Recruiting

Motor Imagery

Sponsor:

University of Central Florida

Code:

NCT06467136

Conditions

Apraxia, Oral

Apraxia of Speech

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Sound production treatment

Motor Imagery Practice

Study Details

Brief summary:

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.

Conditions

Apraxia, Oral

Apraxia of Speech

Study ID

NCT06467136

Start date

Dec 11, 2023

Status verified date

Jun, 2024

Completion date

Jul 31, 2026

Anticipated

Primary completion date

Jul 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Between the ages of 18 and 90 yrs. old
  • At least 6 months post left hemisphere stroke
  • Demonstrate AOS
  • Speak English as their primary language
  • Pass a hearing screening at 35 dB HL at 500, 1K, and 2K Hz for at least one ear
  • Normal or corrected to normal visual acuity

Exclusion Criteria:

  • Unable to follow two-step commands and greater than moderate aphasia
  • Moderate - severe dysarthria
  • Untreated depression or other psychiatric illness
  • Degenerative neurological illnesses
  • Less than 3 on the MIQ-RS77
  • Less than a 4 on 3/5 domains on the FACETS
  • Less than a 23 on the Raven's Coloured Progressive Matrices
  • Receive other speech therapy while participating in the study

Study Design

Enrollment

18 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Condition 1

Condition 1 will have three phases: (A) no treatment; (B) speech therapy alone; (C) speech therapy plus MI-TEE (the home practice program).

experimental: Condition 2

Condition 2 will include two phases: (A) no treatment; (C) speech therapy plus MI-TEE (the home practice program).

Interventions

Sound production treatment

Evidence based treatment for apraxia of speech, developed by Julie Wambaugh.

Motor Imagery Practice

Practice of target items using motor imagery during home practice

Primary outcome measure

  • Acceptability [ Time Frame: Assessment of acceptability will occur after completion of the 8.3 week treatment program ]
  • Recruitment feasibility [ Time Frame: Through study completion, up to 24 weeks. ]
  • Adherence rates [ Time Frame: Start of MI-TEE program to the end of the 8.3 week treatment program for each participant. ]
  • Retention rate [ Time Frame: Start of MI-TEE enrollment to the end of the 8.3 week treatment program for each participant. ]
  • Rate of change [ Time Frame: From enrollment to the end of maintenance at 10 weeks, total of up to 23 weeks. ]

Central Contacts and Locations

Central contacts

Locations

University of Central Florida Innovation Rehabilitation Center

Recruiting

Orlando, Florida, United States, 32826

Contacts

Principal Investigator:

Lauren Bislick Wilson, PhD

More Information

Sponsor

University of Central Florida

Last update posted

Jun 26, 2025

Last verified

Jun, 2024

Keywords

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

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Central Florida on 2025-06-26.