Pilot study on the feasibility of capturing therapies and effort during rehabilitation
Descrizione riassuntiva dello studio
In this study, we want to investigate whether it is possible to better document rehabilitation sessions using wearable sensors as well as audio and video recordings. During your regular therapy, you will wear two small sensors on your wrist. These measure, for example, your heart rate and your movement. Additionally, the therapy session will be recorded with a fixed camera to make your movements visible. The voice of the therapist will be recorded so that the content of the session can be reviewed later. Your own voice does not need to be recorded. Before starting therapy and after the end of therapy, you will sit quietly for five minutes each time to measure comparison values. After individual exercises, you will be briefly asked how strenuous the exercise was for you. Your therapy itself will not be changed by the study. No additional treatments will be performed. The study is only intended to check whether this type of data collection works well in regular therapy practice. Participation is voluntary. If you do not wish to participate or decide to withdraw later, it will not affect your treatment. All data will be treated confidentially and stored without your name.
(BASEC)
Intervento studiato
Non-invasive data collection during regular neurorehabilitation using two CE-marked wrist sensors to measure heart rate and movement, as well as a therapist-controlled audio recording and a fixed video recording of the therapy session to document the course of therapy.
(BASEC)
Malattie studiate
Neurological disorders with motor impairments (e.g., stroke, cerebral palsy, Parkinson's disease, amyotrophic lateral sclerosis)
(BASEC)
Inclusion criteria: Age ≥ 18 years Clinical diagnosis of a neurological disorder with motor impairment (e.g., stroke, cerebral palsy, Parkinson's disease, amyotrophic lateral sclerosis) Ability to participate in a therapy session of at least 30 minutes duration (BASEC)
Criteri di esclusione
Exclusion criteria: Acute infection or unstable medical condition Severe cognitive or communicative impairment that prevents consent or participation Skin diseases or skin changes that do not allow the attachment of sensors Implanted heart devices (e.g., pacemakers) that could interfere with measurement using the sensors (BASEC)
Luogo dello studio
Zurigo
(BASEC)
Sponsor
ETH Zurich
(BASEC)
Contatto per ulteriori informazioni sullo studio
Persona di contatto in Svizzera
Dr. Diego Paez-Granados
Tel. 078 713 16 84
diego.paez@clutterhest.ethz.chETH Zurich, SCAI-Lab, D-HEST Swiss Paraplegic Research (SPF)
(BASEC)
Informazioni scientifiche
non disponibile
Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)
Commissione etica Zurigo
(BASEC)
Data di approvazione del comitato etico
05.05.2026
(BASEC)
ID di studio ICTRP
non disponibile
Titolo ufficiale (approvato dal comitato etico)
Pilot Feasibility Study of Rehabilitation Therapy Content and Effort Logging (BASEC)
Titolo accademico
non disponibile
Titolo pubblico
non disponibile
Malattie studiate
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Intervento studiato
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Tipo di studio
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Disegno dello studio
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Criteri di inclusione/esclusione
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non disponibile
Endpoint primari e secondari
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non disponibile
Data di registrazione
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Inclusione del primo partecipante
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Sponsor secondari
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Contatti aggiuntivi
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ID secondari
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Risultati-Dati individuali dei partecipanti
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Ulteriori informazioni sullo studio
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Risultati dello studio
Riepilogo dei risultati
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Link ai risultati nel registro primario
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