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NCT05012410Completed

WeCareAdvisor Study for Caregivers of People Living With Dementia

Efficacy of the WeCareAdvisor: An Online Tool to Help Caregivers Manage Behavioral and Psychological Symptoms in Persons Living With Dementia

Source: ClinicalTrials.gov · Last updated 30 Sept 2025

Brief summary (registry, in English)

The WeCareAdvisor is an online tool to help caregivers manage behavioral and psychological symptoms of people living with dementia. The trial will evaluate its efficacy to reduce caregiver distress, improve confidence managing behaviors, as well as reduce occurrences and severity of behavioral and psychological symptoms. Visit https://wecareadvisorstudy.com/ for more information.

Status (registry)
Completed
Study type
Interventional
Enrollment
262 (actual)
First submitted
6 Aug 2021
Start date
13 Dec 2021
Primary completion date
19 Jul 2024
Lead sponsor
Drexel University
NCT number
NCT05012410

What you commit to

  • Study type: Interventional
  • Participants enrolled: 262
  • From 13 Dec 2021 to the primary completion date, 19 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Caregiver currently involved in another clinical trial of psychosocial or educational interventions for dementia;
  • Caregiver has a visual impairment that prohibits interaction with the tool, and/or have a hearing impairment sufficient to prohibit telephone communication;
  • Caregiver reports person living with dementia is not responsive to his/her environment (e.g., unable to understand short commands or recognize a person coming in/out of the room);
  • Caregiver reports person living with dementia is an active suicide risk
  • Caregiver reports person living with dementia is likely to have an imminent placement in a long-term care facility (within 6 months).
  • Either caregiver/person living with dementia has a terminal disease with life expectancy \< 6 months, is in active treatment for cancer, or has had more than 3 acute medical hospitalizations over the past year.

Who the study is looking for

  • self-identify as the primary caregiver to the person living with memory loss or dementia;
  • has been a primary caregiver for at least 6 months;
  • report managing \>1 behavioral symptom(s) in the past month;
  • has an email account or smartphone (to receive daily tips and reminder messages);
  • English speaking;
  • has own smartphone, tablet, laptop, or desktop computer and access to Internet;
  • If person living with dementia is on an anti-dementia or psychotropic medication, they must be on a stable dose for at least 60 days prior to enrollment.
  • If caregiver is on an anti-depression or other psychotropic medication, they must be on a stable does for at least 60 days prior to enrollment
  • Lives in the United States or US territory

Age in the registry: 21 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Drexel University
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.