RecruitingACTRN12616001582448

Speech treatment for spinocerebellar ataxia and Friedreich ataxia

Speech rehabilitation for dysarthria resulting from spinocerebellar ataxia or Friedreich ataxia


Sponsor

The University of Melbourne

Enrollment

30 participants

Start Date

Sep 1, 2016

Study Type

Interventional

Conditions

Summary

We have designed a home-based, intensive four week speech exercise program designed to improve speech in patients with spinocerebellar ataxia or Friedreich ataxia. The treatment protocol is based on principles of motor learning and neuroplasticity with a focus on improving intelligibility and vocal control. Exercises and feedback were created to enhance self-monitoring and include computer based aural, visual and results feedback and self-management.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing a home-based, intensive 4-week speech therapy program designed to improve speech clarity and vocal control in people with spinocerebellar ataxia or Friedreich ataxia — progressive neurological conditions that affect coordination, balance, and speech. The program uses computer-based exercises with audio, visual, and results feedback. Researchers hope this approach, based on principles of motor learning, will make speech more understandable. You may be eligible if: - You are 18 years of age or older - You have a genetically confirmed diagnosis of spinocerebellar ataxia (any type) OR Friedreich ataxia You may NOT be eligible if: - You do not have a genetically confirmed diagnosis of spinocerebellar ataxia or Friedreich ataxia Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Treatment involved a behavioural intervention designed to improve speech intelligibility and quality. Materials: Patients are provided with a laptop computer with treatment software installed, head

Treatment involved a behavioural intervention designed to improve speech intelligibility and quality. Materials: Patients are provided with a laptop computer with treatment software installed, head mounted USB microphone, treatment manual. Procedures: The program specifically targets prosody, vocal control and over-enunciation with the aim of improving overall speech intelligibility and confidence when communicating. It is based on principles of motor learning and neuroplasticity relating to practice conditions and bio-feedback. Phase I: Teaching and Establishment of treatment components The clinician introduces the goals and content of the therapy. Patients learn the skills needed to undertake the program and implementation of the exercises. Using the computer program will be reviewed and practiced together on the first visit. Phase II: Instatement and Rehabilitation A: Visual feedback: Visual feedback is provided through the real time loudness display. Patients can monitor the stability or variability of their loudness while speaking. For example, if patients cannot see any colour in the visual display they need to increase the loudness of their speech. Similarly, a stable production is required for the long vowel task, meaning the visual display should remain at a constant level throughout the production. The feedback given by the interface supports the patient by training self-awareness. Loudness is represented visually, providing an alternative mode of feedback other than listening. Demonstrate and encourage the use of these feedback options. B: Aural (listening) feedback: Patients are prompted to record parts of their speech each day. They are then required to listen to their recorded sample from the previous day. Listening feedback is designed to enhance self-monitoring and help the speaker identify aspects of their speech that need improvement. Listening to speech can be upsetting for some patients but it is a vital component of therapy. Delayed aural feedback is important for the development of self-monitoring skills by providing an opportunity to hear their performance, identify what worked and what went wrong and set some goals for the day. C: Outcome feedback: Patients are provided with immediate and objective feedback of their performance. Three pieces of information are derived from the recorded samples and compared against the previous days’ scores: 1. Duration, which is important for the long vowel task; 2-3. Loudness and pitch variation, both of which are important for the vowel and connected speech tasks. This information is designed to enhance the patient’s understanding of their performance and to provide a benchmark on which to compare earlier productions. Summary figures are provided at the end of each day after tasks are completed. The clinician will be able to plot your patients’ progress – highlighting the gains made during therapy. Therapy is completed in the home by the patient over 20 sessions within one month. Each session consists of excercises aiming to improve vocal quality and control, articulation, prosody and intelligibility. Self-evaluation skills are refined by the use of visual, aural and performance feedback and personalised problem-solving strategies. Clinicians monitor patient progress and provide support during this stage through weekly skype or phone calls. Who: Treatment is coordinated by the treating clinician and completed in the home or clinic by the patient. Treating clinicians are trained speech-language pathologists with a minimum of 5 years' experience; Mode of delivery: The first treatment session is conducted face to face. Each subsequent treatment day is conducted using the computer software. Adherence and progress is monitored weekly by the treating clinician via skype or telephone. Treatment is provided individually. Number of times: The intervention will be delivered 20 times over a 30-day period. Patients are required to complete therapy 5 days out of every 7 for the period of the study. Treatment sessions take approximately 45 minutes to complete. 20 x 45 minute sessions 5 times a week for 4 weeks.


Locations(3)

Monash Medical Centre - Clayton campus - Clayton

QLD,VIC, Australia

Royal Brisbane & Womens Hospital - Herston

QLD,VIC, Australia

Germany

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ACTRN12616001582448


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