ACTIVE_NOT_RECRUITING

Cognitive Screening Made Easy for PCPs - R33 Phase

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This project will facilitate early detection of cognitive decline in older adults through development and implementation of an automated risk assessment and cognitive screening tool for use in primary care. By providing an automated tool developed specifically to address the needs of PCPs, it will be easier to screen for cognitive impairment, increasing the number of older adults who are screened and thus identified and treated.

Official Title

Cognitive Screening Made Easy for PCPs - R33 Phase

Quick Facts

Study Start:2024-02-02
Study Completion:2027-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06162026

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged 60 years and older;
  2. * Ethnic/racial background consistent with NIH policy
  3. * Male or female
  4. * Fluent in English.
  1. * 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)
  2. * Prior diagnosis of dementia
  3. * Non-English speaking.

Contacts and Locations

Principal Investigator

Robin C Hilsabeck, PhD
PRINCIPAL_INVESTIGATOR
University of Texas Health Sciences Center at San Antonio

Study Locations (Sites)

Family Wellness Clinic
Austin, Texas, 78712
United States

Collaborators and Investigators

Sponsor: University of Texas at Austin

  • Robin C Hilsabeck, PhD, PRINCIPAL_INVESTIGATOR, University of Texas Health Sciences Center at San Antonio

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-02
Study Completion Date2027-04-30

Study Record Updates

Study Start Date2024-02-02
Study Completion Date2027-04-30

Terms related to this study

Keywords Provided by Researchers

  • older adults
  • mild cognitive impairment
  • mild dementia
  • cognitive screening
  • primary care
  • dementia screening

Additional Relevant MeSH Terms

  • Cognitive Impairment
  • Dementia, Mild
  • Cognitive Decline