50 Participants NeededMy employer runs this trial

HiDO HomeCareSystem for Dementia

CG
Overseen ByCharles Gellman
Age: 65+
Sex: Any
Trial Phase: Academic
Sponsor: HiDO Technologies
Must be taking: Dementia medications
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether a new tool, the HiDO HomeCareSystem, can help people with dementia take their daily medications more reliably. The system uses face recognition to remind users when to take their meds, aiming to improve overall health outcomes. Participants must have dementia, be on medication for it, and have a caregiver to assist with the study. The trial compares the HiDO system to normal medication routines to determine its effectiveness.

As an unphased trial, this study offers patients the chance to contribute to innovative solutions that could enhance daily living for those with dementia.

Will I have to stop taking my current medications?

You might need to stop taking certain medications if they are contraindicated (not safe to use together) with the study. The research team will review your medications and work with your doctor to decide if any changes are needed before you join the trial.

What prior data suggests that the HiDO HomeCareSystem is safe for use in dementia patients?

Previous studies have tested the HiDO HomeCare System for safety and effectiveness in medication management. Research shows that this device uses face recognition to remind patients to take their pills. It assists people with dementia in taking medication correctly, reducing the chances of missed doses or incorrect medication.

The studies primarily focused on the device's effectiveness rather than side effects. The trial is labeled "Not Applicable," indicating insufficient data from early human trials for detailed safety information. However, devices like this are generally considered low-risk and undergo testing to ensure safe use as intended.

Available studies report no serious side effects from the HiDO HomeCare System. Overall, the device appears well-tolerated by patients and offers an innovative way to help people with dementia manage their medication safely at home.12345

Why are researchers excited about this trial?

The HiDO HomeCare System is unique because it uses face recognition technology to assist individuals with dementia in managing their medication. Unlike traditional methods where patients or caregivers must remember dosing schedules, this system helps monitor and ensure timely medication intake, potentially reducing the chance of missed or incorrect doses. Researchers are excited about this system because it empowers both patients and their caregivers, offering a more personalized and reliable way to manage medication, which may improve overall treatment outcomes and quality of life for those living with dementia.

What evidence suggests that the HiDO HomeCareSystem is effective for improving medication compliance in dementia?

Research has shown that the HiDO HomeCareSystem, which participants in this trial may use, holds promise for helping people with dementia take their medication as prescribed. Studies indicate that this device overcomes the shortcomings of older medication management tools. It supports correct medication adherence, which is essential for managing dementia effectively. Additionally, the system is linked to better overall care for dementia, offering support to both patients and their caregivers. Early findings suggest the device helps caregivers by reducing stress and improving their ability to manage care. Participants in the trial will be randomized to either use the HiDO HomeCareSystem or continue with Standard Medication Management without the device.12346

Are You a Good Fit for This Trial?

This trial is for people diagnosed with dementia who take at least two daily medications (one for dementia symptoms) and have a study partner willing to help monitor their medication use. Participants must allow home visits for device installation and meet certain cognitive test scores.

Inclusion Criteria

Participants must have an active study partner willing to be enrolled, receive messages and alerts from the HiDO-ALZ system if medications are missed, and complete surveys about the participant's ongoing health
Participants must be willing to allow research staff to enter their homes to install the HiDO-ALZ device and complete study activities
I am taking a dementia medication and at least one other medication.
See 3 more

Exclusion Criteria

Participants with MoCA scores below 15
I am unable to understand or agree to participate in this study.
I am able and willing to complete cognitive and blood tests.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants use the HiDO-ALZ device to improve medication compliance and health outcomes

12 months
Monthly check-ins (virtual or in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • HiDO HomeCareSystem

Trial Overview

The study is testing the HiDO-ALZ HomeCareSystem, a device designed to help people with dementia remember to take their medications by sending reminders and alerts to both participants and their caregivers.

How Is the Trial Designed?

2

Treatment groups

Active Control

Group I: HiDO HomeCare SystemActive Control1 Intervention
Group II: Standard Medication ManagementActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

HiDO Technologies

Lead Sponsor

Trials
2
Recruited
80+

University of California, Davis

Collaborator

Trials
958
Recruited
4,816,000+

National Institute on Aging (NIA)

Collaborator

Trials
1,841
Recruited
28,150,000+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/41921136/

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