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Powered Assist Hip Exoskeleton to Improve Ambulation in Severe Lung Disease

Exoskeleton Assist to Improve Physical Performance in Patients With Very Severe Chronic Respiratory Disease

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05835271
Enrollment
12
Registered
2023-04-28
Start date
2023-08-01
Completion date
2027-09-30
Last updated
2026-08-20

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

Conditions

Lung Disease Chronic

Keywords

Walking, Exoskeleton Device

Brief summary

Chronic respiratory disease (CRD) is among the most prevalent and growing diseases worldwide with disabling consequences. Many with a compromised respiratory system cannot support the metabolic energy demands of walking causing them to walk slowly and stop often. Those with CRD could receive substantial benefit from a powered wearable exoskeleton device that assumes part of the energy of walking. Assisting the legs will lower the metabolic energy demands, and therefore the ventilation required for exercise, thereby allowing them to walk faster and further. Proposed is a series of single-case experiments comparing walking endurance with and without a powered hip exoskeleton assist. The aim of this study is to determine the efficacy of an exoskeleton on walking endurance in ventilatory limited patients with CRD. An exoskeleton could be a novel immediate and long term strategy to augment walking as part of the spectrum of pulmonary rehabilitation and community reintegration.

Interventions

A powered exoskeleton describes a wearable robot designed around the shape and function of the human body with segments and joints externally coupled to those of the user. The exoskeleton includes a rigid outer frame, sensors that detect a user's desired movements, a computerized controller, motors and actuators, and lightweight batteries. The exoskeleton is designed to be worn in the community.

Sponsors

West Park Healthcare Centre
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A prospective longitudinal, self-controlled, single-case repeated measures alternating treatment, randomized and counterbalanced cross-over experimental trial design, comparing walking endurance without and with a powered exoskeleton.

Eligibility

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

Inclusion criteria

* stable chronic respiratory disease * modified medical research council dyspnoea score (mMRC) ≥ 2

Exclusion criteria

* evidence of cardiac rhythm or circulatory compromise * myocardial infarct within the previous three months * moderate-severe aortic stenosis * uncontrolled hypertension * sustained cardiac arrhythmias * untreated neoplasia * lung surgery within the previous three months * any other predominant co-morbidities or treatments that might influence walk testing * body size outside of exoskeleton fit specifications * skin sores or skin breakdown in the area where the device is worn * a high risk of fracture

Design outcomes

Primary

MeasureTime frameDescription
walking endurance timean average of 7 tests over 4 weekstolerance (time) of an individualized constant, brisk, walking speed endurance test

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORRoger Goldstein

West Park Healthcare Centre

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026