NCT06708065Completed
Effects of Armeo Power Robot Therapy on Upper Limb Recovery in Hemiplegic Stroke Patients
Outcomes of Combining Armeo Power Robotic Therapy with Conventional Rehabilitation for Upper Limb Motor Recovery in Patients with Hemiplegia Following Supratentorial Cerebral Infarction
Source: ClinicalTrials.gov · Last updated 27 Nov 2024
Brief summary (registry, in English)
This study investigates the effectiveness of combining Armeo Power robotic therapy with conventional rehabilitation techniques to improve upper limb motor function in patients with hemiplegia caused by supratentorial cerebral infarction (a type of stroke). The study aims to evaluate how robotic-assisted therapy can enhance recovery by measuring motor function improvements over three weeks of treatment. Participants will undergo standard physical and occupational therapy alongside Armeo Power training, with results compared to those receiving only standard rehabilitation. The findings aim to provide valuable insights into advanced therapeutic options for stroke rehabilitation.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 84 (actual)
- First submitted
- 24 Nov 2024
- Start date
- 1 Jul 2023
- Primary completion date
- 30 Jun 2024
- Lead sponsor
- Hanoi Medical University
- Diseases
- Stroke
- NCT number
- NCT06708065
What you commit to
- Study type: Interventional
- Participants enrolled: 84
- From 1 Jul 2023 to the primary completion date, 30 Jun 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Severe sensory impairment in the affected limb.
- Hemiplegia caused by conditions other than stroke.
- Pre-existing motor disabilities in the affected limb before the stroke.
- Uncontrolled epilepsy.
Other
- Spasticity with a Modified Ashworth Scale score ≥ 3.
- Patients with arthritis or joint stiffness.
- Skin lesions on the limb requiring rehabilitation.
Who the study is looking for
- Spasticity of the affected arm with a Modified Ashworth Scale score ≤ 2.
- Patients must have good cognition and awareness (MoCA score ≥ 26).
- Patients must have good vision and visual perception.
- Patients must have stable sitting posture and good sitting balance.
- Body weight and affected arm size must be compatible with the robotic arm device.
- Patients must agree to participate in the study and adhere to the training protocol.
Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| 108 Military Central Hospital Coordinator of this site? Confirm its status | Hanoi | Vietnam | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.