Delayed Auditory Feedback Impact on Subtypes of Progressive Apraxia of Speech

Overview

About this study

The purpose of this study is to evaluate the impact of delayed auditory feedback in subtypes of progressive apraxia of speech.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Adult (18 years or older).
Able to provide samples in English.
US based patient.
Ability to provide informed consent.

Exclusion Criteria:

Unable to provide samples in English.
Nonverbal /No speech.
High Profile Patient (HPP) Status.
International patient.
Lack the ability to consent for themselves.
Unable to access the web-based application.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 5/19/23. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Rochester, Minn. Mayo Clinic principal investigator Rene Utianski, Ph.D.	Open for enrollment	Contact information: Ashley Bachman (507) 284-0695 Bachman.Ashley@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

Rene Utianski, Ph.D.

Open for enrollment

Contact information:

Ashley Bachman

(507) 284-0695

Bachman.Ashley@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials