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Anchor axillary crutches

Development and Evaluation of an Ergonomically Optimized Anchor-Based Axillary Crutch for Enhanced Ambulatory Stability and Energy Efficiency

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260703002
Enrollment
20
Registered
2026-07-03
Start date
2026-08-31
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Mobility limitation requiring axillary crutch-assisted ambulation Crutch-Assisted Gait

Interventions

Participants perform non-weight-bearing walking on a treadmill using a standard axillary crutch.,Participants perform non-weight-bearing walking on a treadmill using a Anchor axillary crutch.,Particip
Standard Axillary Crutch,Anchor Crutch,Ergonomic Anchor Crutch with Contoured Axillary Pad and Spring-Assisted Mechanism

Sponsors

Burapha University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Healthy adults aged 20 to 40 years 2. no history of musculoskeletal, neurological, or cardiovascular disorders 3. able to safely use axillary crutches after familiarization training 4. body Mass Index (BMI) between 18.5 and 25.0 kg 5. willing to participate and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. History of upper or lower extremity injury within the previous 6 months 2. presence of pain or discomfort during walking 3. inability to complete treadmill walking according to the study protocol 4. known allergy to EMG electrodes or skin adhesive materials 5. any medical condition that may interfere with safe participation

Design outcomes

Primary

MeasureTime frame
Physiological Cost Index (PCI) before, during and after the 15-minute walking test under each crutch condition. Physiological Cost Index calculated from heart rate and walking speed during treadmill-assisted non-weight-bearing gait using each crutch condition.

Secondary

MeasureTime frame
Muscle Activation (EMG) before, during and after the 15-minute walking test under each crutch condition. Surface electromyography (EMG) amplitude normalized to MVC (%MVC) of Triceps brachii, Latissimus dorsi, Vastus lateralis, Biceps femoris, Gastrocnemius medialis, and Tibialis anterior.,Muscle Oxygenation before, during and after the 15-minute walking test under each crutch condition. Local muscle oxygen saturation measured using near-infrared spectroscopy (NIRS Moxy Monitor) at Triceps brachii and Vastus lateralis.,Rate of Perceived Exertion (RPE) before and immediately after completion of each walking condition. Perceived exertion assessed using Borg Rating of Perceived Exertion Scale (6 to 20).,Trunk displacement before and during the 15-minute walking test under each crutch condition. A smartphone-based inertial sensor application will be attached to the trunk to measure trunk displacement and movement variability during non-weight-bearing treadmill walking.

Countries

Thailand

Contacts

Public ContactSIRIRAT KIATKULANUSORN

Burapha University, Thailand

siriratk@go.buu.ac.th0882302582

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026