Fact CheckerSign in

NCT05527405Completed

Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes

Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes in Visual Mapping Assistive Technology

Source: ClinicalTrials.gov · Last updated 10 Jun 2026

Brief summary (registry, in English)

As part of Phase II of the NIH SBIR grant, the study will conduct a randomized controlled clinical trial in which the MapHabit system (MHS) will offer a caregiver training product in adjunct. MHS is an Alzheimer's disease or related dementias (ADRD) assistive technology product that uses visual maps to improve the quality of life of persons living with dementia (PLWD) and reduce the burden of care partners. The study will primarily investigate the efficacy of the Caregiver Training Program (CTP), a personalized dementia caregiver education service that is integrated into the MHS product. The study will be a randomized controlled clinical trial, in which two conditions will be investigated: 1) control condition in which the MHS alone is incorporated in the caregiver's daily care for PLWD and 2) experimental condition in which the MHS+CTP is implemented into the caregiver's daily care for PLWD. The sample size will be a total of 50 caregiver-PLWD dyads, 25 in each condition. This means the primary participant will be the caregiver, while the PLWD under the caregiver's care is considered the co-participant. Hence, 50 participant dyads enrolled will equate to 100 participants enrolled total. The study will be a 6-month intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
31 Aug 2022
Start date
24 Aug 2024
Primary completion date
15 Dec 2025
Lead sponsor
MapHabit, Inc.
NCT number
NCT05527405

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 24 Aug 2024 to the primary completion date, 15 Dec 2025
  • 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

  • Participating caregiver of individual with dementia is NOT the primary caregiver

Other

  • Care/support recipient not diagnosed with ADRD
  • Not proficient in English

Who the study is looking for

  • Participating caregiver of individual with dementia must be the primary caregiver
  • Care recipient must be an individual diagnosed with Alzheimer's disease or other related dementia (ADRD) in their mild to moderate stage of impairment
  • Proficient in English

Age in the registry: 18 years to - · Sex: All · Does not accept 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
MapHabit, Inc.
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status

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