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Observation on the therapeutic effect of transcutaneous acupoint electrical stimulation with meridian flow on stroke-related circadian dysrhythmia sleep-wake disorders

Observation on the therapeutic effect of transcutaneous acupoint electrical stimulation with meridian flow on stroke-related circadian dysrhythmia sleep-wake disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000311
Enrollment
Unknown
Registered
2024-08-27
Start date
2022-06-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Stroke related circadian rhythm disorder sleep wake disorder

Interventions

Drug group:On the basis of sleep hygiene education and behavioral management, the melatonin receptor agonist agomelatine was orally administered at a dose of 25 mg/d, while the medication group was gi
Meridian flow group:On the basis of sleep hygiene education and behavior management, the two groups were treated with melatonin receptor agonist(25mg/d), the Ziwu Liuzhu group was given meridian injec

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1)Meeting the diagnostic criteria for stroke and circadian rhythm disorder of sleep; (2)Aged between 35 and 70 years old without cognitive impairment and no cognitive dysfunction, able to fully understand the scale and cooperate with treatment; (3)Understanding and agreeing to join the study and signing a written informed consent form; (4)No allergic reactions to treatment drugs.

Exclusion criteria

Exclusion criteria: (1) Patients with severe hepatic and renal insufficiency; (2) People with severe cognitive and communication disabilities and those with visual and hearing disabilities; (3) Combined with serious mental illness and other sleep disorders; (4)the skin at the acupoint is damaged; (5)People who have taken sleeping pills or antidepressant anxiety drugs in the past; (6)Patients with peripheral nerve and muscle system disease; (7) Pregnancy, lactation, pregnancy preparation in the near future.

Design outcomes

Primary

MeasureTime frame
Sleep quality; Sleep efficiency \ wake times \ sleep latency \ total sleep time;

Secondary

MeasureTime frame
12.5%;HAMA score;HAMD score;

Countries

China

Contacts

Public ContactTian Jun

Zhongnan Hospital of Wuhan University

tianjun@znhospital.cn18995540980

Outcome results

None listed

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