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iTBS combined with robotic-assisted gait training improves walking dysfunction after stroke: a randomized controlled study

iTBS combined with robotic-assisted gait training improves walking dysfunction after stroke: a randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087266
Enrollment
Unknown
Registered
2024-07-24
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Stroke

Interventions

1:combined iTBS and robotic assisted gait training
2:robotic assisted gait training

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University , Rehabilitation Campus
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients with hemiplegia in stroke who meet the diagnostic criteria for cerebral haemorrhage and cerebral infarction in the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Haemorrhage (2019) and the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke (2018), and whose diagnosis has been confirmed by CT or MRI examination; (2) Age of 30 to 75 years old, gender is not limited; (3) The first onset of the disease, the duration of the disease is 1-6 months after stroke; (4) Patients with lower limb modified Ashworth classification = grade 2 and Brunnstrom stage = stage 3; and (5) Able to walk 10m on foot with supervision or independently; (6) No visual or psychological impairment; (7) No severe cognitive problems (MMSE>20) and able to understand and follow instructions; (8) Stable condition and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Those with severe cognitive and speech disorders who are unable to co-operate with a training programme; (2) Those who are partially blind and have visual impairment; and (3) Those with vestibular dysfunction such as vertigo and tinnitus; (4) Those with serious bone and joint diseases, serious cardiopulmonary diseases who are unable to train; and (5) Those with deteriorating conditions; and (6) Wearing a pacemaker, having metal implants in the skull or body, or the presence of cranial bone defects, etc. that make it impossible to carry out TBS treatment.

Design outcomes

Primary

MeasureTime frame
3 Dimension gait analysis;Surface electromyography;Fugl-Meyer Assessment lower extremity ;Tinetti performance oriented mobility assessment, POMA;

Secondary

MeasureTime frame
Time up and go test;Functional ambulation category scale, FAC ;Functional comprehensive assessment, FCA;Functional Near Infrared Spectroscopy;Quantitative Electroencephalography;6 minute walking test;Motricity Index;

Countries

China

Contacts

Public ContactXuekang Niu

The Third Affiliated Hospital of Zhejiang Chinese Medical University

631271065@qq.com+86 188 0571 9518

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026