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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02439853
Other study ID # STU00073634
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2013
Est. completion date January 2020

Study information

Verified date November 2022
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a study on Internet-based video-practice speech and language therapy for persons with primary progressive aphasia (PPA), behavioral-variant frontotemporal dementia (bvFTD), or related conditions.


Description:

The purpose of this study is: 1. To evaluate the effectiveness of speech and language therapy on a person's ability to communicate immediately after treatment, 6-months after treatment, and 12-months after treatment. 2. To identify the most effective speech and language therapy strategies for persons with these conditions. 3. To determine the feasibility of Internet-based video-practice of speech and language therapy for persons with these conditions. The study will involve 12 to 15 session over the course of 12 months. Some of these sessions will be in-person at the Northwestern Cognitive Neurology and Alzheimer's Disease Center (Chicago, IL), while others will take place over the Internet, using an online study portal.


Recruitment information / eligibility

Status Completed
Enrollment 57
Est. completion date January 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Diagnosis of dementia with language as a primary symptom (i.e. aphasia) - An informant who knows the participant well and can answer questions the participant's communication ability - Adequate hearing to follow conversation (correction permitted) - Adequate vision (correction permitted)

Study Design


Intervention

Behavioral:
Monthly Check-in Session
Subjects in the Check-In group will have an online session with a speech-language pathologist 3-, 4-, and 5-months from the subject's enrollment date.

Locations

Country Name City State
United States Northwestern University Chicago Illinois

Sponsors (5)

Lead Sponsor Collaborator
Northwestern University Alzheimer's Association, Illinois Department of Public Health, National Institutes of Health (NIH), The Association for Frontotemporal Degeneration

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of Functional Communication Abilities Functional Communication Abilities will be assessed through questionnaires about the participant's language and communication, neuropsychological testing, and speech and language therapy evaluations. Change from baseline assessment at 2-months, 6-months and 12-months post-treatment
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