Automated cognitive screening tool for primary care providers
Cognitive Screening Made Easy for PCPs - R33 Phase
This study is testing a new automated tool to help doctors easily spot early signs of cognitive decline in older adults so they can get the care they need sooner.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 500 (estimated) |
| Ages | 60 Years and up |
| Sex | All |
| Sponsor | University of Texas at Austin Academic / other |
| Locations | 1 site (Austin, Texas) |
| Trial ID | NCT06162026 on ClinicalTrials.gov |
What this trial studies
This project aims to enhance early detection of cognitive decline in older adults by developing an automated risk assessment and cognitive screening tool specifically for primary care providers. The tool is designed to streamline the screening process, making it easier for providers to identify patients who may need further evaluation or treatment. By addressing the needs of primary care providers, the project seeks to increase the number of older adults screened for cognitive impairment, thereby improving early intervention opportunities. The long-term goal is to create a user-friendly tool that is sensitive to cognitive decline across diverse populations.
Who should consider this trial
Good fit: Ideal candidates for this study are older adults aged 60 years and older who are fluent in English and come from diverse ethnic and racial backgrounds.
Not a fit: Patients with prior diagnoses of dementia or significant cognitive impairment that affects their ability to follow instructions will not benefit from this study.
Why it matters
Potential benefit: If successful, this tool could lead to earlier identification and treatment of cognitive decline in older adults, potentially improving patient outcomes.
How similar studies have performed: Other studies have shown success with similar automated screening approaches, indicating potential for this tool to be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Aged 60 years and older; * Ethnic/racial background consistent with NIH policy * Male or female * Fluent in English. Exclusion Criteria: * Confounding conditions that could impact ability to participate in the study (e.g., cognitive impairment sufficient to impact ability to follow instructions on the iPad, motor impairment that would prohibit independent use of RACS, poor visual acuity) * Prior diagnosis of dementia * Non-English speaking.
Where this trial is running
Austin, Texas
- Family Wellness Clinic — Austin, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Robin C Hilsabeck, PhD — University of Texas Health Sciences Center at San Antonio
- Study coordinator: Robin C Hilsabeck, PhD
- Email: hilsabeck@uthscsa.edu
- Phone: 210-835-8748
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.