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Profile of Dysphagia in Myotonic Dystrophy Type 1 (DM1)

A Multidimensional Profile of Dysphagia in People Living With Myotonic Dystrophy Type 1 (plwDM1)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05865483
Acronym
SwallowDM1
Enrollment
177
Registered
2023-05-18
Start date
2023-07-03
Completion date
2024-08-23
Last updated
2025-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysphagia, Oropharyngeal, Myotonic Dystrophy 1

Brief summary

The goal of this observational study is to learn about swallowing difficulties (dysphagia) in patients living with myotonic dystrophy type 1 (DM1). The main questions it aims to answer are: * whether the size and structure of the muscles involved in swallowing differ to those without the disease * how the size and structure of muscles may associate with swallowing function and swallowing symptoms in this group. Participants will undergo a range of tests including: * Ultrasound (US) assessment of the muscles involved in swallowing * An x-ray swallowing study (known as videofluoroscopy) * Assessment of swallowing symptoms, including questionnaires * Assessments of mobility, activity and breathing * Assessments of quality of life and wellbeing

Detailed description

This study will explore swallowing difficulties (dysphagia) caused by Myotonic Dystrophy Type 1 (DM1). Dysphagia causes food, drink and saliva to travel onto the lungs (aspiration) and can lead to pneumonia. Aspiration pneumonia is frequent and accounts for over 40% of deaths in DM1. Dysphagia also causes fear and anxiety which can lead to permanent lifestyle changes. A better understanding of dysphagia in DM1 will improve our assessment and treatment and reduce its life-changing consequences. This research aims to define the dysphagia profile of people with DM1 (pwDM1) across the domains of structure, function, experience, and wellbeing by: 1. Investigating the size and structure of muscles involved in swallowing in patients with and without DM1. 2. Exploring how muscle size and structure are associated with i) swallowing function and ii) symptoms 3. Exploring how swallowing function is associated with i) symptoms, ii) patient and caregiver wellbeing and iii) other aspects of DM1 such as walking and breathing. People aged 18+ with a confirmed diagnosis of DM1 will be invited to take part. Approximately 90 pwDM1 will be recruited. They will undergo a battery of tests including: * Ultrasound (US) assessment of the muscles involved in swallowing * An x-ray swallowing study (known as videofluoroscopy) * Assessment of swallowing symptoms, including questionnaires * Assessments of mobility, activity and breathing * Assessments of quality of life and wellbeing A sub-group of 20 pwDM1 will also undergo magnetic resonance imaging (MRI) of the muscles involved in swallowing to examine in detail the changes in seen on ultrasound. Approximately 60 people without DM1 will act as a control group for the US assessments. Primary caregivers of those with DM1 will be invited to complete a wellbeing questionnaire. Data will be analysed using statistical methods and findings will be used to develop clinical practice recommendations for the assessment and treatment of dysphagia in DM1. This study is part of an NIHR-funded clinical doctoral research fellowship (CDRF) and will take place at The National Hospital for Neurology and Neurosurgery (NHNN) in London. The maximum timescale for the study from opening recruitment to data collection of the final participant is 18 months (approx. 1st April 2023 - 30th September 2024).

Interventions

None listed

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
Myotonic Dystrophy Support Group, United Kingdom
CollaboratorUNKNOWN
The National Brain Appeal, The National Hospital for Neurology and Neurosurgery
CollaboratorUNKNOWN
University College, London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants with DM1 Inclusion: * ≥18 years of age * genetically confirmed of DM1 * able to eat & drink at least five sips of liquid by mouth at one time. Exclusion: * any condition or treatment other than DM1 that potentially influences swallowing muscle composition or function (e.g., a history of stroke or throat cancer). * any patients who are pregnant * patients with congenital or childhood DM1 * patients who are not able to eat or drink anything by mouth.

Design outcomes

Primary

MeasureTime frame
Swallowing muscle (geniohyoid) size16 months
Swallowing muscle (geniohyoid) structure16 months

Secondary

MeasureTime frame
Association between muscle (size and structure) and dynamic swallowing assessment (VFSS)16 months
Association between muscle (size and structure) and strength (Iowa Oral Performance Instrument & bite-force)16 months
Association between muscle (size and structure) and swallowing speed (timed water swallow test & timed test of mastication)16 months
Association between muscle (size and structure) and patient symptoms (Sydney Swallow Questionnaire & SWAL-QOL)16 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026