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NCT05159583Completed

In-Home Technology for Caregivers of People With Dementia and Mild Cognitive Impairment: Rural Homes

Commercializing In-Home Supportive Technology for Dementia Caregivers

Source: ClinicalTrials.gov · Last updated 25 Feb 2025

Brief summary (registry, in English)

This study aims to develop, evaluate, and commercialize an in-home supportive technology that is designed to alleviate anxiety, burden, and loneliness in spousal and familial caregivers of individuals with Alzheimer's disease, other dementias, or mild cognitive impairment in rural homes.

Status (registry)
Completed
Study type
Interventional
Enrollment
15 (actual)
First submitted
2 Dec 2021
Start date
22 Aug 2022
Primary completion date
30 Jan 2024
Lead sponsor
University of California, Berkeley
NCT number
NCT05159583

What you commit to

  • Study type: Interventional
  • Participants enrolled: 15
  • From 22 Aug 2022 to the primary completion date, 30 Jan 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.

Prior treatment

  • Caregivers providing care for individuals who use a medication likely to affect central nervous system functions adversely

Other illness

  • Caregivers providing care for individuals with known non-neurodegenerative conditions affecting behavior and cognition
  • Caregivers providing care for individuals with longstanding Axis I psychiatric disorder
  • Caregivers providing care for individuals with metabolic disorder or major organ dysfunction
  • Caregivers providing care for individuals with alcohol abuse or dependence (within 5 years of dementia onset)
  • Caregivers providing care for individuals with significant systemic medical illness

Other

  • Caregivers providing care for individuals with head trauma with loss of consciousness greater than 30 minutes
  • Caregivers providing care for individuals with contraindications to MRI imaging
  • Caregivers providing care for individuals with large confluent white matter lesions

Who the study is looking for

  • Caregivers are fluent/literate in English
  • Caregivers currently reside in the United States with spouse/family member who has received a medical diagnosis of Alzheimer's disease, other dementia, or mild cognitive impairment
  • Caregivers live in rural areas (using Rural-Urban Commuting Area Codes data)
  • Caregivers primarily use a smartphone (e.g., iPhone, Android)

Age in the registry: 18 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
University of California, Berkeley
Coordinator of this site? Confirm its status
BerkeleyUnited StatesUnknown status

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