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The Effect of Exoskeleton-Assisted Gait Training on the Biomechanical Characteristics of Lower Limb Burn Scars

The Effect of Exoskeleton-Assisted Gait Training on the Biomechanical Characteristics of Lower Limb Burn Scars

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124499
Enrollment
Unknown
Registered
2026-05-13
Start date
2023-08-01
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Burn

Interventions

Control group:Routine Rehabilitation Therapy+Standard Walking Ability Training
Experimental Group:Routine Rehabilitation Therapy+Exoskeleton-Assisted Gait Training

Sponsors

Guangdong Provincial Work Injury Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Bilateral lower-extremity burns with a burn area exceeding 20% of the total body surface area (TBSA); 2. Generally stable clinical condition; 3. Duration of illness between 2 and 12 months; 4. Residual wounds <= 1% TBSA, with no severe infection; 5. Ability to stand independently or with the aid of assistive orthoses; 6. Presence of gait impairment; 7. Conscious and alert patients capable of clearly expressing their views and willing to cooperate with the study; 8. Those who voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe functional impairment resulting from their medical condition; 2. Patients with bone metabolic disorders (e.g., diabetes, hyperthyroidism); 3. Patients with concurrent pathologies of the bones, muscles, joints, or other systems that are sufficient to interfere with exoskeleton-assisted gait training; 4. Lactating or pregnant women; 5. Patients with cardiac disease complicated by atrial fibrillation; 6. Patients with severely elevated blood pressure (> 180/120 mmHg) for whom exoskeleton-assisted gait training and rehabilitation therapy are deemed unsuitable; 7. Patients with severe primary diseases affecting the liver, kidneys, hematopoietic system, or endocrine system, as well as patients with psychiatric disorders; 8. Patients unable to comprehend or complete the entire experimental protocol.

Design outcomes

Primary

MeasureTime frame
Limit of Stability;The total length of the center of gravity's trajectory is greater with eyes closed.;The total length of the center of gravity's trajectory is greater with eyes open.;Elastic modulus;Shear wave speed;

Secondary

MeasureTime frame
Function Ambulation Categories;6 minute walking;

Countries

China

Contacts

Public ContactXiao Xiao

Guangdong Provincial Work Injury Rehabilitation Hospital

togochina@163.com+86 182 1120 5140

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026