Mode
Text Size
Log in / Sign up
N/A Completed N=22 Randomized Supportive Care

Socially Assistive Robots for Interaction With Older Adults With Dementia

Source: ClinicalTrials.gov NCT04384978 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcomePrimary: Change in Cognitive/Memory Ability — 23.75 score on a scale

Summary

A 12-month pilot study will be comprised of two groups of people diagnosed with mild Alzheimer's disease and related dementia for a total of 80 senior subjects. Subjects will be randomly assigned to two groups: Group 1 users will play games with and administered by Ryan, 2-3 times a week and 30-minutes per day. Group 2 (Active Control Group) will play solitary games and activities but will have to interaction with Ryan. The team will measure the changes and improvement in the social/emotional well-being of these two groups and eventual changes in the cognitive/memory functions of elderly people living in the similar environment.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Cognitive/Memory Ability
23.75

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 65 years
  • Early Alzheimer's disease and related dementia diagnosed by a qualified provider
  • Saint Louis University Mental Status (SLUMS) score between 10 and 25
  • Resident of assisted living facility for at least one month prior and for the duration of the study
  • Deemed conditioned enough to participate in physical activities after a wellness check
  • Verbal skill to interact
  • Participant or Legal decision

Exclusion Criteria

Aggressive behavior

  • Diagnosed with severe dementia or memory loss
  • Acute physical illness that impairs ability to participate
  • Patients with serious comorbidity, tumors and other diseases casually related to cognitive impairment
  • History of alcohol or drug abuse, head trauma, psychoactive substance use and other causes of memory impairment
  • Significant sensory impairment
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04384978). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search