Study on the treatment of hand dysfunction after cerebral apoplexy by brain regulation and training techniques combined with TCM acupuncture

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2022000036

Enrollment

Unknown

Registered

2022-06-24

Start date

2022-07-21

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Stroke

Interventions

experimental group:repetitive transcranial magnetic stimulation+scalp acupuncture+Hand robot

control group:False repetitive transcranial magnetic stimulation+False scalp acupuncture

Eligibility

Sex/Gender

All

Age

30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of cerebral infarction and cerebral hemorrhage; 2. Between 30 and 70 years old; 3. The first onset, the course of disease is between 2 weeks and 6 months after stroke, the condition is stable, can tolerate acupuncture and rehabilitation training treatment; 4. The patient had upper limb and hand dysfunction caused by stroke; 5. Patients who voluntarily participated in the clinical trial and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Hemiplegia patients caused by non-cerebrovascular diseases such as brain trauma, brain tumor and craniocerebral surgery; 2. Patients with cerebral infarction complicated with cerebral hemorrhage; 3. Patients with severe heart, lung, liver, kidney and other organ failure; 4. Patients with severe aphasia, severe hearing, understanding and cognitive dysfunction and unable to communicate; 5. Patients with a previous history of stroke and/or residual limb dysfunction; 6. In addition to stroke, there are other factors causing upper limb paralysis, such as Guillain-Barre syndrome, multiple sclerosis, myasthenia gravis, etc. 7. Poor compliance, not according to the doctor's advice for treatment; 8. Those who have received systematic rehabilitation treatment in the past; 9. Patients with epileptic history or eeg examination showing epileptic changes or intracranial metal and other foreign bodies.

Design outcomes

Primary

Measure	Time frame
FNIRS resting state/task state acquisition;	—

Secondary

Measure	Time frame
FMAS upper limb motor function assessment;Barthel index evaluation;Action evoked potentials (MEPs) were measured;	—

Contacts

Public ContactYuanbin Yang

Wangjing Hospital, China Academy of Chinese Medical Sciences

duyiran0506@126.com18210897538

Outcome results

None listed

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