Informations générales
  • Catégorie de maladie Maladies du système nerveux (BASEC)
  • Study Phase N/A (ICTRP)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Berne
    (BASEC)
  • Responsable de l'étude Mario Sousa mario.sousa@insel.ch (BASEC)
  • Source(s) de données BASEC: Importé de 17.03.2025 ICTRP: Importé de 25.04.2025
  • Date de mise à jour 25.04.2025 02:00
HumRes61071 | SNCTP000005270 | BASEC2022-01304 | NCT05765110

Language as an Indicator of Emotions, Motor Skills, and Cognition in Patients with Parkinson's Disease

  • Catégorie de maladie Maladies du système nerveux (BASEC)
  • Study Phase N/A (ICTRP)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Berne
    (BASEC)
  • Responsable de l'étude Mario Sousa mario.sousa@insel.ch (BASEC)
  • Source(s) de données BASEC: Importé de 17.03.2025 ICTRP: Importé de 25.04.2025
  • Date de mise à jour 25.04.2025 02:00

Résumé de l'étude

Parkinson's disease affects mobility, thought processes, and mood. Our language is one of the most complex programs of humans. It simultaneously contains information about mobility, thinking, and mood. These three levels of mobility, thinking, and mood are subject to spontaneous fluctuations and can be influenced by external stimuli such as emotionally charged images. Furthermore, these three levels are influenced on one hand by Parkinson's disease itself and on the other hand by its treatment with medications or deep brain stimulation (DBS). For this reason, we want to study the language of Parkinson's patients in great detail regarding motor, cognitive, and emotional elements using computer-assisted methods for better therapy management. With this study, we aim to investigate whether computer-assisted speech analysis can reliably and objectively capture the fluctuations of mobility, mood, and thinking in Parkinson's patients. Even in healthy individuals, language changes depending on the situation, which is why we also want to include healthy subjects as a control group.

(BASEC)

Intervention étudiée

- Parkinson's patients without deep brain stimulation will undergo examinations; 1) once without Parkinson's medications (when the effect of the medications wears off), the so-called OFF state and 2) once with Parkinson's medications, when the medications are working optimally (ON state). - Parkinson's patients with deep brain stimulation (DBS) will undergo examinations without the influence of Parkinson's medication (OFF state); 1) once with DBS stimulation turned on (ON stimulation) and 2) once with DBS stimulation turned off (OFF stimulation). Furthermore, the examinations will be repeated in the medication ON state (with regular Parkinson's medication); 3) once with stimulation turned on (ON stimulation) and 4) once with stimulation turned off (OFF stimulation). Healthy individuals from the control group will undergo the examinations only once.

(BASEC)

Maladie en cours d'investigation

This research project includes Parkinson's patients with and without deep brain stimulation (DBS). Additionally, healthy individuals will also be recruited for the control group, who are in good general health and do not suffer from Parkinson's disease or any other neurological or psychiatric condition.

(BASEC)

Critères de participation
Parkinson's patients: - Age between 30-75 years - Parkinson's patients treated without or with deep brain stimulation (in the subthalamic nucleus) - Fluent in German or French (written and spoken) Control group (healthy subjects): - All individuals fluent in German or French between 50-70 years, who are in good general health. (BASEC)

Critères d'exclusion
Parkinson's patients: - Speech disorder caused by conditions other than Parkinson's - Clinical diagnosis of a speech disorder (aphasia) - Psychiatric conditions or other conditions affecting the brain - Inability to follow the study procedures, e.g., due to speech problems, mental disorders, or dementia Control group (healthy subjects): - Individuals suffering from Parkinson's disease or another neurological or psychiatric condition (BASEC)

Lieu de l’étude

Berne

(BASEC)

Czechia, Switzerland (ICTRP)

Sponsor

Insel Gruppe AG, University Hospital Bern

(BASEC)

Contact pour plus d'informations sur l'étude

Personne de contact en Suisse

Mario Sousa

+41 31 66 4 23 49

mario.sousa@insel.ch

Insel Gruppe AG, University Hospital Bern

(BASEC)

Informations générales

Insel Gruppe AG, University Hospital Bern

31 66 4 03 7131 66 4 03 71

mario.sousa@insel.ch

(ICTRP)

Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)

Commission cantonale d'éthique de Berne

(BASEC)

Date d'approbation du comité d'éthique

09.12.2022

(BASEC)


Identifiant de l'essai ICTRP
NCT05765110 (ICTRP)

Titre officiel (approuvé par le comité d'éthique)
SPEECH as Biomarker for Emotion, Movement and cOgnition in Parkinson's Disease (EMO-SPEECH-PD) (BASEC)

Titre académique
SPEECH as Biomarker for Emotion, Movement and cOgnition in Parkinson's Disease (ICTRP)

Titre public
SPEECH as Biomarker for Emotion, Movement and cOgnition in Parkinson's Disease (ICTRP)

Maladie en cours d'investigation
Parkinson Disease (ICTRP)

Intervention étudiée
Other: Dopaminergic OFF drug stateOther: DBS OFF stateOther: Dopaminergic ON drug stateOther: DBS ON state (ICTRP)

Type d'essai
Interventional (ICTRP)

Plan de l'étude
Allocation: Non-Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label). (ICTRP)

Critères d'inclusion/exclusion
Patients with Parkinson's Disease

Inclusion Criteria:

- Written informed consent

- Idiopathic PD according to the Movement Disorders Society Criteria

- Age of participants > 30 and = 75 years

- Treatment with or without bilateral deep brain stimulation in the subthalamic
nucleus

- Fluent in German or French

Exclusion Criteria:

- Dysarthria caused in addition by a condition other than PD (e.g. stroke,
myasthenia)

- Clinical diagnosis of aphasia

- Brain disease other than Parkinson's disease (e.g. atypical Parkinsonism,
Alzheimer's disease, vascular dementia, multiple sclerosis, stroke, traumatic brain
injury, epilepsy, etc.).

- Cognitive impairment (Montreal Cognitive Assessment (MoCa) < 24/30 points)

- Depression with acute suicidal ideation

Healthy Controls

Inclusion Criteria:

- Written informed consent

- Adults from 50-70 years old

- Fluent in German or French

Exclusion Criteria:

- Diagnosis of Parkinson's disease

- Cognitive impairment (Montreal Cognitive Assessment (MoCa) < 24/30 points)

- Suffering from brain disease (e.g. atypical Parkinsonism, Alzheimer's disease,
vascular dementia, multiple sclerosis, stroke, traumatic brain injury, epilepsy,
etc.)

- Clinical diagnosis of aphasia, dysarthria, and stuttering

- Suffering from or diagnosed with psychiatric illnesses according to DSM-V criteria (ICTRP)

non disponible

Critères d'évaluation principaux et secondaires
Part I: Changes from baseline in best acoustic speech variables to detect changes of dopaminergic and stimulation motor effect in Parkinson's disease patients;Part II: Changes from baseline in best acoustic and linguistic speech variables to detect changes of dopaminergic and stimulation neuropsychological effect in Parkinson's disease patients;Part III: Changes from baseline in best acoustic and linguistic speech variables to detect changes of dopaminergic and stimulation cognitive effect in Parkinson's disease patients;Part III: Changes from baseline in best acoustic and linguistic speech variables to detect changes of dopaminergic and stimulation cognitive effect in Parkinson's disease patients (ICTRP)

Dyskinesia severity;Momentary mood state;Momentary anxiety state;Bradyphrenia assessment (ICTRP)

Date d'enregistrement
non disponible

Inclusion du premier participant
non disponible

Sponsors secondaires
Czech Technical University in Prague (ICTRP)

Contacts supplémentaires
Paul Krack, Prof.Paul Krack, Prof.Paul Krack, Prof., paul.krack@insel.chpaul.krack@insel.ch, 31 66 4 03 7131 66 4 03 71, Insel Gruppe AG, University Hospital Bern (ICTRP)

ID secondaires
2022-01304 (ICTRP)

Résultats-Données individuelles des participants
non disponible

Informations complémentaires sur l'essai
https://clinicaltrials.gov/ct2/show/NCT05765110 (ICTRP)

Résultats de l'essai

Résumé des résultats

non disponible

Lien vers les résultats dans le registre primaire

non disponible