Training with surprise slips may teach stroke survivors to prevent falls
NCT ID NCT03205527
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This trial tests whether a special training that uses unexpected slips on a low-friction platform can help stroke survivors improve their balance and reduce falls. Participants will practice recovering from slips in a safe lab setting, and researchers will track whether these skills carry over to everyday life. The goal is to develop a simple, effective way to lower fall risk and improve walking function in people who have had a stroke.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Overground slip perturbation training
- What this could lead to
- If it works, this training could become a standard therapy to help stroke survivors prevent falls and regain safer walking.
- What could go wrong
- This is a small, early-stage study. The training may not translate to real-world falls, and results may not apply to all stroke survivors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
91 people
The number who actually took part.
- Started
-
Apr 2017
- Expected to finish
-
Mar 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
21 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects will have to be ambulatory (with or without assistive device) with self-reported chronic (\> 6 months) stroke-induced hemiparesis confirmed by participants' physician and medically cleared. Evidence of unilateral brain lesion confirmed by an imaging study (e.g. CT or MRI). * Subjects with no other acute and significant neurological, cardiopulmonary, musculoskeletal or systemic diagnosis or have undergone a recent major surgery (\<6 months) or hospitalization (\<3 months) and not on any sedative drugs * Ability to walk at least 10m with or without assistive device which includes use of ankle orthosis or functional electrical stimulation devices (which is equivalent to having a score of\> 4, dependent supervision on Functional Ambulatory category scale) Exclusion Criteria: * Severe osteoporosis (Ultrasound score \< -2) * Cognitive impairment (Mini Mental State Exam score\<25) * Aphasia (\<71% on Mississippi Aphasia Screening Test) * Severe depression ( \> 15 on Geriatric Depression Scale) * Severe obesity (BMI \>35Kilogram/m2) * Complains of shortness of breath, or uncontrolled pain (\> 3/10 on VAS), or if pulse oxygen drops \<92% on the 6 minute walk test (for endurance) * Uncontrolled hypertension (resting systolic blood pressure \> 165 mmHg and/or diastolic blood pressure \> 110mmHg) * Resting heart rate \> 85% of age-predicted maximal heart rate * Resting oxygen saturation \<95%
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Stroke are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Illinois at Chicago
Chicago, Illinois, 60612, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Effects of transcranial direct current stimulation and pelvic proprioceptive neuromuscular facilitation on trunk control, balance and functional mobility in stroke patients
- Correlation of visual and motor deficits in stroke patients
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
- Can a PET tracer reveal hidden brain inflammation?