Intervention Effect of Transcranial Alternating Current Stimulation (tACS) on Disorder of Consciousness (DOC)

Sponsor
Anhui Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06076733
Collaborator
(none)
40
1
2
24
1.7

Study Details

Study Description

Brief Summary

To investigate the effect of high definition-transcranial alternating current stimulation(HD-tACS) on consciousness promotion in patients with chronic consciousness disorders and the underlying neural mechanism by EEG.

Condition or Disease Intervention/Treatment Phase
  • Device: high definition-transcranial alternating current stimulation
  • Device: sham transcranial alternating current stimulation
N/A

Detailed Description

Forty patients with chronic consciousness disorder who met the inclusion criteria were recruited with the informed consent of the family. All the participants were randomized to receive "active" or "sham" treatment protocol. Stimulation was performed using a alternating stimulator linked to one anodal electrode and four cathodal electrodes. The anodal electrode was placed over the left dorsolateral prefrontal cortex (DLPFC; F3 in the 10-20 international system of EEG placement), and the four cathodal electrodes (AFz, FCz, F7, and C5 in the 10-20 international system EEG placement) were placed around the anodal electrode to form a current loop. Twenty 2 milliampere (mA) sessions (ramp-up and ramp-down periods of 30 and 30 seconds, respectively) were applied for 20 minutes per session, twice daily over 10 consecutive days, and the stimulus frequency was set as 6 Hertz (Hz). Sham tACS was delivered using the same protocol and current intensity, but the period of active stimulation was only during the ramp-up and ramp-down periods of 30 and 30 seconds. Before and after the tACS treatment, the state of consciousness was assessed according to coma recovery scale-revised(CRS-R), and19-channel EEG data were collected.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
To Explore the Intervention Effect of High Definition-transcranial Alternating Current Stimulation (HD-tACS) on Consciousness Promotion in Patients With Chronic Consciousness Disorders and the Potential Neural Mechanism
Actual Study Start Date :
Sep 21, 2023
Anticipated Primary Completion Date :
Sep 20, 2025
Anticipated Study Completion Date :
Sep 20, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: active group

Twenty 2-mA sessions (ramp-up and ramp-down periods of 30 and 30 seconds, respectively) were applied for 20 minutes per session, twice daily over 10 consecutive days, and the stimulus frequency was set as 6Hz.

Device: high definition-transcranial alternating current stimulation
tACS is described as a non-invasive form of brain stimulation that uses a low-intensity, alternating current applied directly to the head through scalp electrodes.

Sham Comparator: sham group

Sham tACS was delivered using the same protocol and current intensity, but the period of active stimulation was only during the ramp-up and ramp-down periods of 30 and 30 seconds.

Device: sham transcranial alternating current stimulation
Sham tACS was delivered using the same protocol and current intensity, but the period of active stimulation was only during the ramp-up and ramp-down periods of 30 and 30 seconds.

Outcome Measures

Primary Outcome Measures

  1. Assessment of Coma Recovery Scale [Before intervention and one day after all intervention]

    State of consciousness was assessed by two trained physicians in three different time periods using the Coma Recovery Scale-Revised (CRS-R), which has demonstrated good reliability and validity for the behavioral evaluation of disorder of consciousness (DOC) patients. Total score ranges from zero to twenty-three, with higher scores indicating better neurological function and prognosis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. patients diagnosed as chronic disorders of consciousness based on CRS-R assessment by at least two professional neurologists;

  2. the age requirement is between 18 and 75;

  3. vital signs need to be stable;

  4. no neuromuscular blockers and sedatives have been used within 24 hours before the study and the entire protocol;

  5. no improvement in the state of consciousness was observed within one week before the start of the study.

Exclusion Criteria:
  1. previous or current diagnosis of severe neurocognitive degenerative diseases;

  2. metal implantation in the head;

  3. previous surgical procedures resulted in skull defect;

  4. previous history of epilepsy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Anhui Medical University Hefei Anhui China

Sponsors and Collaborators

  • Anhui Medical University

Investigators

  • Principal Investigator: Kai Wang, PhD, Director of medical psychological department, Anhui Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
WANG KAI, Director of medical psychological department, Anhui Medical University, Anhui Medical University
ClinicalTrials.gov Identifier:
NCT06076733
Other Study ID Numbers:
  • AHMU-tACS-DOC
First Posted:
Oct 11, 2023
Last Update Posted:
Oct 12, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by WANG KAI, Director of medical psychological department, Anhui Medical University, Anhui Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 12, 2023