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Evaluation of the Effectiveness and Safety of AI-Robotics

Prospective, Multicenter, Self Controlled Evaluation of the Effectiveness and Safety of Lower Limb Exoskeleton Rehabilitation Training Robot

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03452059
Acronym
ART
Enrollment
40
Registered
2018-03-02
Start date
2017-07-11
Completion date
2018-01-13
Last updated
2018-07-30

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

Conditions

Lower Extremity Motor Dysfunction, Spinal Cord Injury

Keywords

Paralysis, Lower Extremities, Ai-Robotics

Brief summary

Evaluation of the effectiveness and safety of the lower extremity exoskeleton rehabilitation training robot

Detailed description

Evaluation of the effectiveness and safety of the lower extremity exoskeleton rehabilitation training robot developed by AI-Robotics Technology Co., Ltd., Beijing for who had lower limb paralysis

Interventions

DEVICEAiLegs, AiWalker and HKAFO

5 days. Using their own control method, each morning using AiLegs, AiWalker AiWalker and HKAFO for 6 minutes walk test, three kinds of appliance between at least 30 minutes to determine heart rate, blood pressure and breathing back to quiet level. Repeat the same procedure in the afternoon ,the order is also random. Each participant will complete 10 groups of lower limb exoskeleton rehabilitation Training robot (including AiLegs, AiWalker two models) and HKAFO 6 minutes walking test

Sponsors

AI-Robotics Technology Co., Ltd
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. more than18 but less than 60 years old,less than 80 kilos of weight,Gender is not limited 2. Confirmed by MR/CT,AIS spinal cord injury grade: A-C level (without walking ability):Damage plane T6-L2 3. The muscle tension of the modified Ashworth grade level is less than or equal to 2 4. The range of passive motion of the hip and knee joint of the patient is approximately normal in the ankle joint Neutral position 5. Upper limb strength and physical strength are sufficient to stabilize the crutches 6. Patients are able to understand and actively participate in the training program, agree and sign the informed consent form

Exclusion criteria

1. The range of motion of the joints is severely limited and the walking action is limited 2. Spinal fractures are not completely healed, the clinical situation is unstable; if not fully confirmed,please go department of orthopedics or other clinical departments for diagnosing 3. Skin injury or infection of the lower extremities or the part of wearing robot 4. Unstable angina, severe arrhythmia and other heart diseases 5. Severe chronic obstructive pulmonary disease 6. Unilateral neglect 7. Severe cognitive or visual impairment 8. Other contraindications or complications that may affect walking training 9. Pregnant or lactating women 10. The investigators find that patients with poor compliance, unable to complete the study in accordance with the requirements

Design outcomes

Primary

MeasureTime frameDescription
Walking efficiency6 minute6 minute walk distance,measured by meters

Secondary

MeasureTime frameDescription
Cardiovascular responseduring 6 minute walk test and right before the 6MWTheart rate during and after 6 minute walk test
efficiency of put on or take off the Ailegs/Aiwalker/HKAFOimmediately before beginning (pre-) and immediately after finishing (post-) each of 6 minute walk testto measure the time of putting on or taking off the Ailegs/Aiwalker/HKAFO before or after 6 min walk test
RPE questionaireafter 6 minute walk testthe RPE is recorded after the 6 min walk test

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026