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Clinical Trials/NCT07330687
NCT07330687CompletedNot Applicable

A Brain Imaging Study of Abnormal Neural Network Reorganization Following Speech Training in Patients With Compensatory Articulation Secondary to Cleft Palate

Shufan Zhao1 site in 1 country164 target enrollmentStarted: January 6, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
164
Locations
1
Primary Endpoint
Change in Functional Connectivity of the Speech Related Network

Study Overview

Brief Summary

Cleft palate is one of the most common maxillofacial congenital malformations, which results in severe speech disorders. Compensatory articulation disorder, also known as non-oral articulation disorder (NOA), is considered as the major pathological change among these patients. However, the outcome of speech therapy, an important treatment method, for NOA is often unsatisfactory. This is attributed to the erroneous articulation patterns and entrenched habits in patients with NOA, which require considerable training intensity and time. According to preliminary results from the investigators' own study, as well as studies by others, structural and functional changes have been clearly identified in some brain regions of patients with NOA, suggesting that abnormal neural networks are involved in the progression of NOA. Thus, the investigators proposed the hypothesis that speech therapy effectively corrects articulation disorders through reconfiguration of pathological neural function and reorganization of the abnormal neural network involved in NOA. In this study, multimodal brain imaging techniques will be applied to investigate differences in brain functional connectivity and structural connectivity networks among groups with oral articulation (OA), varying degrees of NOA in postoperative cleft palate patients, and healthy controls. The relationship between improvement in speech intelligibility and alterations in brain networks before and after intervention will be compared. This study aims to reveal the neural network substrates associated with NOA and speech therapy. Overall, through this comprehensive study, the investigators aim not only to provide new insight into the underlying neural mechanism of NOA but also to accumulate evidence for improving the efficacy of speech therapy and discovering new therapeutic strategies in clinical practice.

Detailed Description

Cleft palate often leads to compensatory articulation disorder (Non-oral Articulation, NOA), which is resistant to conventional speech therapy. This study is grounded in the hypothesis that the efficacy of speech training is mediated by the reorganization of pathological neural networks and structures associated with NOA.

This non-randomized, longitudinal study employs a parallel-group design involving three cohorts: patients with NOA receiving speech training, postoperative cleft palate patients with normal oral articulation (OA) as a clinical control, and healthy controls. The primary objective is to identify the distinctive neural signatures (in both functional connectivity and brain structure) linked to NOA and its remediation through training.

All participants undergo multimodal magnetic resonance imaging (including high-resolution T1-weighted and resting-state functional scans) and standardized speech assessments at baseline. Only the NOA group then receives a structured speech training intervention, followed by post-intervention reevaluation. By comparing changes within and between groups, this study aims to disentangle neural alterations specific to NOA from those related to cleft palate in general.

The integrative analysis of brain-wide changes with a focus on speech-related regions is expected to provide a systems-level understanding of the neural mechanisms underlying NOA and treatment-induced recovery. The findings may contribute to the development of more effective, neuroscience-informed therapeutic strategies.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
4 Years to 16 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Aged between 4 and 16 years.
  • For patient groups: Diagnosed with non-syndromic cleft palate and having undergone cleft palate repair surgery at least 1 year prior.
  • For the NOA group: Diagnosed with compensatory articulation disorder (Non-oral Articulation, NOA) through standardized speech assessment.
  • For the OA group: Confirmed to have no compensatory articulation disorder (Oral Articulation, OA) through standardized speech assessment.
  • For the healthy control group: No history of any craniofacial malformations, speech disorders, or neurological diseases.
  • Participants and their legal guardians are able to understand and willing to provide written informed consent.
  • Able to cooperate with and complete magnetic resonance imaging (MRI) examinations (e.g., no claustrophobia, no contraindicated metal implants).

Exclusion Criteria

  • Presence of other known syndromes or cognitive impairments (e.g., autism spectrum disorder, intellectual disability).
  • History of other neurological diseases that may affect speech function (e.g., cerebral palsy, hearing loss).
  • Presence of severe other orofacial anomalies, or an unrepaired palatal fistula.
  • Contraindications for MRI examination (e.g., non-removable metal implants, severe claustrophobia).
  • Having received systematic speech therapy within the past 6 months.
  • Any other condition deemed by the investigator to be unsuitable for participation in the study.

Arms & Interventions

Non-Oral Articulation(NOA) group

Experimental

Participants receive the investigational behavioral intervention: Structured Speech Decompensation Therapy. This one-on-one therapy uses the glottal stop /kʔ/ as a key sound to guide correct articulation placement and correct compensatory habits, integrating multisensory cues. The intervention is administered by a certified speech therapist at a dosage of 1-hour sessions, with a frequency of 3 sessions per week, for a duration of 5 to 12 weeks. Parent participation in sessions and daily prescribed home practice are required components.

Intervention: Structured Speech Training for Decompensation (Behavioral)

Oral Articulation (OA) Group

No Intervention

Participants do not receive the investigational speech training intervention. This arm serves as the clinical control group.

healthy control(HC)

No Intervention

Participants do not receive any study-related intervention. This arm serves as the healthy normative control group.

Outcomes

Primary Outcomes

Change in Functional Connectivity of the Speech Related Network

Time Frame: From baseline assessment to post-training assessment (approximately at Week 12)

Change in resting-state functional connectivity, focusing on connections between pre-defined speech-related regions (Broca's and Wernicke's areas) and additionally assessed through whole-brain network analysis, using resting-state fMRI data.

Change in Percent Correct Consonants (PCC)

Time Frame: From baseline assessment to post-training assessment (approximately at Week 12)

Change in the percentage of consonants produced correctly, assessed within both single-word and conversational speech contexts. The measure is derived from standardized speech samples, which are evaluated by blinded, certified speech-language pathologists.

Secondary Outcomes

  • Change in Proportion of Compensatory Articulation Errors(From baseline to post-training assessment (at Week 12))
  • Change in Grey Matter Volume (GMV) of Articulation-Related Regions(From baseline to post-training assessment (at Week 12))
  • Change in Regional Homogeneity (ReHo) in Speech-Related Cortex(From baseline to post-training assessment (at Week 12))
  • Change in Amplitude of Low-Frequency Fluctuations (fALFF)(From baseline to post-training assessment (at Week 12))
  • Change in White Matter Volume (WMV) of Articulation-Related Regions(From baseline to post-training assessment (at Week 12))

Investigators

Sponsor
Shufan Zhao
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Shufan Zhao

PhD, Attending Physician

Wenzhou Medical University

Study Sites (1)

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