Skip to content

Stationary robot in stroke rehabilitation

The effectiveness of a stationary robot in the rehabilitation of sub-acute stroke patients: a pilot randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN50278774
Enrollment
60
Registered
2022-03-14
Start date
2022-03-20
Completion date
Unknown
Last updated
2022-03-28

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

Conditions

Stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

After the medical examination and meeting the inclusion criteria, patients will be randomly assigned by the attending physician to participate in the study to one of the following groups. Patients wil

Sponsors

Akademii Wychowania Fizycznego im. Jerzego Kukuczki w Katowicach
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Women and men over 18 years of age 2. First history of ischemic or hemorrhagic brain 3. The period min. 1 month after stroke 4. The patient's consent to participate in the study 5. Ability to understand and follow the therapist's instructions 6. Ability to walk independently on a distance of 10 meters (it is allowed to use supporting tools, such as a walking stick, a ball or a walking frame)

Exclusion criteria

Exclusion criteria: 1. Contraindications to exercises in the study 2. Subarachnoid hemorrhage 3. Neurological diseases other than stroke affecting body balance and quality of the gait 5. Body structure, articular stiffness and other dysfunctions that are contraindicators to therapy in a stationary gait rehabilitation robot (mainly: body weight over 95 kg, body height below 150 cm and over 199 cm, difference in the length of the lower limbs over 1.5 cm, spasticity over the 3rd degree in Ashworth scale, wounds on the body at fixation sites on stationary rehabilitation robot)

Design outcomes

Primary

MeasureTime frame
1. Gait assessed by 10 Metre Walk Test (10MWT), at baseline and after the 3-week rehabilitation period 2. Gait assessed by treadmill walking test (Zebris FDM-T; Rehawalk, MaxxusDaum h/p Cosmos Force) at baseline and after the 3-week rehabilitation period 3. Spatial and temporal gait parameters assessed using the 3D MyoMotion device (Noraxon, USA) at baseline and after the 3-week rehabilitation period

Secondary

MeasureTime frame
1. Static and dynamic body balance assessed by Berg Balance Scale (BBS) at baseline and after the 3-week rehabilitation period 2. Dynamic body balance assessed by Time Up and Go Test (TUG) at baseline and after the 3-week rehabilitation period 3. Dynamic body balance assessed by Functional Reach Test (FRT) at baseline and after the 3-week rehabilitation period 4. Static body balance assessed by stabilometric platform (Zebris FDM-T; Rehawalk, MaxxusDaum h/p Cosmos Force) at baseline and after the 3-week rehabilitation period 5. Quality of life assessed with Stroke Impact Scale (SIS - 59) at baseline and after the 3-week rehabilitation period 6. ADL assessed with Barthel Scale at baseline and after the 3-week rehabilitation period

Countries

Poland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026