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OpenTrials
Completed

NCT Number: NCT02752425

Visual Feedback of Tongue by Ultrasound Echography for Speech Trouble Rehabilitation

Speech is a privileged means of communication for humans: its trouble can thus prove being extremely handicapping. Standard speech therapy is limited in some cases by the lack of sensory feedback available to the patient (hearing, surgery, neural damage, etc.).

The present study aims at quantify the contribution of the tongue articulatory visual feedback offered by ultrasound echography to speech trouble rehabilitation.

Two complementary populations will be studied : 30 adults with buccopharyngeal surgery, and 10 childrens with important speech troubles due to central nervous system damage.

The principle is to conduct standard speech therapy sessions, alternating series of sessions with the use of visual feedback and sessions without visual feedback.

The progress will be regularly measured by means of standard batteries of speech articulation tests.

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Key information

Age range

8 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institut d'Education Motrice, Eybens, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Articulatory troubles needing speech therapy
  • French mother tongue
  • Adult patients [18 ≥ age < 80 years] who underwent buccopharyngeal surgery after cancer diagnostic OR children [8 ≥ age < 18 years] suffering from central nervous system damage

Exclusion criteria

  • Incapacity to easily understand the speech therapist instructions
  • People protected by the law
  • People deprived from freedom by judiciary decision
  • Potential allergy to the water-based conducting gel used to ensure good skin - probe contact
  • Overweight if large fatty mass under chin
  • Major edema under chin limiting echogenicity
  • Non corrected vision or hearing problems
  • For the adults: central or peripheral neural damage
  • History of Ear, Nose, and Throat surgery or radiotherapy
  • For the adults: isolated articulatory trouble, former articulatory trouble not treated, disfluency
  • Massive orofacial dyspraxia
  • Posture trouble
  • Motor problem in upper limbs

Treatment and study plan

Visual Feedback

Device

Use of ultrasound echography for tongue articulatory visual feedback

Primary outcomes

  1. BECD test score

    Time frame: 4 months

    One of the primary outcome will be measured as the difference of increase of total BECD score between the therapy sessions with and without visual feedback.

    BECD ("Batterie d'Evaluation Clinique de la Dysarthrie, Battery of Clinical Evaluation of Dysarthria") is a French speech articulation test.

  2. MBLF test score

    Time frame: 4 months

    The second primary outcome will be measured as the difference of increase of total MBLF score between the therapy sessions with and without visual feedback.

    MBLF ("Motricité Bucco-Linguo-Faciale, Motricity of Mouth, Tongue and Face") is a French speech articulation test.

Secondary outcomes

  1. Perception test scores

    Time frame: 4 months

    The secondary outcome will be measured as the difference of increase of the scores of perception obtained by a jury listening to a selected set of patients' speech sounds between the therapy sessions with and without visual feedback. The speech sounds are those recorded during the batteries of speech articulation tests.

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Acronym: REVISON

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Apr 27, 2016
Registry last updated
Sep 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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