Actively Recruiting
Educational Support Group Program for Carepartners of Bilingual and Spanish-speaking Persons With Progressive Forms of Aphasia and for Persons With Progressive Forms of Aphasia
Led by University of Texas at Austin · Updated on 2025-03-04
120
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
Sponsors
U
University of Texas at Austin
Lead Sponsor
T
The Association for Frontotemporal Degeneration
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate the benefits of an educational and support group program designed for individuals with progressive aphasia and their carepartners. The study focuses on people with progressive aphasia caused by various conditions, including Alzheimer's disease and other language-led dementias. It measures how participation in these groups affects psychosocial well-being, communication skills, and speech or language function through various assessments before, during, and after the program. Participants will join one of two group paths: a progressive aphasia educational/support group or a caregiver support group combined with a communication skills training phase involving their partner with aphasia. The caregiver group includes two phases: an educational/support phase with twice-monthly meetings for four months, and a practice phase with weekly sessions for one month. The progressive aphasia group participates only in the educational/support phase. The program is offered via telehealth, allowing participants from the United States and internationally to join. Participants engage in assessments before the program, immediately after each phase, and three months following treatment to track changes in communication, quality of life, mood, and caregiving impact. These include surveys, interviews, and standardized tests such as the Mini-Mental State Exam and Clinical Dementia Rating Scale. Researchers also monitor participation rates, homework completion, and retention. The total study duration is approximately nine months, including follow-up evaluations.
CONDITIONS
Brief Title
Educational Support Group Program for Bilingual and Spanish-speaking Carepartners and People With Progressive Aphasia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Speak Spanish and/or English
- Identify as Hispanic and/or Latinx, or have a spouse/family member with progressive aphasia who identifies as Hispanic and/or Latinx
- See and hear well enough to participate
- Have access to a computer or mobile device with video capability
- Have an internet connection
- Diagnosed with progressive aphasia or language-led dementia where aphasia significantly affects daily living
- Aware of language difficulties and willing to discuss them
- Able to engage actively in group discussions and activities with minimal support
- Able to attend meetings regularly
- Willing to follow support group rules for respectful interaction
- For caregiver support group: have a carepartner who consents to participate
- Carepartners must self-identify as caregivers, willing to discuss caregiving, attend meetings regularly, and follow respectful interaction rules
You will not qualify if you...
- No additional exclusion criteria beyond the inclusion requirements
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Duration - 4 months for the support group phase and 4 weeks for the implementation phase (if applicable)
Participants attend educational and support group meetings focusing on coping with language-led dementia or progressive aphasia, including discussion and education provided by experts. Caregiver participants may also engage in an implementation phase involving practice of strategies with clinician feedback.
Twice monthly meetings for 4 months for the support group; weekly meetings for 4 weeks for the implementation phase
Duration - 3 months
Participants complete follow-up evaluations at 3 months after finishing the treatment phases to assess outcomes and progress.
1 visit (in-person or virtual) at 3 months post-treatment
Trial Site Locations
Total: 1 location
1
University of Texas at Austin
Austin, Texas, United States, 78702
Actively Recruiting
Research Team
S
Stephanie M Grasso, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here