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Impact of Crutch Type on Gait and Functional Outcomes Post-knee Surgery

Impact of Crutch Type on Kinematics, Electromyography, Pain, and Comfort Following Knee Arthroplasty and Anterior Cruciate Ligament Reconstruction

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04258917
Enrollment
0
Registered
2020-02-06
Start date
2021-01-08
Completion date
2022-04-11
Last updated
2022-04-18

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

Conditions

Anterior Cruciate Ligament Reconstruction, Total Knee Arthroplasty

Keywords

crutches, gait, mobility, adult, knee replacement, ACL tear

Brief summary

Study withdrawn

Detailed description

Study withdrawn

Interventions

DEVICEStudy withdrawn

Study withdrawn

Sponsors

University of Lethbridge
CollaboratorOTHER
University of Calgary
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Subjects 45-75 years old planning to get their first total knee replacement * Subjects 18-45 years old planning to get their first anterior cruciate ligament reconstruction

Exclusion criteria

* Previous injury to shoulder, elbow, or wrist * Current pain in shoulder, elbow, or wrist * Inflammatory arthritis (i.e. rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis), * History of cerebral palsy, stroke, significant cognitive impairment, or significant visual impairment * Problems with the heart or lungs * Currently using a crutch or crutches, walker, or other gait aid * History of using a crutch or crutches for 4 or more weeks * Inability to communicate in English * Current smoker * Currently pregnant

Design outcomes

Primary

MeasureTime frame
Range of scapular downward rotationMeasured during gait assessment on post-operative day 4-12

Secondary

MeasureTime frameDescription
Bilateral upper extremity kinematicsMeasured during gait assessment on post-operative day 4-12Hip flexion/extension, knee flexion/extension, and ankle dorsiflexion/plantar flexion; measured through optical motion tracking software
Bilateral upper extremity electromyographic (EMG) activityMeasured during gait assessment on post-operative day 4-12
Upper extremity painMeasured at 3 time points: pre-operative, during gait assessment, and 4 weeks post-operativeMeasurements of pain at the shoulder, elbow, and wrist using an 11-point Numerical Rating Scale (0 = no pain, 10 = extreme pain)

Other

MeasureTime frameDescription
Weight-bearing lower extremity kinematicsMeasured during gait assessment on post-operative day 4-12Hip flexion/extension, knee flexion/extension, and ankle dorsiflexion/plantar flexion; measured through optical motion tracking software
Number of fallsMeasured at 4 weeks post-operation
Torso kinematicsMeasured during gait assessment on post-operative day 4-12Thoracic flexion/extension; measured through optical motion tracking software
Spatiotemporal parametersMeasured during gait assessment on post-operative day 4-12Gait velocity, crutch stride length, weight-bearing lower extremity stride length; measured through timing lights and computer software
Crutch comfortMeasured during gait assessment on post-operative day 4-12Measured through an 11-point Numerical Rating Scale for both crutch types (0 = extremely uncomfortable, 10 = extremely comfortable)

Outcome results

None listed

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