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The Effect of iTBS Combined with Acoustic Startle Priming Motor Training on Upper Limb Motor Function and Neural Plasticity in Stroke Individuals

The Effect of iTBS Combined with Acoustic Startle Priming Motor Training on Upper Limb Motor Function and Neural Plasticity in Stroke Individuals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085220
Enrollment
Unknown
Registered
2024-06-03
Start date
2024-06-15
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Stroke

Interventions

iTBS+startle group:Transcranial magnetic stimulation + Acoustic Startle Priming Motor Training
iTBS+non-startle group:Transcranial magnetic stimulation+ Normal Priming Training
sham iTBS+startle group:sham iTBS + Acoustic Startle Priming Motor Training

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1)Age between 18 and 70 years, with both males and females eligible. (2)Onset of the first stroke within the past 3 months, with clear clinical symptoms and radiological diagnosis. (3)Severe upper limb motor impairment, with a Fugl-Meyer Assessment-Upper Extremity (FMA-UE) score between 0 and 35. (4)Stable vital signs for at least 48 hours. (5)Cognitive capacity to follow instructions, with a Mini-Mental State Examination (MMSE) score of >= 22. (6)Tolerance to sudden auditory startling stimuli of 114 decibels. (7)Willingness to provide informed consent.

Exclusion criteria

Exclusion criteria: (1)A history of strokes. (2)Severe upper/lower limb spasticity, with a Modified Ashworth Scale (MAS) grade of 3 or higher, or other conditions affecting upper and lower limb function, such as joint muscle contractures, severe frozen shoulder, fractures, arthritis, local skin ulcers, pressure sores, recent surgical incisions, etc; (3)Severe cognitive impairment, inability to effectively communicate with medical personnel; (4)Other conditions deemed unsuitable for participation by the researcher, such as severe hypertension, coronary heart disease, claustrophobia, etc.

Design outcomes

Primary

MeasureTime frame
Fugel-Myer motor Assessment for upper extremity, FMA-UE;modified Ashworth scale, MAS;

Secondary

MeasureTime frame
MEP;rest-state function MRI;diffusion tensor image;Quality of life;Retention rate;Adherence;Tolerability;Safety;

Countries

China

Contacts

Public ContactJing Zhang

Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

hbclleo@163.com+86 181 6407 3997

Outcome results

None listed

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