NCT05076565Active, not recruiting
Wearable Airbag Technology to Mitigate Falls in Individuals With High Fall Risk
Source: ClinicalTrials.gov · Last updated 29 Dec 2025
Brief summary (registry, in English)
The purpose of this study is to evaluate the feasibility and efficacy of a smart airbag system that detects and mitigates fall-related impact in individuals with high fall risk.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- First submitted
- 11 Jun 2021
- Start date
- 14 Jan 2018
- Primary completion date
- 14 Dec 2026
- Lead sponsor
- Shirley Ryan AbilityLab
- Diseases
- Stroke, Parkinson disease
- NCT number
- NCT05076565
What you commit to
- Study type: Interventional
- Planned participants: 200
- From 14 Jan 2018 to the primary completion date, 14 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Individuals currently on anti-coagulants.
Other illness
- Serious cardiac conditions, any musculoskeletal disorder, or other comorbidities that would interfere with participation in this minimal risk study.
- Non-healing ulcers of a lower extremity, Renal dialysis or end-stage liver disease, Legal blindness or severe visual impairment, a history of significant psychiatric illness.
Other
- Subjects reporting a head injury from exposure to a blast/concussion injury with one or more of the following symptoms: dizziness, vertigo, headache, migraine, oscillopsia, movement induced vertigo, imbalance.
- Individuals who use a wheelchair for mobility both outdoors and indoors.
- Waist circumference greater than 125 cm
- Non-English speaking individuals
- Severe Osteoporosis (status determined by self-reporting,medical records)
- The subject is pregnant, nursing or planning a pregnancy.
- Cognitive deficits or visual impairments (MMSE score \< 17) that would impair their ability to give informed consent or impair their ability to follow simple instructions during the experiments
Who the study is looking for
- Healthy, able-bodied subject
- Age constrained from 18-70 years old
- No injury to either upper or lower extremity or history of back pain
- English speaking.
- Exlusion Criteria - Able bodied Subjects:
- Waist circumference greater than 125 cm
- Pregnant women (status determined by self-reporting)
- Co-morbidity that interferes with the study (e.g. significant arthritis or joint problems, history of back injury, neuromuscular disorders, stroke, epilepsy, etc.)
- Individuals currently on anti-coagulants.
- Inactive, physically unfit
- Severe Osteoporosis (status determined by self-reporting)
- Non-English speaking
- Cognitive deficits or visual impairments (MMSE score \<17) that would impair their ability to give informed consent or impair their ability to follow simple instructions during the experiments
- Ages between 18-85 years old
- Individuals diagnosed with a Stroke (\> 6 months post), Parkinson's disease, aging elderly (ages 60-85)or lower-limb amputee with at least one self-reported fall in the last six months.
- Able to sit unsupported, walk at least with an assistive device and be able to follow a three-step command.
- For individuals with Parkinson's disease, Scoring 1 or higher on questions in Section II (Activities of Daily Living) and Section III (Motor examinations) on the Unified PD Rating Scale (UPDRS), be able to walk at least with an assistive device and be able to follow a three-step command.
- Waist circumference between 90 and 125 cm
- Either homebound or community ambulators.
- Willing to carry and use a smartphone and Airbag device.
- Willing to wear the airbag system as directed by the research personnel.
- English speaking
- Able and willing to give written consent and comply with study procedures.
Criteria the registry did not label
- INCLUSION AND EXCLUSION CRITERIA
- All potential subjects will be evaluated by research staff in order to match them to the inclusion and exclusion criteria that has been established - see below:
Age in the registry: 18 years to 85 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Shirley Ryan AbilityLab Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.