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Testing control settings of a wearable leg robot to help walking after stroke

Tests how a wearable leg robot is controlled in adults recovering from stroke.

Key facts

Who runs it
Eighth Affiliated Hospital, Sun Yat-sen University
Where
Shenzhen, ChinaSee the site
Trial code
Registry title
The Effects of the Control Strategies of Wearable Lower Limb Rehabilitation Robots
Status
Recruiting
People taking part
10 people, planned
Started
23 Oct 2024
Expected to end
22 Apr 2027
Type of study
Interventional
Treatments tested
  • Robot-assisted overground gait training
Record updated
26 June 2025

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 75 who had a stroke at least 3 months ago. They must be medically stable and able to walk 10 meters on their own.

Age
18 to 75 years
Sex
All sexes can join.
Disease stage
Stroke that happened at least 3 months ago, with weakened leg movement but some muscle activity left in the legs.
Earlier treatment
People currently receiving other rehabilitation or experimental treatments cannot join.

Main reasons for not taking part

  • Severe memory or thinking problems that prevent following the treatment plan
  • Severe balance or coordination problems
  • Other serious movement problems, such as abnormal muscle tone or ataxia
  • Active heart or blood vessel disease or other serious illness
  • Leg fractures, serious bone problems, or skin ulcers and infections

The registry criteria, word for word

Show all 15 criteriaShow less

Who can take part

  • Stroke patients aged between 18 and 75 years. Patients who are medically stable and able to stand and walk independently for at least 10 meters during rehabilitation
  • Stroke event occurred at least 3 months ago Patients with impaired lower limb motor function but with some degree of muscle activity in the lower extremities
  • Patients without severe cognitive impairment and capable of understanding and following the treatment protocol
  • Patients without severe balance or coordination disorders, able to maintain balance and perform gait training with assistive devices
  • Patients without lower limb fractures or other serious skeletal issues affecting the lower limbs
  • Patients without severe cardiovascular or other serious illnesses and able to tolerate the intensity and duration of rehabilitation therapy
  • Patients willing to participate in the study and able to provide written informed consent

Who cannot take part

  • Lower limb fractures or other serious skeletal issues that may impact the suitability and safety of robot-assisted rehabilitation therapy
  • Patients currently receiving other rehabilitation or experimental treatments. Patients with skin ulcers, infections, or other severe skin conditions that may interfere with the use and application of robotic devices
  • Unexplained discomfort or pain symptoms that may limit the patient's ability to participate in rehabilitation therapy
  • Severe cognitive impairment that prevents the patient from understanding or complying with the treatment protocol
  • Severe balance or coordination disorders that prevent the patient from maintaining balance and participating in gait training, even with assistive devices
  • Other serious motor disorders, such as abnormal muscle tone or ataxia, which may interfere with the effectiveness of rehabilitation therapy
  • Active cardiovascular disease or other serious systemic illnesses that may affect the patient's safety or treatment outcomes
  • Failure to meet other specific inclusion criteria outlined in the study protocol

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Where in China

  • Eight affiliated hospital, Sun Yat-Sen UniversityShenzhen, ChinaContact: Shaofeng ZhaoTaking people

About the trial

What the trial wants to find out

Post-stroke patients were required to complete a session of robot-assisted training, which involved nine repetitions of 5-meter overground walking (three trials for each of the three controllers) in a rectangular hospital corridor.

The group in the trial

  • Robot gait training groupTreatment being tested

    During this study, we will explore which control strategy: Aware Hip Knee Coupling Control (AHKC), Passive control (PC), or fixed compliance control (FCC) may be optimal for post-stroke subjects

    Treatment: Robot-assisted overground gait training

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Effects of Control Strategies in Wearable Lower Limb Rehabilitation Robots
Plain-language title
Testing control settings of a wearable leg robot to help walking after strokeGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT07037849, who can take part
Record updated
26 June 2025