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Behavioral Intervention
Animal-Assisted Therapy for Aphasia (PATD Trial)
N/A
Waitlist Available
Led By Sharon M Antonucci, Ph.D.
Research Sponsored by Albert Einstein Healthcare Network
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Clinical diagnosis of aphasia acquired as the result of cerebro-vascular accident (CVA)
Be older than 18 years old
Must not have
Diagnosis of neurological injury or disease other than CVA
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediate arm: baseline, 6-weeks post baseline, 3 month follow-up; delayed arm: 2 baselines (6 weeks apart), 6-weeks post 2nd baseline, 3 month follow-up
Awards & highlights
No Placebo-Only Group
Summary
This trial studies how a PATD program can help people with aphasia (language loss due to stroke) gain confidence and social engagement, enabling them to live better lives.
Who is the study for?
This trial is for English-speaking adults with aphasia, a language impairment usually from stroke. Participants must understand the study, be willing and able to take part in activities, and live within an hour's drive of the research sites in Elkins Park or Philadelphia, PA.
What is being tested?
The study tests the Persons with Aphasia Training Dogs Program (PATD), which uses dog training techniques to improve confidence and social engagement for people living with aphasia.
What are the potential side effects?
Since this program involves animal-assisted therapy rather than medication, traditional side effects are not expected. However, participants may experience emotional fatigue or stress during training sessions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have speech difficulties due to a stroke.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a neurological condition that is not a stroke.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediate arm: baseline, 6-weeks post baseline, 3 month follow-up; delayed arm: 2 baselines (6 weeks apart), 6-weeks post 2nd baseline, 3 month follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediate arm: baseline, 6-weeks post baseline, 3 month follow-up; delayed arm: 2 baselines (6 weeks apart), 6-weeks post 2nd baseline, 3 month follow-up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change on Assessment of Living with Aphasia (ALA, Kagan et al., 2010)
Change on PI-adapted version of Pet Partners Animal-handler Evaluation.
Secondary study objectives
Change on Behavioural Assessment of Dysexecutive Syndrome (Wilson et al., 1996)
Cerebrovascular accident
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: ImmediateExperimental Treatment1 Intervention
Participants in this group will begin the training protocol immediately (within 1 week) after baseline pre-training evaluation is completed.
Group II: DelayedExperimental Treatment1 Intervention
Participants in the delayed arm will participate in two pre-training evaluations, one immediately upon enrollment and one at the end of the delay period immediately before beginning training
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Persons with Aphasia Training Dogs Program
2023
N/A
~20
Find a Location
Who is running the clinical trial?
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,049 Previous Clinical Trials
2,731,128 Total Patients Enrolled
Albert Einstein Healthcare NetworkLead Sponsor
64 Previous Clinical Trials
868,692 Total Patients Enrolled
Sharon M Antonucci, Ph.D.Principal InvestigatorAEHN
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I understand what is required of me in this research.I have speech difficulties due to a stroke.I am willing and able to follow the study's requirements.I have a neurological condition that is not a stroke.
Research Study Groups:
This trial has the following groups:- Group 1: Immediate
- Group 2: Delayed
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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