 6 months and planning to remain the primary caregiver for the next 2 months * Currently living with the person they are caring for (care recipient) * Comfortable utilizing technology (e.g. computers, tablets, the internet) * Have access to the internet and a computer or tablet device * Plans to live in the area for the duration of the study Care recipients (military veteran living with dementia) must: * Exhibit at least one or more behavioral symptoms (any behavior at any frequency) * Receiving psychotropic medication or cognitive enhancers will not exclude the care recipient. * Have a clinical diagnosis of dementia (any type) per caregiver report. * Be a military veteran.

Exclusion criteria

* Inability to read, speak or understand English * Lack of regular access to a telephone, internet, technology (tablet or computer) * Caregiver is unable to use a computer or tablet * Person with dementia is not a military veteran

Design outcomes

Primary

MeasureTime frameDescription
Change in Caregiver StressBaseline to 2 monthsAs measured by a study specific questionnaire completed by caregivers. Stress is measured on a scale of 1 to 5 where 1 is equivalent to no stress and 5 is equivalent to extreme stress.
Change in Caregiver Confidence in Managing Problematic BehaviorBaseline to 2 monthsAs measured by a study specific questionnaire completed by caregivers. Confidence in managing problematic behavior is measured on a scale of 0 to 10, where a score of 0 means not confident and 10 means extremely confident
Change in Caregiver UpsetBaseline to 2 monthsAs measured by a study specific questionnaire completed by caregivers. Upset is measured on a scale of 0 to 5 where 0 is equivalent to no upset and 5 is equivalent to extreme upset (midpoint is equivalent to fairly upset).

Secondary

MeasureTime frameDescription
Change in Caregiver CommunicationBaseline to 2 monthsCaregivers rate the frequency of using six forms of negative communication (yelling, threatening, criticizing, withdrawing from patient, using harsh tone and screaming), measured on a scale of 1 to 5 where a score of 1 is never and a score of 5 is always.

Other

MeasureTime frameDescription
Ease of Use of the WeCareAdvisor Tool1 month after using WeCareAdvisor toolAs measured by a study specific questionnaire completed by caregivers. Ease of use of the WeCareAdvisor tool is measured on a scale of 1 to 7 where 1 is equivalent to strongly disagree and 7 is equivalent to strongly agree (midpoint is equivalent to neutral).
Usefulness/ Perceived Benefit of the WeCareAdvisor Tool1 month after using WeCareAdvisor toolAs measured by a study specific questionnaire completed by caregivers. Usefulness/perceived benefit of the WeCareAdvisor tool is measured on a scale of 1 to 7 where 1 is equivalent to strongly disagree and 7 is equivalent to strongly agree (midpoint is equivalent to neutral).

Countries

United States

Outcome results

None listed

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