RECRUITING

Motor Imagery for Treatment Enhancement and Efficacy in Persons With Apraxia of Speech

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Treatment of post-stroke apraxia of speech (AOS) requires frequent and ongoing practice with a speech-language pathologist to facilitate lasting behavioral change, which is costly and, therefore, inaccessible to many patients. Thus, there is a critical need to identify novel, cost-effective ways to supplement speech therapy to increase opportunities for practice and optimize treatment outcomes. Our long-term goal is to develop an effective, home-practice, computer-based, motor imagery protocol Motor Imagery for Treatment Enhancement and Efficacy (MI-TEE) which will serve as an adjunct to routine speech therapy to optimize treatment response in persons with AOS. The overall objectives of this application are to (i) evaluate the acceptability and feasibility of MI-TEE as a home practice program and (ii) determine the efficacy of MI-TEE with speech therapy, compared to speech therapy alone, in improving speech production in people with AOS. Our central hypothesis is that MI-TEE will be an accessible, feasible, and efficacious adjunct to speech therapy. To attain our objectives, the following specific aims will be pursued using two single-subject experimental designs with multiple baselines across participants (n=18): 1) Evaluate the acceptability and feasibility of MI-TEE as an adjunct to speech therapy for the rehabilitation of AOS; and 2) Compare the efficacy of adjunctive MI-TEE plus standard speech therapy to standard speech therapy alone. Under the first aim, observational data, surveys, and semi-structured interviews will be employed to assess the acceptability (perceived satisfaction, appropriateness, and intent to continue use) and feasibility (recruitment, retention, and intervention adherence rates) of MI-TEE. For the second aim, accuracy of articulation for trained words and untrained words (generalization) will be measured pre-treatment, repeatedly during the treatment phase, and post-treatment. Improvements in speech accuracy will be documented using a binary scoring system (correct/incorrect). Multilevel analyses will be used to address rate of acquisition, overall change, and response variation across participants.

Official Title

Motor Imagery for Treatment Enhancement and Efficacy (MI-TEE) in Persons With Apraxia of Speech

Quick Facts

Study Start:2023-12-11
Study Completion:2026-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06467136

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Between the ages of 18 and 85 yrs. old
  2. * At least 6 months post left hemisphere stroke
  3. * Demonstrate AOS
  4. * Speak English as their primary language
  5. * Pass a hearing screening at 35 dB HL at 500, 1K, and 2K Hz for at least one ear
  6. * Normal or corrected to normal visual acuity
  1. * Unable to follow two-step commands and greater than moderate aphasia
  2. * Moderate - severe dysarthria
  3. * Untreated depression or other psychiatric illness
  4. * Degenerative neurological illnesses
  5. * Less than 3 on the MIQ-RS77
  6. * Less than a 4 on 3/5 domains on the FACETS
  7. * Less than a 23 on the Raven's Coloured Progressive Matrices
  8. * Receive other speech therapy while participating in the study

Contacts and Locations

Study Contact

Lauren Bislick Wilson, Ph.D.
CONTACT
407-823-4768
Lauren.Bislick@ucf.edu
Stephanie Eaton, MA
CONTACT
407-823-4768
Stephanie.Eaton@ucf.edu

Principal Investigator

Lauren Bislick Wilson, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Central Florida

Study Locations (Sites)

University of Central Florida Innovation Rehabilitation Center
Orlando, Florida, 32826
United States

Collaborators and Investigators

Sponsor: University of Central Florida

  • Lauren Bislick Wilson, Ph.D., PRINCIPAL_INVESTIGATOR, University of Central Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-11
Study Completion Date2026-07-31

Study Record Updates

Study Start Date2023-12-11
Study Completion Date2026-07-31

Terms related to this study

Keywords Provided by Researchers

  • Treatment of Apraxia of Speech
  • Home Practice for Apraxia of Speech
  • AOS
  • Apraxia of speech

Additional Relevant MeSH Terms

  • Apraxia, Oral
  • Apraxia of Speech