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Clinical Trials/NCT06211374
NCT06211374
Active, Not Recruiting
N/A

Communication Bridge: Optimizing an Evidence-based Intervention for Individuals With Primary Progressive Aphasia

University of Chicago1 site in 1 country12 target enrollmentJune 28, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Primary Progressive Aphasia
Sponsor
University of Chicago
Enrollment
12
Locations
1
Primary Endpoint
Change in Communication Participation Person Centered Goals
Status
Active, Not Recruiting
Last Updated
8 months ago

Overview

Brief Summary

The aim of this study is to evaluate the effectiveness and feasibility of evidence-based interventions in individuals living with mild to moderate primary progressive aphasia (PPA) that address communication-focused outcomes.

Detailed Description

The purpose of this study is to evaluate the effectiveness and feasibility of evidence-based interventions in individuals living with mild to moderate primary progressive aphasia (PPA) that address communication-focused outcomes. The study team aims to enhance the personal relevance and therapeutic impact of goal attainment scaling (GAS) while building self-efficacy within a self-management framework. This study will be a continuation of one of the largest non-pharmacologic intervention studies for individuals with PPA to date. It will add critical information regarding the effectiveness of telepractice interventions for communication disorders in adults with primary progressive aphasia specifically, and in dementia more broadly. The goal of this study is to maximize functional communication and life participation for the participants.

Registry
clinicaltrials.gov
Start Date
June 28, 2024
End Date
May 31, 2026
Last Updated
8 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • A dementia diagnosis other than Primary Progressive Aphasia
  • Participation is co-enrolled in an outside speech language therapy program during the study course.
  • Communication partners will be excluded if they have a pre-existing communication impairment that would affect study participation (e.g., aphasia, dementia) Medical records will be requested and reviewed to determine eligibility

Outcomes

Primary Outcomes

Change in Communication Participation Person Centered Goals

Time Frame: Time Frame: 2 assessment time points through study completion, an average of 5 months, including change over time

Goal Attainment Scaling, a 7-point rating scale with -3 representing 'no longer participating' and +3 representing 'exceeded goal'. Higher scores indicate better progress in goal achievement.

Study Sites (1)

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