Could virtual reality help kids with a rare muscle disease read emotions better?
NCT ID NCT05916677
First seen Jun 29, 2026 · Last updated Jun 30, 2026 · Updated 1 time
Summary
This study tests whether virtual reality training can help children aged 6 to 16 with the childhood form of myotonic dystrophy type 1 (DM1) improve their ability to understand others' thoughts and emotions. Participants engage in social scenarios in a virtual environment, guided by an experimenter who asks questions and provides feedback. The goal is to see if this approach can strengthen social skills that are often affected in DM1.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual reality training
- What this could lead to
- If it works, this could offer a new way to help children with DM1 better understand social situations and emotions, improving their daily interactions.
- What could go wrong
- This is a small, early-stage study with only 35 participants, so results may not apply to everyone. The training may not lead to lasting improvements.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
35 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
-
Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
6 to 16 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 6 years and \< 16 years of age * Written informed consent * Affiliate or beneficiary of a social security scheme * Able to comply with all protocol requirements * Infantile form of DM1 with molecular confirmation. * Development without incident in the first year * Normal development in the pre and neonatal period * Native language French Exclusion Criteria: * Unable to participate in the study * Inability to comply with protocol requirements * Congenital form of DM1 * IQ\<70 (Intellectual Disability)
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Myotonic dystrophy type 1, infantile form are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Institut de Psychologie
Boulogne-Billancourt, 92000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Scientists hunt for biomarkers to unlock DM1 treatments
- No travel needed: new study uses video calls to uncover genetic secrets of childhood muscle disease
- Brain scans reveal diabetes link to cognitive decline in rare disease
- New study aims to uncover why people with muscle disease fall
- Heart risk study for muscular dystrophy patients completed
- Music therapy tested for rare muscle disease in kids