VR meditation study for ALS patients withdrawn before starting
NCT ID NCT05409508
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to see if mindfulness meditation using virtual reality could help people with ALS feel better emotionally and improve their quality of life. It was designed for adults with ALS who speak French. However, the study was withdrawn before enrolling any participants, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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.
- Expected to start
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May 2022
An estimate. Start dates often move.
- Expected to finish
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Jun 2023
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Majors to inclusion * Mother tongue: French * Patients for whom ALS of bulbar or spinal form defined according to El Escorial criteria is possible, probable or certain * Able to carry out the investigations and interventions provided for in the protocol * Signature of informed consent to participate in the study Exclusion Criteria: * Participation in intervention research modifying management * History likely to disrupt cognition (constituted stroke, sequelae of traumatic brain injury, active epilepsy, learning disabilities, alcohol dependence syndrome, drug use, psychiatric disorders), severe cognitive impairment (MMSE \<24) * People who meet the diagnostic criteria for Frontotemporal Dementia * Pregnant or lactating women * Persons deprived of their liberty by administrative or judicial decision * Persons undergoing psychiatric care under duress * Persons subject to a legal protection measure * Persons unable to express their consent * Persons not affiliated or not beneficiaries of a social security scheme
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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.
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Other studies related to the condition(s) this trial covers.
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