RecruitingACTRN12624001252505

Swallowing Therapy in People with Parkinson’s Disease using Principles of Motor Learning and Ultrasound Biofeedback

Effect of Swallowing Therapy on efficiency of eating and drinking in People with Parkinson’s Disease using Principles of Motor Learning and Ultrasound Biofeedback


Sponsor

The University of Sydney

Enrollment

6 participants

Start Date

May 14, 2025

Study Type

Interventional

Conditions

Summary

Dysphagia (i.e., swallowing difficulties) is common among people with Parkinson’s Disease (PwPD). Parkinson’s Disease results in movements that are smaller and slower than desired. There is limited research evidence on intervention options that improve tongue movement patterns in PwPD. This study aims to develop and test an intervention program that works on improving tongue movement patterns when eating and drinking with the use of ultrasound visual feedback and principles of motor learning. The study will use a single case experimental design to determine the effectiveness of the developed intervention in reducing the time taken to eat and drink as well as its impact on quality of life in PwPD. The hypothesis is that PwPD with dysphagia who participate in a four-week intervention using ultrasound visual feedback and principles of motor learning will show improvements in their swallowing efficiency.


Eligibility

Sex: Both males and femalesMin Age: 50 Yearss

Plain Language Summary

Simplified for easier understanding

Parkinson's disease affects movement throughout the body, including the muscles involved in swallowing. Many people with Parkinson's disease develop swallowing difficulties — known as dysphagia — which can affect how safely and efficiently they eat and drink. This study is developing and testing a new therapy that uses real-time ultrasound images of the tongue to give people visual feedback while they practise swallowing exercises. Participants take part in a four-week intervention where a speech pathologist uses an ultrasound device placed under the chin to show patients what their tongue is doing during swallowing. Seeing this feedback in real time can help people learn to move their tongue more effectively — similar to how watching yourself in a mirror can improve a physical skill. The study uses a design called single case experimental design, which carefully tracks each person's progress over time. You may be eligible if you are 50 or older, have been diagnosed with Parkinson's disease by a neurologist, have noticed changes in your swallowing in the past year, and live independently in the community. Participants should be medically stable and able to communicate in English.

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

Intervention Name: Swallow Therapy with Ultrasound Biofeedback In this approach, an ultrasound probe will be placed under the participant’s chin and a real time video image of the tongue within the

Intervention Name: Swallow Therapy with Ultrasound Biofeedback In this approach, an ultrasound probe will be placed under the participant’s chin and a real time video image of the tongue within the mouth will be seen while the participant is eating or drinking. This approach is referred to as ultrasound biofeedback. The intervention will consist of swallowing liquids or food with ultrasound biofeedback on the tongue movement pattern while swallowing. This is an individual intervention and will be delivered three times a week across four weeks. Each intervention session will take approximately 45-60 minutes and involve up to 50 swallows (either fluid, food, or saliva swallows). The intervention will be conducted face to face by a speech pathologist with more than five years of experience in managing swallowing difficulties. The intervention will take place at either the University of Sydney SPEECH Clinic or the participant’s home within metropolitan Sydney at a mutually convenient time. No home practice is required. The intervention will be individually titrated in terms of (a) frequency and duration of the treatment sessions, (b) the duration and frequency of breaks provided (c) the type of foods and fluids used, (d) the amount and type of feedback provided and (e) the number of times the participant is asked to swallow. These components will be altered based on participants’ fatigue level and response to the intervention protocol. Participant’s fatigue level will be monitored during each intervention session while the participant’s response to the therapy protocol will be reviewed on the 1st intervention session each week. To maintain treatment fidelity, intervention will be conducted as per a pre-written intervention protocol. Treatment fidelity will be reviewed by an independent speech pathologist for a random 20% selection of intervention sessions during the study using a checklist to ensure adherence to the intended protocol.


Locations(1)

NSW, Australia

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