WIM Exosuit Wearable Soft Robot for Enhancing Walking Activity

ConditionsStrokeHealthy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-89
SponsorShirley Ryan AbilityLab

About this trial

This study is to develop, test, and optimize a soft hip wearable robot for individuals who have experience a stroke.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

- Be at least 6 months post-stroke, have a diagnosis of Parkinson's, have a diagnosis of multiple sclerosis, or an adult older than 65 with no known neurological diagnoses.

Age: 18-89 years of age

For stroke, Parkinson's, multiple sclerosis, or older adult participants, must have adequate cognitive function (MMSE score >17)

Ability to walk at least 10 meters with maximum of 1 person assist

Disqualifiers

- <90 days post major orthopedic surgery (i.e. hip, knee, and/or ankle joint replacement.)

< 6 months post CABG or cardiac valve procedure

Any skin irritations / conditions that may preclude a participant from tolerating the use of the exosuit.

Severe osteoporosis, defined as osteoporosis that has been diagnosed and a participant's doctor has recommended pharmacologic treatment, or there is both a history of osteoporosis and a history of fractures.

Trial design

Design model

Single group

Treatments tested in this trial

  • WIM Robotic Exoskeleton

    Device

    Wearable hip-powered exoskeleton

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Healthy PopulationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

6-minute walk test

Primary outcome for Optimization aim of study.

Time frame
Baseline (Single-session)
2

Metabolic Cost

Primary outcome for Optimization aim of study. Data collected using Cosmed K5 Metabolic Unit

Time frame
Baseline (single session)

Secondary outcomes

Other outcomes

Sponsors and contacts

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