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Robot-assisted Training of the Upper Limb in Persons With Multiple Sclerosis: an Randomized Controlled Trial

Robot-assisted Training on the Upper Limb in Persons With MS: an RCT

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02257606
Enrollment
17
Registered
2014-10-06
Start date
2011-07-31
Completion date
2011-09-30
Last updated
2015-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Brief summary

With this randomised intervention study, the investigators want to investigate the training effect of an 8 week training regime, using a robot-assisted training system in persons with MS. Besides conventional therapy, study participants in the experimental group will train 3 times per week during 30 minutes, using the haptic master. Research questions focus on the effects of additional robot assisted training on range of motion, movement quality and clinical tests for the upper limb in persons with MS. Evaluation by means of questionnaires and clinical outcome measures occured at baseline, after 4 weeks, after 8 weeks and at 16 weeks of follow-

Interventions

OTHERI-TRAVLE training

Sponsors

Revalidatie & MS Centrum Overpelt
CollaboratorOTHER
Expertise Centre for digital Media
CollaboratorUNKNOWN
tUL
CollaboratorUNKNOWN
iMinds
CollaboratorINDUSTRY
Interreg
CollaboratorOTHER
Hasselt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with Multiple Sclerosis (McDonald criteria), upper limb dysfunction due to muscle weakness (Motricity Index \<80), age \> 18 years

Exclusion criteria

* MS relapse or glucocorticosteroid treatment in the last month before the start of the study, upper limb paralysis (Motricity Index \< 18), other sever limitations, influencing participation (cognitive, visual)

Design outcomes

Primary

MeasureTime frameDescription
Motricity index2.5 min (pre-post)Random motor activity
Fugl-Meyer30 min (pre-post)Assessment of recovery of motor function
Action Research arm test15-20 min (pre-post)Grasp, grip, pinch, gross movement
Motor Activity log45 min (pre-post)perceived activities of daily life
Jamar handgrip strength2.5 min (pre-post)Handgrip strength

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 16, 2026