CompletedNot Applicable

SimpleC Wellness Platform With Social Robot Interaction

United States26 participantsStarted 2022-02-03

Plain-language summary

This implementation study will be conducted to test a Socially-Assistive Robot (SAR) system for residents in an Assisted Living environment. The goal of the SAR system is to enhance social engagement and connectedness. The system engages residents via robot-facilitated activities such as trivia and reminder and is integrated with the SimpleC Wellness Platform.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * All: Fluent in English * Resident: 50 years and older * Resident: lives in Assisted Living Community * Resident: MMSE score of 13 or higher * Family member: 18 years and older * Family member: family or friend of resident * Family member: no diagnosis of dementia or related disorder * Staff: 18 years and older * Staff: works for the Senior Housing Community Exclusion Criteria: * All: pregnant * Resident: Expecting to move during the study * Resident: Both legally deaf and blind

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Facilitators to Successful Implementation

Timeframe: 3 weeks

Barriers to Successful Implementation

Timeframe: 3 weeks

Trial details

NCT IDNCT05296239

SponsorSimpleC, LLC

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2022-03-07

Results submitted2025-08-07

View on ClinicalTrials.gov More Engagement, Patient trials