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Feasibility of ROBERT-SAS in severely impaired stroke patients

Feasibility of ROBERT-SAS in severely impaired stroke patients - Feasibility of ROBERT-SAS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON50980
Enrollment
20
Registered
2021-04-19
Start date
2021-08-19
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Cebrovascular accident Stroke

Interventions

None listed

Sponsors

Revalidatiecentrum Het Roessingh
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Sub(acute) stroke • Above 18 years • Able to provide informed consent • Unilateral ischemic or haemorrhagic stroke • Hemiparetic lower extremity

Exclusion criteria

Exclusion criteria: • Premorbid disability of lower extremity • Progressive neurological diseases like, dementia or Parkinson • Severe cognitive impairment, unable to follow simple instructions and unable to understand Dutch. • Skin lesions at the hemiparetic leg • Contraindication for mobilization like lower limb fracture • Pacemaker • Pregnancy

Design outcomes

Primary

MeasureTime frame
The main outcome parameter the success rate of intention detection, expressed as the % of times the electrostimulation is reached across all repetitions.

Secondary

MeasureTime frame
Secondary outcome values are: position, force, FES amplitude, trajectory completion rate (per stage 1-3), timing and velocity parameters and muscle activity. From the position data the joint angles will be derived, the force is measured with a build in force sensor and the muscle activity with sEMG electrodes.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)