Pilot study on the feasibility of capturing therapies and effort during rehabilitation
Zusammenfassung der Studie
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)
Untersuchte Intervention
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)
Untersuchte Krankheit(en)
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)
Ausschlusskriterien
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)
Studienstandort
Zürich
(BASEC)
Sponsor
ETH Zurich
(BASEC)
Kontakt für weitere Auskünfte zur Studie
Kontaktperson Schweiz
Dr. Diego Paez-Granados
Tel. 078 713 16 84
diego.paez@clutterhest.ethz.chETH Zurich, SCAI-Lab, D-HEST Swiss Paraplegic Research (SPF)
(BASEC)
Wissenschaftliche Auskünfte
nicht verfügbar
Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)
Ethikkommission Zürich
(BASEC)
Datum der Bewilligung durch die Ethikkommission
05.05.2026
(BASEC)
ICTRP Studien-ID
nicht verfügbar
Offizieller Titel (Genehmigt von der Ethikkommission)
Pilot Feasibility Study of Rehabilitation Therapy Content and Effort Logging (BASEC)
Wissenschaftlicher Titel
nicht verfügbar
Öffentlicher Titel
nicht verfügbar
Untersuchte Krankheit(en)
nicht verfügbar
Untersuchte Intervention
nicht verfügbar
Studientyp
nicht verfügbar
Studiendesign
nicht verfügbar
Ein-/Ausschlusskriterien
nicht verfügbar
nicht verfügbar
Primäre und sekundäre Endpunkte
nicht verfügbar
nicht verfügbar
Registrierungsdatum
nicht verfügbar
Einschluss des ersten Teilnehmers
nicht verfügbar
Sekundäre Sponsoren
nicht verfügbar
Weitere Kontakte
nicht verfügbar
Sekundäre IDs
nicht verfügbar
Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar
Weitere Informationen zur Studie
nicht verfügbar
Ergebnisse der Studie
Zusammenfassung der Ergebnisse
nicht verfügbar
Link zu den Ergebnissen im Primärregister
nicht verfügbar