Viewing Study NCT06546488



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06546488
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-07-12

Brief Title: Cognitive Assessment Tools for Huntingtons Disease
Sponsor: None
Organization: None

Study Overview

Official Title: Cognitive Assessment Tools for Individuals With Huntingtons Disease
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CAT-HD
Brief Summary: The purpose of the current proposal is to expand understanding of two currently available cognitive tools that are not typically used in Huntington Disease HD clinical trials that might be useful both for initial screening and for clinical trial application One is the Digit Symbol Coding Test DSC and the other is the Self-Administered Gerocognitive Examination SAGE Both the DSC and the SAGE have been used for assessments of individuals with other neurodegenerative diseases including Alzheimers Disease Parkinsons Disease and Lewy Body Disease but data is lacking on their use in individuals with HD
Detailed Description: Subjects will be recruited from the OSU Wexner Medical Center Huntington Society of America Center of Excellence Clinic Subjects will be scheduled for a one-time visit to complete the study The entire visit will take approximately 1-15 hours Vital signs weight blood pressure temperature respiratory rate and pulse will be conducted The subjects medical records will be reviewed to obtain their demographics current medications medicalsurgical HD family history and HD diagnosis details If any adverse events occur during the research visit they will be documented Participants will complete cognitive functional and motor assessments

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None