Motor Imagery for Apraxia of Speech Treatment

This study is exploring a new way to help people with apraxia of speech (AOS) after a stroke. Apraxia of speech is a condition where your brain has trouble planning the movements needed for speech. The study is testing a home-based computer program called Motor Imagery for Treatment Enhancement and Efficacy (MI-TEE). This program uses 'motor imagery,' which is like mentally practicing speech movements. It will be used alongside a standard speech therapy called Sound Production Treatment. Researchers want to see if MI-TEE is acceptable and practical for participants, and if it helps improve speech. They plan to enroll 18 adults between 18 and 90 years old who have had a stroke at least 6 months ago, have AOS, and speak English.

Study design
This study is an interventional study planning to enroll 18 participants. It uses a mixed-methods design to evaluate the new treatment approach.
What's involved
Participants will complete an 8.3-week treatment program. They will also meet individually with a research team member after the program to complete surveys and interviews.
Compensation
Not stated in the trial record.
Follow-up
Acceptability will be assessed after the 8.3-week treatment program. Recruitment feasibility will be tracked through study completion, up to 24 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06467136

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

UNKNOWN
NAAges 18–90InterventionalTreatment
University of Central Florida
~18 participants
Updated 2025-06-26 on ClinicalTrials.gov
What's tested:Sound production treatmentMotor Imagery Practice

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Acceptability
Measured over Assessment of acceptability will occur after completion of the 8.3 week treatment program
+4 more outcomes measured
Apraxia, Oral
Apraxia of Speech
1 sites across 1 states
Florida1
  • Lauren Bislick Wilson, Ph.D. · PRINCIPAL_INVESTIGATOR · University of Central Florida

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

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

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
  • AcceptabilityAssessment of acceptability will occur after completion of the 8.3 week treatment program

    Participants will complete acceptability surveys and meet individually with a member of the research team to engage in semi-structured interviews.82 Acceptability data will include perceived satisfaction and appropriateness, experience with MI-TEE, and intent to continue use.

  • Recruitment feasibilityThrough study completion, up to 24 weeks.

    Feasibility data will be collected by research staff throughout the study and will include recruitment feasibility, the percent of eligible individuals agreeing to participate in the MI-TEE program.

  • Adherence ratesStart of MI-TEE program to the end of the 8.3 week treatment program for each participant.

    Feasibility data will be collected by research staff throughout the study and will include adherence rates, the participants ability to adhere to the MI-TEE protocol.

  • Retention rateStart of MI-TEE enrollment to the end of the 8.3 week treatment program for each participant.

    Feasibility data will be collected by research staff throughout the study and will include retention rates, the percent of participants who complete the entire MI-TEE program.

  • Rate of changeFrom enrollment to the end of maintenance at 10 weeks, total of up to 23 weeks.

    The dependent variable is rate of change for accuracy of sound production in experimental words produced during probes.