Early Detection of Cognitive Decline — EDCD  

Cognitive Impairment Clinical Trial

Official title: Using the PROMIS Cognition Item Bank for Early Detection of Cognitive Decline in Primary Care

Status Completed

Clinical Trial Summary

The goal of this clinical trial is to evaluate the impact of a brief cognitive screener on provider behavior in patients completing an annual wellness visit (AWV). The main question[s] it aims to answer are:

• do appropriate referrals increase for patients using the new screener?

• do appropriate diagnostic orders increase for patients using the new screener? Participants will respond to 4 questions about their cognitive abilities as part of a larger AWV protocol.

Researchers will compare provider behavior for patients completing AWVs before and after implementation of the new screener to see if referral, diagnostic and prescribing behaviors differ.

Clinical Trial Description

In the course of this two-year project, the RAND team and partners (University of Pittsburgh Medical Center [UPMC] and Northwestern University [NU]) will conduct secondary data analysis to establish the validity of scores from the PCF item bank; use the resulting data to derive meaningful scoring criteria and interpretation guidance, and determine the best short form item set from the PCF item bank to use for standardized cognitive impairment screening during the Medicare Annual Wellness Visit (AWV); use qualitative methods to refine workflow for administering the screener in primary care; work with UPMC to integrate the resultant brief self-reported PROMIS cognition screener (PRO-CIS) into their workflows; and evaluate the effect of implementing brief standardized PRO-CIS with interpretive guidance on primary care providers' behaviors. ;

Related Conditions & MeSH terms

• Cognitive Dysfunction
• Cognitive Impairment

• NCT number: NCT05804981
• Study type: Interventional
• Source: RAND
• Status: Completed
• Phase: N/A
• Start date: June 8, 2022
• Completion date: January 19, 2024