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CompletedNCT06936696Project PAIRUpdated Jul 23, 2026

Project PAIR: Parent-implemented Articulation Intervention With Recast

An interventional study of Broad Target Speech Recast and Traditional Speech Therapy in Hearing Impaired Children, sponsored by Vanderbilt University. Completed at 1 site in United States. Open to participants aged 4 Years to 10 Years. Per ClinicalTrials.gov, last updated 2026-07-23.

Sponsored by Vanderbilt University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
3
Allocation
Not applicable
Ages
4 Years to 10 Years
Sex
All
01

Study summary

Using a single-case multiple baseline across participants design, this study aims to explore the effectiveness of parent-implemented Broad Treatment Speech Recast supplemented with traditional clinician-led articulation therapy on speech production in elementary-aged deaf and hard of hearing children.

To address these objectives, the following research questions will be investigated:

  1. Does drill-based articulation therapy, administered by a speech-language pathologist, improve speech sound production in DHH children when parent-implemented BTSR is concurrently utilized at home?
  2. Does the combination of parent-implemented BTSR and clinician-led traditional articulation therapy result in generalization of speech sound accuracy at the conversation level?
02

Conditions studied

  • Hearing Impaired Children

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Keywords

  • deaf and hard of hearing
  • articulation
  • speech sound production
  • parent training
  • children
03

In context

Hearing Loss

1,092 studies on the registry are indexed under Hearing Loss; 235 are open to participants now.

This study's enrollment of 3 is below the median of 40 across 764 interventional studies indexed under Hearing Loss.

Browse Hearing Loss studies →

Lead sponsor

Vanderbilt University is the lead sponsor of 508 studies on the registry; 19 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 5 (71%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 10 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 4;0-9;11
  • Permanent, prelingual sensorineural hearing loss
  • Uses spoken English as their primary home language (≥ 51% of the time)
  • Standard score ≥70 on the Leiter
  • Standard score ≥70 on the OWLS-II Listening Comprehension
  • At least two speech sound errors appropriate to target based on speech norms and general stimulability

Exclusion criteria

Exclusion Criteria:

  • Motor speech disorder (e.g., childhood apraxia of speech)
  • Oral structural functional disorder (e.g., cleft palate)
  • Diagnosis of autism spectrum disorder
  • Diagnosis of ADHD
  • Uncorrected vision impairment (i.e., identified vision loss without the use of corrective lenses)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    Articulation Therapy

    Participants engage in two conditions: (1) Parent-implemented Broad Target Speech Recast (BTSR), (2) Parent-implemented BTSR combined with clinician-implemented speech therapy This is a nonconcurrent multiple probe single-case experimental design with staggered introduction of conditions across participants. All participants receive both interventions, but the interventions are introduced in separate phases and evaluated independently and in combination. This is not a crossover or parallel group design. Rather than having separate arms or randomization, each participant serves as their own control over time, allowing for individualized evaluation of intervention effects.

    Behavioral: Broad Target Speech Recast · Behavioral: Traditional Speech Therapy

Interventions

  • BehavioralBroad Target Speech Recast

    Broad Target Speech Recasts (BTSR) is a speech intervention technique in which an adult immediately recasts a child's incorrect articulation by providing a corrected version of the word in a naturalistic, meaningful context. Unlike traditional articulation therapy, which focuses on isolated sound drills, BTSR integrates correction seamlessly into conversation without requiring the child to repeat or imitate the model. This approach is rooted in principles of implicit learning, where repeated exposure to accurate speech models facilitates phonological development over time. BTSR differs from traditional minimal pair or phonetic placement techniques in that it does not involve explicit instruction or direct prompts for self-correction. Instead, it provides high-frequency, naturalistic exposure to correct phoneme production within functional language use.

    Also known as: BTSR

  • BehavioralTraditional Speech Therapy

    Traditional Speech Therapy is clinician-led and includes structured, drill-based approaches. Techniques such as placement cues, direct feedback, and reinforcement are used to help children achieve correct articulation. The structured nature of this approach is often more effective in remediating persistent speech errors than parent-implemented strategies alone. This study examines whether the combination of parent-implemented BTSR and clinician-led traditional articulation therapy leads to improved speech sound production and long-term maintenance of correct articulation in elementary-aged DHH children.

06

What researchers measure

Primary outcomes

  1. Target phoneme production accuracy

    The percent of accurate phoneme productions per target, which is derived by dividing the number of correct productions by the total possible points for each target and then multiplying by 100. Accurate phoneme production is defined by a speech-language pathologist's judgment of perceptual accuracy through the lens of broad transcription.

    Time frame: From baseline until end of treatment (when intervention criteria have been reached or 6 weeks of no progress / regression)

Secondary outcomes

  1. Goldman Fristoe Test of Articulation - Third Edition (GFTA-3)

    The Goldman-Fristoe Test of Articulation, Third Edition (GFTA-3) is a standardized assessment used to evaluate speech sound production in children, adolescents, and young adults (ages 2;0-21;11). It measures articulation skills by assessing a child's ability to produce consonant sounds in different word positions (initial, medial, final) and in connected speech. The test provides standard scores, percentile ranks, and age-equivalent scores. Scores are standardized with a mean of 100 and a standard deviation of 15. Standard scores range from 40 to 160, with higher scores indicating better articulation abilities.

    Time frame: Collected during eligibility (before the intervention) and at the end of the intervention (when intervention criteria have been reached or 6 weeks of no progress / regression)

  2. Generalization to Conversation

    Connected speech samples will involve a ten-minute conversation or play-based dialog initiated by the examiner or parent to elicit natural speech from the child. Various techniques may be employed to encourage a sample abundant in expressive language, including the use of open-ended questions and engagement in child-led pretend play. This task will occur at three time-points throughout the study (baseline, BTSR phase, after intervention criteria has been reached) to measure generalization, and it should be administered after the listening check and before the probe. This task will be captured on video for later analysis. Accuracy of phoneme targets will be calculated using percent of consonants correct.

    Time frame: From enrollment to the end of treatment (when child meets criteria or exhibits no progress/regression for three consecutive sessions).

07

Study locations

1 site
  • Vanderbilt University Medical Center
    Nashville, Tennessee 37232, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Mar 9, 2026
  • Informed consent form · Aug 15, 2024
  • Informed consent form · Mar 20, 2025

Documents are hosted by the registry — open the source record to download them.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06936696
Lead sponsor
Vanderbilt University
Responsible party
Meganne Muir (PhD Student and Certified Speech-Language Pathologist, Vanderbilt University) — Principal investigator
First posted
Apr 20, 2025
Start date
Jun 10, 2025
Primary completion
Jun 25, 2026
Completion
Jul 9, 2026
Last update
Jul 23, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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