Home hand training with a sensor egg for stroke, MS or Parkinson's
Tests a home sensor egg hand training program in adults with stroke, MS or Parkinson's.
Plain-language title generated from the registry record
Registry title: New Interactive Sensor-home-based Hand Training to Improve Dexterity
Key facts
- Where
- Lucerne, SwitzerlandSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 99 years old?
Source: NCT06062693, who can take part
Where in Switzerland
- Luzerner KantonsspitalLucerne, SwitzerlandTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Luzerner Kantonsspital
- Trial code
- NCT06062693
- Record updated
- 2 October 2023
- Original description
Primary objective of this study is to explore the impact of a 3-week upper limb hand function training in patients with PD, MS or stroke. The benefits on hand function of this training program will be evaluated. The hypothesize is that the 3-week upper limb hand function training improves finger dexterity.Read full original descriptionShow less
New Interactive Sensor-home-based Hand Training to Improve Dexterity
Primary objective of this study is to explore the impact of a 3-week upper limb hand function training in patients with PD, MS or stroke. The benefits on hand function of this training program will be evaluated. The hypothesize is that the 3-week upper limb hand function training improves finger dexterity.
Inclusion: Patients with confirmed PD, according to UK Brain bank Criteria (Hughes et al., 1992) or; MS patients with relapsing-remitting MS (RRMS), secondary-progressive MS (SPMS) or primary progressive MS (PPMS) according to the revised McDonald's criteria or; subacute stroke; written and signed informed consent; self-reported hand function problems; or; healthy subject; written and signed informed consent; no self-reported hand function problems.
Exclusion: psychiatric disease; Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc; MoCA <21/30; participation on other interventional trials.