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Clinical trial to investigate the effectiveness and safety of electroacupuncture and transcranial direct current stimulation combined with computerized cognitive rehabilitation for prevention of dementia

A randomized controlled trial to evaluate the effectiveness and safety of electro acupuncture and transcranial direct current stimulation with computerized cognitive rehabilitation in patients with vascular cognitive impairment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003644
Enrollment
45
Registered
2019-03-20
Start date
2019-04-04
Completion date
Unknown
Last updated
2021-01-06

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

Conditions

None listed

Interventions

Medical Device : Participants (n=45) are randomly assigned to Computerized cognitive rehabilitation treatment group (n=15), combination therapy of electroacupuncture and computerized cognitive rehabil

Sponsors

Chonnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged from 20 to 90years, 3months after stroke onset (verified by CT or MRI) and whose cognitive function is decreased 2) Korean version of the Montreal Cognitive Assessment (MoCA-K) score is below 22 3) Without blindness and able to communicate 4) No difficulty in reading and understanding Korean 5) Who voluntarily signed an informed consent form for participation in research

Exclusion criteria

Exclusion criteria: 1) Cognitive function is impaired due to brain tumors, encephalitis or traumatic brain injury. 2) Who is decreased in cognitive function prior to the stroke. 3) Who has severe depression and psychiatric disorders that is difficult to adapt the treatment. 4) Who had changed their medications and other treatments that may affect cognitive impairment within the last 1 month 5) Contraindications to electrostimulation (1) Metal in head (except in oral cavity) - cochlear implants, electrode or stimulator, clips or coils for aneurysm, stents, bullet fragments, deep brain stimulator, vagus nerve stimulator, eyeball implant (2) Who has pacemaker, defibrillator, neurostimulator, drug pump, intracardiac injection line (3) Continuous convulsion symptoms (4) Who received craniectomy, or ventriculo peritoneal shunt (VP shunt) surgery (5) Who continuously complains of elevated intracranial pressure symptoms such as headache, vomiting or nausea and others 6) Contraindications to scalp acupuncture (1) Wound or inflammation on the treatment region of scalp (2) Who has a tendency not to be haemostatic due to abnormalities of blood clotting system, haemophilia or others (3) Who had experienced serious unusual response after acupuncture treatment 7) Who cannot perform cognitive rehabilitation due to serious internal disease 8) Who cannot complete computer program due to musculoskeletal impairment, degenerative muscular disorders such as Parkinson disease, Huntington disease or others 9) Pregnant woman 10) Woman with pregnancy period

Design outcomes

Primary

MeasureTime frame
Lowenstein Occupational Therapy Cognitive Assessment (LOTCA)

Secondary

MeasureTime frame
Cognitive therapy and brain training (RehaCom);Korean version of Modified Bathel Index (K-MBI);European Quality of Life Five Dimension (EQ-5D-3L)

Countries

Korea, Republic of

Contacts

Public ContactJin-Seon Lee

Chonnam National University Hospital

Outcome results

None listed

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