Influence of supportive forces on daily activities
Zusammenfassung der Studie
This study is a cross-sectional study examining the influence of the supportive forces of the therapeutic robot FLOAT on the execution of daily activities. The study takes place at the Balgrist University Hospital in Zurich over a period of about 3 years. Measurements will be conducted on approximately 120 healthy subjects and 20 patients with an incomplete spinal cord injury. Study participants will be invited for a visit lasting about 140 minutes at the Balgrist University Hospital. During the visit, participants will repeatedly perform different daily activities (free walking, standing/sitting, stair climbing, and balancing) with and without supportive forces provided by the FLOAT. Their movements and muscle activities will be measured, allowing us to make statements about the naturalness of the movements. The collected data will also allow us to compare different movement patterns and draw conclusions about optimal support. This will enable future therapy of these daily movements to be specifically tailored to the patients and to train the movements with the help of the FLOAT under optimal conditions.
(BASEC)
Untersuchte Intervention
- Device: The cable robot FLOAT is a novel weight relief system that allows users to move freely in space. Users are connected to the robot via a harness. This allows the robot to exert three-dimensional forces on the users. The generated forces can be used to facilitate or disrupt a user's movements. Additionally, the FLOAT functions as a safety mechanism that detects and cushions any falls. The FLOAT can be used extremely versatile and its unique design allows therapies that have not been trainable with other robotic devices until now. - Application: This study will investigate how study participants manage various daily movements such as standing/sitting or stair climbing with and without the help of supportive forces from the therapeutic robot FLOAT. To this end, subjects will perform these daily movements and will be supported by forces of varying strengths and orientations.
(BASEC)
Untersuchte Krankheit(en)
Neurologically induced gait disorders in patients with an incomplete spinal cord injury (classified as AIS C-D according to the ASIA Impairment Scale)
(BASEC)
- Patients with incomplete spinal cord injury (AIS C-D) - Healthy volunteers without gait disorders - older than 18 years (BASEC)
Ausschlusskriterien
- Notable psychiatric or orthopedic (disorder of the human Musculoskeletal system) diagnosis - Notable secondary (in addition to spinal cord injury) neurological disorders - contraindications (circumstances that are against use of a Treatment / application talk) for FLOAT training (BASEC)
Studienstandort
Zürich
(BASEC)
Sponsor
Spinal Cord Injury Centre, University Hospital Balgrist Forchstrasse 340, CH-8008 Zurich
(BASEC)
Kontakt für weitere Auskünfte zur Studie
Kontaktperson Schweiz
Marc Bolliger
Tel. +41 44 510 72 01
marc.bolliger@clutterbalgrist.chUniversity of Zurich Spinal Cord Injury Center, Research Balgrist University Hospital Forchstrasse 340, 8008 Zurich
(BASEC)
Wissenschaftliche Auskünfte
nicht verfügbar
Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)
Ethikkommission Zürich
(BASEC)
Datum der Bewilligung durch die Ethikkommission
14.12.2016
(BASEC)
ICTRP Studien-ID
NCT03004144 (ICTRP)
Offizieller Titel (Genehmigt von der Ethikkommission)
Impact of robotic assistive forces on the performance of activities of daily living (BASEC)
Wissenschaftlicher Titel
Impact of Robotic Assistive Forces on the Performance of Activities of Daily Living (ICTRP)
Öffentlicher Titel
Impact of Assistive Forces on Activities of Daily Living (ICTRP)
Untersuchte Krankheit(en)
Spinal Cord Injury (ICTRP)
Untersuchte Intervention
Other: FLOAT (ICTRP)
Studientyp
Interventional (ICTRP)
Studiendesign
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Basic Science. Masking: None (Open Label). (ICTRP)
Ein-/Ausschlusskriterien
Gender: All
Maximum age: N/A
Minimum age: 18 Years
Inclusion Criteria:
- Individuals with incomplete spinal cord injury (AIS C-D) or able bodied persons
- informed consent as documented by signature
- bodyweight < 120 kg
Exclusion Criteria:
- a significant psychiatric or orthopedic diagnose
- any secondary neurological complications that may impact the outcome variables
- dermatological conditions (pressure ulcers, etc.)
- pacemaker or other implanted, electronic devices
- contraindications for FLOAT training
- inability or unwillingness to provide written informed consent or follow study
procedures e.g. due to language problems
- psychological disorders, dementia, etc.
- known or suspected non-compliance, drug or alcohol abuse
- enrolment of the investigator, his/her family members, employees and other dependent
persons (ICTRP)
nicht verfügbar
Primäre und sekundäre Endpunkte
3-dimensional kinematic analyses resulting in a detailed movement profile for each of the performed tasks (ICTRP)
nicht verfügbar
Registrierungsdatum
nicht verfügbar
Einschluss des ersten Teilnehmers
nicht verfügbar
Sekundäre Sponsoren
nicht verfügbar
Weitere Kontakte
nicht verfügbar
Sekundäre IDs
2016-01093 (ICTRP)
Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar
Weitere Informationen zur Studie
https://clinicaltrials.gov/ct2/show/NCT03004144 (ICTRP)
Ergebnisse der Studie
Zusammenfassung der Ergebnisse
2016-01093-studieenbericht.pdfLink zu den Ergebnissen im Primärregister
nicht verfügbar