ALS Amyotrophic Lateral Sclerosis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Control group: - Age 18 or older (between 45 - 75 years for the subgroup of controls that will be compared to the patient group, see chapter 4.1 ) - Blank neurological history - Adequate proficiency in Dutch and/or English language Patient group: - Age 18 or older - A diagnosis with bulbar onset ALS or PLS - A strongly impaired ability to speak - Ability to lie flat on the scanner bed for the duration of the fMRI scan (approximately 60 minutes) without respiratory difficulties or significant saliva build-up - Ability to press emergency button in the scanner with the hand - A score of at least 70% on the protocol understanding verification questionnaire - Adequate proficiency in Dutch and/or English language
Exclusion criteria
Exclusion criteria: General: - Noncompliance with MRI safety check list - Claustrophobia - Pregnancy - Inability to hear the instructions presented orally in the scanner without a hearing aid Patient group: - Mechanical ventilation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The three study parameters/endpoints are: 1) decoding (classification accuracy) of silently spoken or attempted words from the brain area that represents the articulation of speech in both ALS or PLS patients and healthy controls. 2) The fMRI brain activity pattern related to articulator movements (movement direction and amplitude); 3) The movement trajectories of the articulators during speech production 4) The fMRI brain activity patterns related to the production of phonemes 5) The fMRI brain activity pattern related to different combinations of sequences of the same phonemes within a word. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study parameters are the optimal acquisition parameters necessary to discriminate different words based on fMRI activity from the brain area representing articulation of speech. | — |
Countries
Netherlands