Home virtual-reality walking program for children with chronic conditions that affect physical health
Official title: EMMVIES : Walking Training at Home in VIrtual Reality for Children With Chronic Illnesses Impacting Physical Health
Run by University Hospital, Angers · NCT07021638 · Data updated 2026-11-12
This program tests whether a home-based virtual-reality walking training helps children aged 6–17 with conditions like cerebral palsy, neuromuscular disease, obesity, or heart disease improve walking and daily physical activity.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 6 Years to 17 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | University Hospital, Angers Government |
| Locations | 1 site (Angers) |
| Status | Recruiting |
| Started | December 24, 2025 |
| Main results expected | December 1, 2027 |
| Study ends | December 1, 2027 |
| Registry record updated | December 31, 2025 |
| Trial ID | NCT07021638 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children aged 6–17 who can walk for five minutes on a treadmill (with or without support), can use virtual-reality games and complete questionnaires, are enrolled in condition-specific care for at least six months, and meet subgroup criteria (e.g., CP GMFCS II–III or BMI above the IOTF-25 percentile for the obesity group).
✕Probably not a fit
Children who cannot walk for five minutes on a treadmill, who cannot engage with VR or questionnaires, or who have contraindications such as hip pathology in the obesity group are unlikely to benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The EMMVIES approach delivers a home-based walking training using virtual-reality games (immersive or non-immersive) on a treadmill, supported by parents, for children with chronic conditions that impair physical health. Participants must be able to walk for at least five minutes on a treadmill (with or without body-weight support or aids) and to engage with VR games and questionnaires. The protocol enrolls defined subgroups—children with cerebral palsy (GMFCS II–III), overweight/obese children aiming to increase activity, and children with neuromuscular or other chronic conditions—and integrates the program into ongoing condition-specific care. Initial setup and follow-up visits occur at the coordinating center in Angers, with the training sessions performed at home over the intervention period.
Why it matters
Potential benefit: If successful, the program could improve gait and daily physical activity while making rehabilitation more accessible by enabling prolonged home-based therapy.
How similar studies have gone: Home-based motor rehabilitation programs have shown feasibility and some small trials of treadmill or VR interventions report benefits, but large definitive evidence for broad pediatric chronic-condition populations is still limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient aged 6 to 17 years at date of inclusion; * Able to walk for 5 minutes on a treadmill with or without body weight support, with or without technical aids; * Be able to understand and play virtual reality games (immersive or non-immersive); * Be able to answer questionnaires; * Patient affiliated to or benefiting from a social security scheme; * Informed consent, dated and signed by parents or guardians (if minors), to participate in the study; * Included in a care program specific to their chronic condition for at least 6 months; * Meet the following criteria depending on the group: PC group: * Diagnosis of CP * Functional level classified II or III according to the Gross Motor Function Classification System (GMFCS) * Rehabilitation goal: improvement of gait and/or gross motor function OB group: * Overweight or obese, defined by a BMI above the IOTF-25 percentile * Aim to increase daily physical activity * No history of hip pathology Group NM: * Diagnosis of one of the following neuromuscular pathologies: spinal muscular atrophy type 3, Duchenne disease, congenital myopathy or Charcot Marie Tooth. * Functional level of grade 2 to 6 on the Walton scale, or grade 3 to 7 on the Vignos scale * Rehabilitation goal: improvement of walking and/or gross motor skills Exclusion Criteria: * Patients weighing over 100 kg (due to the technical constraints of using the AMY mat). * For children aged 6 to 11: in connection with the immersive virtual reality device: problems with stereoscopic vision (perception of images in 3 dimensions), unstabilized epilepsy, facial trauma \< 3 months, hearing or visual impairment, pain, dizziness or nausea caused by using immersive virtual reality. * Patients who have undergone surgery in the last 3 months; * Patients who have received intramuscular botulinum toxin injections in the lower limbs or intensive therapy in the 3 months prior to inclusion; * Patient with a non-routine therapeutic program planned within 5 months that could lead to confusion with the tested program; * Patient with insufficient understanding of the French language; * Patient opposition (child or adolescent); * Persons deprived of liberty by judicial or administrative decision; * Persons under compulsory psychiatric care; * Persons under legal protection;
Where it's running
-
Les Capucins
Angers, France Recruiting
Study contacts
- Study coordinator: Mickaël DINOMAIS, MD
- Email: Mickael.Dinomais@chu-angers.fr
- Phone: + 33 2 41 35 52 67
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.