Skip to content

Treating Childhood Apraxia of Speech

Treating Childhood Apraxia of Speech: Role of Biofeedback & Practice Distribution

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03238677
Enrollment
56
Registered
2017-08-03
Start date
2017-08-01
Completion date
2022-06-07
Last updated
2023-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Apraxia of Speech

Keywords

speech sound disorder

Brief summary

The study will test two modifications to speech therapy for 40 school-age children with childhood apraxia of speech to determine how to improve treatment outcomes. The study will compare treatment that includes real-time visual feedback of the tongue during speech using ultrasound vs traditional therapy that does not include ultrasound visual feedback. Additionally, some children will be treated with a traditional schedule of 2 sessions per week, whereas others will be provided with treatment that begins with intensive training (10 hours of therapy in one week) and progresses to a more distributed treatment schedule.

Detailed description

Childhood apraxia of speech is a developmental speech sound disorder that may lead to persisting speech errors, often despite years of treatment. Such impairments may lead to social, academic, and vocational limitations. Thus, there is a need to explore alternate treatment approaches. This study will explore how to improve speech sound production in school-age children with CAS by modifying a standard speech therapy program. Two adaptations to speech therapy will be tested in a 2 x 2 randomized group design. In Aim 1, a standard treatment schedule of 2 one-hour sessions per week will be compared against a treatment sequence beginning with an intensive therapy schedule (10 hrs of treatment in one week), which will then transition to a more distributed practice schedule. This treatment modification is intended to minimize erred practice between training sessions in the early stages of learning, then foster generalization through increased time between practice sessions. In Aim 2, a standard treatment that includes only verbal feedback to the client during speech practice will be compared against a treatment sequence that initially includes real-time ultrasound visual feedback of the tongue during speech, which will be faded over the course of treatment. Ultrasound visual feedback is designed to train articulatory movements. It may enhance children's understanding of the articulatory goals of speech movement patterns by comparing executed tongue movements with intended movements. Prior case reports and single subject experimental designs have shown that speech sound production may be enhanced by including ultrasound visual feedback, although no prior randomized group studies have been conducted. Beside these modifications, the other aspects of treatment will be held constant. Outcomes will be evaluated by tracking changes in percent consonants correct from a large speech sample, scored by individuals who are blind to treatment status. The four groups will be compared to determine the extent to which speech sound therapy can be enhanced through a treatment sequence that begins with intensive practice and/or with ultrasound visual feedback.

Interventions

BEHAVIORALSpeech Motor Chaining without Biofeedback

These procedures target sound sequences (consonant-vowel, consonant-consonant, or vowel-consonant). Sessions begin with Pre-practice to elicit the target sounds, with verbal cueing and shaping strategies. The Practice component then includes chaining that is response-contingent. Participants practice in blocks of 6 consecutive trials beginning at the syllable level. If 5/6 are correct, the participant advances to monosyllabic word practice, then multisyllabic word practice, phrase practice, and sentence practice (with the target syllable embedded within each level of complexity). If fewer than 5/6 trials are correct, a different syllable with the target sound pattern is practiced next. Verbal feedback is faded from 5 of 6 trials at the syllable level to only 3 of 6 trials at the sentence level. For more description, see http://speechproductionlab.syr.edu/Resources%20for%20Researchers.html

BEHAVIORALBiofeedback

Real-time images of the tongue are made available using ultrasound placed beneath the chin. Participants practice speech movements and can be cued to modify their tongue shape or position to achieve clearer speech. Practice structure is similar to the Speech Motor Chaining procedures, but with the addition of a visual reference.

BEHAVIORALDistributed Practice

2 sessions per week for 10 weeks

BEHAVIORALMassed --> Distributed Practice

Week 1: 10 hours of treatment Week 2: 3 hours of treatment Week 3: 3 hours of treatment Week 4: 2 hours of treatment Week 5: 2 hours of treatment

Sponsors

National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH
Syracuse University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Individuals who conduct the phonetic transcriptions that will be used for the primary outcome data will be blinded as to whether the recordings were collected before or after treatment, and also blinded as to the group assignment of the participant.

Intervention model description

2 x 2 design Scheduling: Mass--\>Distributed vs. Distributed only Visual feedback: Sequenced Ultrasound Biofeedback vs. No biofeedback

Eligibility

Sex/Gender
ALL
Age
9 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Native English speakers who hear English as the dominant language in their home setting. * Must pass a hearing screening. * Score at or better than -2 standard deviations from the mean on the Matrix Reasoning Task of the Wechsler Abbreviated Scale of Intelligence - 2nd Edition (WASI-2; t-score ≥ 30), Peabody Picture Vocabulary Test - 4th Edition (PPVT-4; standard score ≥ 70), and the Following Directions subtest of the Clinical Evaluation of Language Fundamentals - 5th Edition (CELF-5; scaled score ≥ 3). * Goldman-Fristoe Test of Articulation - 3rd Edition (GFTA-3) percentile ≤ 5th). * A diagnosis of CAS will be verified based on a polysyllable picture naming task, diadochokinetic task (puh-tuh-kuh), and syllable repetition task.

Exclusion criteria

* Parent report or direct evaluation reveals oral-facial structural abnormalities (e.g., cleft palate). * Parental report of neurobehavioral disorders (e.g., autism spectrum disorders, ADHD, obsessive-compulsive disorder), or vision problems that are corrected with glasses/contacts. * Fail a hearing screening, or failure to meet criteria listed above as Inclusionary

Design outcomes

Primary

MeasureTime frameDescription
Speech Sound Accuracy10 weeks from the start of treatmentPercent consonants correct for target sounds: The primary outcome measure was percent correct for each participant's target sound-positions in untreated phrase. Participants imitated 20 pre-recorded phrases, each containing the target sound pattern 2 times per stimulus (e.g., for /l/ onset, leave the location), resulting in 40 attempts at each sound-position. For each session, 3 transcribers independently transcribed in Phon software (Hedlund & Rose, 2022) and accuracy was averaged across transcribers. Instances where IPA symbols for the Actual transcription differed from the Target transcription was scored as incorrect.

Countries

United States

Participant flow

Participants by arm

ArmCount
Biofeedback, Massed->Distributed, Face-to-Face
Sequenced biofeedback Mass Practice--\> Distributed Scheduling Biofeedback: Real-time images of the tongue are made available using ultrasound placed beneath the chin. Participants practice speech movements and can be cued to modify their tongue shape or position to achieve clearer speech. Practice structure is similar to the Speech Motor Chaining procedures, but with the addition of a visual reference. Massed --\> Distributed Practice: Week 1: 10 hours of treatment Week 2: 3 hours of treatment Week 3: 3 hours of treatment Week 4: 2 hours of treatment Week 5: 2 hours of treatment Modality: Face-to-Face
9
No Biofeedback, Distributed, Face-to-Face
Speech Motor Chaining with no biofeedback. 2 sessions/wk for 10 weeks Speech Motor Chaining without Biofeedback: These procedures target sound sequences (consonant-vowel, consonant-consonant, or vowel-consonant). Sessions begin with Pre-practice to elicit the target sounds, with verbal cueing and shaping strategies. The Practice component then includes chaining that is response-contingent. Participants practice in blocks of 6 consecutive trials beginning at the syllable level. If 5/6 are correct, the participant advances to monosyllabic word practice, then multisyllabic word practice, phrase practice, and sentence practice (with the target syllable embedded within each level of complexity). If fewer than 5/6 trials are correct, a different syllable with the target sound pattern is practiced next. Verbal feedback is faded from 5 of 6 trials at the syllable level to only 3 of 6 trials at the sentence level. Distributed Practice: 2 sessions per week for 10 weeks Modality: Face-to-Face
9
Biofeedback, Distributed, Face-to-Face
Sequenced biofeedback, 2 sessions/wk for 10 weeks Biofeedback: Real-time images of the tongue are made available using ultrasound placed beneath the chin. Participants practice speech movements and can be cued to modify their tongue shape or position to achieve clearer speech. Practice structure is similar to the Speech Motor Chaining procedures, but with the addition of a visual reference. Distributed Practice: 2 sessions per week for 10 weeks Modality: Face-to-Face
10
No Biofeedback, Massed-> Distributed, Face-to-Face
Speech Motor Chaining with no biofeedback. Mass Practice--\> Distributed Scheduling Speech Motor Chaining without Biofeedback: These procedures target sound sequences (consonant-vowel, consonant-consonant, or vowel-consonant). Sessions begin with Pre-practice to elicit the target sounds, with verbal cueing and shaping strategies. The Practice component then includes chaining that is response-contingent. Participants practice in blocks of 6 consecutive trials beginning at the syllable level. If 5/6 are correct, the participant advances to monosyllabic word practice, then multisyllabic word practice, phrase practice, and sentence practice (with the target syllable embedded within each level of complexity). If fewer than 5/6 trials are correct, a different syllable with the target sound pattern is practiced next. Verbal feedback is faded from 5 of 6 trials at the syllable level to only 3 of 6 trials at the sentence level. For more description, see http://speechproductionlab.syr.edu/Resources%20for%20Researchers.html Massed --\> Distributed Practice: Week 1: 10 hours of treatment Week 2: 3 hours of treatment Week 3: 3 hours of treatment Week 4: 2 hours of treatment Week 5: 2 hours of treatment Modality: Face-to-Face
9
No Biofeeedback, Distributed, Telepractice
Speech Motor Chaining with no biofeedback. 2 sessions/wk for 10 weeks Speech Motor Chaining without Biofeedback: These procedures target sound sequences (consonant-vowel, consonant-consonant, or vowel-consonant). Sessions begin with Pre-practice to elicit the target sounds, with verbal cueing and shaping strategies. The Practice component then includes chaining that is response-contingent. Participants practice in blocks of 6 consecutive trials beginning at the syllable level. If 5/6 are correct, the participant advances to monosyllabic word practice, then multisyllabic word practice, phrase practice, and sentence practice (with the target syllable embedded within each level of complexity). If fewer than 5/6 trials are correct, a different syllable with the target sound pattern is practiced next. Verbal feedback is faded from 5 of 6 trials at the syllable level to only 3 of 6 trials at the sentence level. Distributed Practice: 2 sessions per week for 10 weeks Modality: Telepractice
10
No Biofeedback, Massed->Distributed, Telepractice
Speech Motor Chaining with no biofeedback. Mass Practice--\> Distributed Scheduling Speech Motor Chaining without Biofeedback: These procedures target sound sequences (consonant-vowel, consonant-consonant, or vowel-consonant). Sessions begin with Pre-practice to elicit the target sounds, with verbal cueing and shaping strategies. The Practice component then includes chaining that is response-contingent. Participants practice in blocks of 6 consecutive trials beginning at the syllable level. If 5/6 are correct, the participant advances to monosyllabic word practice, then multisyllabic word practice, phrase practice, and sentence practice (with the target syllable embedded within each level of complexity). If fewer than 5/6 trials are correct, a different syllable with the target sound pattern is practiced next. Verbal feedback is faded from 5 of 6 trials at the syllable level to only 3 of 6 trials at the sentence level. For more description, see http://speechproductionlab.syr.edu/Resources%20for%20Researchers.html Massed --\> Distributed Practice: Week 1: 10 hours of treatment Week 2: 3 hours of treatment Week 3: 3 hours of treatment Week 4: 2 hours of treatment Week 5: 2 hours of treatment Modality: Telepractice
9
Total56

Baseline characteristics

CharacteristicBiofeedback, Massed->Distributed, Face-to-FaceTotalNo Biofeedback, Massed->Distributed, TelepracticeNo Biofeeedback, Distributed, TelepracticeNo Biofeedback, Massed-> Distributed, Face-to-FaceBiofeedback, Distributed, Face-to-FaceNo Biofeedback, Distributed, Face-to-Face
Age, Continuous10.31 years
STANDARD_DEVIATION 1
10.96 years
STANDARD_DEVIATION 1.9
11.16 years
STANDARD_DEVIATION 2.3
11.05 years
STANDARD_DEVIATION 2.4
10.0 years
STANDARD_DEVIATION 1.1
12.2 years
STANDARD_DEVIATION 2.1
10.85 years
STANDARD_DEVIATION 1.7
Ethnicity (NIH/OMB)
Hispanic or Latino
3 Participants9 Participants3 Participants0 Participants0 Participants2 Participants1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
6 Participants46 Participants6 Participants9 Participants9 Participants8 Participants8 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants1 Participants0 Participants1 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants1 Participants0 Participants0 Participants0 Participants1 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants9 Participants2 Participants3 Participants2 Participants1 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants1 Participants0 Participants1 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
9 Participants45 Participants7 Participants6 Participants7 Participants8 Participants8 Participants
Region of Enrollment
United States
9 participants56 participants9 participants10 participants9 participants10 participants9 participants
Sex: Female, Male
Female
3 Participants17 Participants2 Participants4 Participants3 Participants2 Participants3 Participants
Sex: Female, Male
Male
6 Participants39 Participants7 Participants6 Participants6 Participants8 Participants6 Participants
Speech Sound Accuracy20.2 Percent correct
STANDARD_DEVIATION 7.3
24.3 Percent correct
STANDARD_DEVIATION 7.8
35.5 Percent correct
STANDARD_DEVIATION 7.8
28.9 Percent correct
STANDARD_DEVIATION 8.1
23.2 Percent correct
STANDARD_DEVIATION 7.4
17.0 Percent correct
STANDARD_DEVIATION 4.3
21.2 Percent correct
STANDARD_DEVIATION 12.1

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
EG005
affected / at risk
deaths
Total, all-cause mortality
0 / 90 / 90 / 100 / 90 / 100 / 9
other
Total, other adverse events
0 / 90 / 90 / 100 / 90 / 100 / 9
serious
Total, serious adverse events
0 / 90 / 90 / 100 / 90 / 100 / 9

Outcome results

Primary

Speech Sound Accuracy

Percent consonants correct for target sounds: The primary outcome measure was percent correct for each participant's target sound-positions in untreated phrase. Participants imitated 20 pre-recorded phrases, each containing the target sound pattern 2 times per stimulus (e.g., for /l/ onset, leave the location), resulting in 40 attempts at each sound-position. For each session, 3 transcribers independently transcribed in Phon software (Hedlund & Rose, 2022) and accuracy was averaged across transcribers. Instances where IPA symbols for the Actual transcription differed from the Target transcription was scored as incorrect.

Time frame: 10 weeks from the start of treatment

ArmMeasureValue (MEAN)Dispersion
Biofeedback, Massed->Distributed, Face-to-FaceSpeech Sound Accuracy54.1 Percent correctStandard Error 13.5
No Biofeedback, Distributed, Face-to-FaceSpeech Sound Accuracy32.5 Percent correctStandard Error 14.1
Biofeedback, Distributed, Face-to-FaceSpeech Sound Accuracy26.8 Percent correctStandard Error 10.2
No Biofeedback, Massed-> Distributed, Face-to-FaceSpeech Sound Accuracy42.1 Percent correctStandard Error 11.1
No Biofeeedback, Distributed, TelepracticeSpeech Sound Accuracy32.50 Percent correctStandard Error 7
No Biofeedback, Massed->Distributed, TelepracticeSpeech Sound Accuracy43.0 Percent correctStandard Error 7.7
Comparison: Main effect of biofeedback at 10 weeksp-value: 0.13295% CI: [-23.2, 3.1]Mixed Models Analysis
Comparison: Main effect of Practice Distribution at 10 weeksp-value: 0.02895% CI: [-25.9, -1.5]Mixed Models Analysis
Comparison: Main effect comparing telepractice vs face-to-face treatmentp-value: 0.18795% CI: [-24.9, 5]Mixed Models Analysis
Comparison: Interaction of biofeedback and practice distribution at 10 weeksp-value: 0.12595% CI: [-5.8, 46.3]Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026