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The effect of gait assistance robot training on the scars in burn patients

The effect of gait assistance robot training on the biomechanical scar properties in burn patients: a randomized control trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005204
Enrollment
36
Registered
2020-07-07
Start date
2020-06-15
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

None listed

Interventions

Medical Device : -Robot training method- Gait training is carried out using the gait assisted rehabilitation robot SUBAR® (CRETEM Co. Ltd, Anyang-si, South Korea). Before starting the robot-assisted g
s lower extremity by measuring the length from the hip joint to the knee and knee to foot. As a next step, put the patient&#39
s both legs into the SUBAR® exoskeleton and secure the thighs and lower legs. Gait speed can be adjusted in 5 steps from 1 to 5 depending on the degree of gait disorder of the patient, and appropriate
s muscle strength and joint motion angle. Gait training was administered to the treatment group for 30 minutes once a day, once a day, 5 times a week, and 8 weeks in 3 ways: in situ walking, forward w

Sponsors

Hallym University Medical Center-Hangang
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients more than 19 years of age who have limited movement and gait disturbance due to burn scar contracture on both lower extremities

Exclusion criteria

Exclusion criteria: -Patients with physical conditions not suitable for robot wearing: weight >100 kg, height <150 cm or >185 cm -Patients with scar bleeding or scars with risk of epidermal damage when applying a robot -Patients with uncontrolled hypertension or orthostatic hypotension -Patients who have difficulty controlling the robot due to cognitive decline or impaired upper limbs -Patients with moderate to severe joint disease -Patients with contraindications to lower extremity weight load such as fractures

Design outcomes

Primary

MeasureTime frame
NRS, numeric rating scale;6 minutes gait test;active range of motion of joint;biomechanical scar properties-melanin, erythema, elasticity

Secondary

MeasureTime frame
thickness of scar using ultrasound device

Countries

Korea, Republic of

Contacts

Public ContactYoon Soo Cho

Hallym University Medical Center-Hangang

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 13, 2026