Skip to content

Study on the effect of preconditioning of Intermittent Theta Burst Stimulation with transcranial direct current stimulation based on fNIRS technology on post-stroke cognitive impairment

Study on the effect of preconditioning of Intermittent Theta Burst Stimulation with transcranial direct current stimulation based on fNIRS technology on post-stroke cognitive impairment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088086
Enrollment
Unknown
Registered
2024-08-12
Start date
2024-08-12
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

post-stroke cognitive impairment

Interventions

preconditioning of iTBS group:Administer pre regulated transcranial direct current stimulation (tDCS) to the cathode, followed by iTBS stimulation and cognitive rehabilitation training.
iTBS group:Provide false cathode tDCS stimulation pre regulation+iTBS+cognitive rehabilitation training
Control group:Provide false cathode tDCS pre regulation+iTBS false stimulation+cognitive rehabilitation training

Sponsors

Xuzhou Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) The diagnosis meets the diagnostic criteria for post-stroke cognitive impairment (PSCI) as outlined in the "Expert Consensus on Post Stroke Cognitive Impairment Management 2021" published by the Chinese Stroke Association and the Expert Committee on Post Stroke Cognitive Impairment Management in 2021. The MoCA score is less than 26 points and = 6 points; (2) Age range: 40-75 years old, all underwent head CT and MRI examinations; (3) Having sufficient visual and auditory resolution to undergo neuropsychological testing and other assessments; (4) First onset, within 6 months after stroke, with stable vital signs; (5) Right handed (6) subjects and/or guardians provide informed consent and sign a consent form, which has been approved by the Ethics Committee of Xuzhou Rehabilitation Hospital.

Exclusion criteria

Exclusion criteria: (1) Patients with cognitive impairment caused by various reasons other than stroke; (2) Severe dysfunction of important organs such as the heart, liver, kidneys, and lungs; (3) Patients with acute massive cerebral infarction or unabsorbed cerebral hemorrhage; (4) History of alcohol or drug abuse or dependence within the past 2 years; (5) Researchers believe that subjects who cannot follow the research procedure to complete the experiment; (6) Intracranial metal implants, magnetic plates, pacemakers, or skull defects; (7) Personal or family history of epilepsy, psychiatric history; (8) Patients with combined intracranial infection or open wounds or inflammation in the local skin of the treatment site; (9) Malignant tumors and pregnant women.

Design outcomes

Primary

MeasureTime frame
Loewenstein Occupational Therapy Cognitive Assessment(LOTCA);

Secondary

MeasureTime frame
Montreal Cognitive Assessment(MoCA);Oxyhemoglobin and deoxyhemoglobin concentrations;Relative power ratio of frequency band;Event related potential -P300 latency and amplitude;

Countries

China

Contacts

Public ContactShiyan Wang

Xuzhou Rehabilitation Hospital;Xuzhou Central Hospital

wangshiyan3669@163.com+86 181 1200 7636

Outcome results

None listed

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