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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorUniversity of Central Florida

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Unable to follow two-step commands and greater than moderate aphasia

Moderate - severe dysarthria

Untreated depression or other psychiatric illness

Degenerative neurological illnesses

Trial design

Design model

Parallel

Treatments tested in this trial

  • Sound production treatment

    Behavioral

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

  • Motor Imagery Practice

    Behavioral

    Practice of target items using motor imagery during home practice

Treatment groups

18 Participants
are divided into 2 treatment groups
Group A: Condition 1Experimental treatment 2 interventions
Group B: Condition 2Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Acceptability

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.

Time frame
Assessment of acceptability will occur after completion of the 8.3 week treatment program
2

Recruitment feasibility

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.

Time frame
Through study completion, up to 24 weeks.
3

Adherence rates

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.

Time frame
Start of MI-TEE program to the end of the 8.3 week treatment program for each participant.
4

Retention rate

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.

Time frame
Start of MI-TEE enrollment to the end of the 8.3 week treatment program for each participant.

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Central Florida

Lead sponsor

National Institutes of Health (NIH)

Collaborator

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborator