Using robots to help older adults with cognitive impairment and apathy
Impact of a Novel Socially Assistive Robotic Architecture on Engaging Older Adults With Mild Cognitive Impairment, Alzheimer's Disease and Related Dementia in Long Term Care Settings
PHASE1; PHASE2 · Vanderbilt University · NCT05178992
This study is testing whether using a robot can help older adults with cognitive impairment feel less apathetic and more engaged in activities while living in long-term care facilities.
Quick facts
| Phase | PHASE1; PHASE2 |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Vanderbilt University (other) |
| Locations | 1 site (Nashville, Tennessee) |
| Trial ID | NCT05178992 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of a socially assistive robot system in reducing apathy among older adults with cognitive impairment living in long-term care facilities. Participants will be randomly assigned to either standard activity programs or those enhanced with robotic activities. The study will also explore individual and facility factors that may influence the effectiveness of the robotic interventions. Previous phases have shown the feasibility and acceptability of using such robotic systems in this context.
Who should consider this trial
Good fit: Ideal candidates are older adults residing in long-term care facilities with mild to moderate cognitive impairment and symptoms of apathy.
Not a fit: Patients with severe cognitive impairment or those who are physically unable to participate will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the quality of life for older adults with cognitive impairment by reducing apathy.
How similar studies have performed: Previous studies have shown promise in using robotic systems for social interaction in similar populations, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Residing \>3 months in long term care facility * Evidence of mild cognitive impairment (SAGE score 15-16), mild dementia (SAGE score \<15, AD8\<2, DSRD\<19), or moderate dementia (SAGE \<15, AD8\>1, DSRD 19-36) * Symptoms of apathy (Score 30+ on AES-C) Exclusion Criteria: * Severe cognitive impairment * Physically unable to participate * Unable to provide assent * Uncorrected vision or hearing * Never spoke English * Unable to sit comfortably in chair * Acutely ill, terminally ill or unresponsive * Unable to be moved to activity location * Aggressive or combative
Where this trial is running
Nashville, Tennessee
- Vanderbilt University — Nashville, Tennessee, United States (RECRUITING)
Study contacts
- Study coordinator: Kelley Colopietro, BS
- Email: kelley.j.colopietro@vanderbilt.edu
- Phone: 4436176792
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Alzheimer Disease, Apathy, Robotics, Virtual Reality