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临床试验/NCT06747676
NCT06747676暂停1 期

Graviceptive Neglect After Stroke: Clinical, Neuroanatomical and Physiological Effects of Focal Neuromodulation

University of Sao Paulo2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2025年1月3日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
暂停
入组人数
28
试验地点
2
主要终点
Visual Verticality Perception (VV; visual graviceptive neglect)

研究概览

简要总结

We aim to determine if targeted high-definition transcranial direct current stimulation (HD-tDCS) can safely correct errors in visual verticality perception in patients after stroke affecting either hemisphere.

详细描述

This study explores a new approach to treat graviceptive neglect, a condition that affects balance and perception of uprightness, using a non-invasive brain stimulation technique called HD-tDCS (high-definition transcranial direct current stimulation). Using a phase I/II randomized sham-controlled double-blind parallel clinical trial design, we aim to analyze if HD-tDCS can safely help correct abnormal visual verticality perception in 28 people after stroke. We will also investigate the effects of our protocol on cerebrovascular response using transcranial Doppler and cortical activity using EEG. Neuroanatomical characteristics will be analyzed to establish the relationship between verticality perception error and the extent of temporo-parietal junction (TPJ) damage and, more broadly, the putative VV structural brain Network (VVN). Each participant will receive six HD-tDCS sessions of 2mA for 20 minutes in a central cathode montage applied over the contralesional TPJ. Patients will be randomized into two groups, with 50% receiving active stimulation and 50% receiving sham stimulation. The sham stimulation condition will consist of the same electrode placement, with a 2mA ramp-up over 30 seconds, followed by a 30-second ramp-down. Both groups will undergo 6 sessions, three times a day, for 2 days. The follow-up assessment will be performed 1 month after stimulation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

Statistician

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Supratentorial ischemic stroke diagnosed by neuroimaging and clinical analysis;
  • •Clinically stable (stable vital signs for 24 hours; no chest pain in the last 24 hours; no significant arrhythmia; no evidence of deep vein thrombosis);
  • •Normal or corrected-to-normal vision;
  • •No previous experience with HD-tDCS;
  • •Ability to provide informed consent (patient or legal representative);
  • •Ability to comply with the intervention and assessment schedule of the protocol.
  • •Presence of visual verticality misperception.

排除标准

  • •Migraine;
  • •Pregnancy;
  • •Pacemakers;
  • •Seizures;
  • •Claustrophobia;
  • •Transient ischemic attack;
  • •Other neurological disorders;
  • •Psychiatric disorders;
  • •Sensitive scalp or prior brain surgery;
  • •Diagnosis of severe carotid atherosclerotic disease (stenosis ≥ 70%);
  • •Presence of metal implants, cardiac pacemakers, or claustrophobia;
  • •Diagnosis of COVID-19 or other infectious disease that requires isolation;
  • •Uncontrolled medical problems, such as terminal cancer or kidney disease.
  • •Left-handed or mixed-handed individuals as determined using the Edinburgh Handedness Inventory (Appendix 10);
  • •Peripheral vestibular deficits observed using neuro-otological screening tests when the participant's clinical condition allows (head shake test, head thrust test, Dix-Hallpike, and Pagnini-McClure);
  • •Prior musculoskeletal disorders affecting alignment and postural balance (e.g., moderate to severe scoliosis; torticollis);
  • •Cognitive dysfunction outside normal limits on the Mini-Mental State Examination (score below 23);
  • •Global or Wernicke's aphasia;

研究组 & 干预措施

Sham HD-tDCS

Sham Comparator

Participants will receive six sessions of 2mA sham HD-tDCS cathode center over the contralesional TPJ for 20 minutes, 3 times daily for 2 days with session intervals greater than 3 hours.

干预措施: Sham: High-Definition transcranial Direct Current Stimulation (HD-tDCS) (Device)

Active HD-tDCS

Experimental

Participants will receive six sessions of 2mA active HD-tDCS cathode center over the contralesional TPJ for 20 minutes, 3 times daily for 2 days with session intervals greater than 3 hours.

干预措施: Active: High-Definition transcranial Direct Current Stimulation (HD-tDCS) (Device)

结局指标

主要结局

Visual Verticality Perception (VV; visual graviceptive neglect)

时间窗: From baseline (before the first session) to 1 day post-intervention protocol (after six HDtDCS sessions).

Change in VV: assessment using the bucket method.

次要结局

  • Spatial neglect(From baseline (before the first session) to 30±5 days post-intervention protocol (after six HDtDCS sessions).)
  • Visual Verticality Perception (VV; visual graviceptive neglect)(From baseline (before the first session) to 30±5 days post-intervention protocol (after six HDtDCS sessions).)
  • Ocular torsion(From baseline (before the first session) to 30±5 days post-intervention protocol (after six HDtDCS sessions).)
  • Electroencephalography(From baseline (before the first session) to 30±5 days post-intervention protocol (after six HDtDCS sessions).)
  • Cerebrovascular reactivity(From baseline (before the first session) to 30±5 days post-intervention protocol (after six HDtDCS sessions).)
  • Ocular torsion(From baseline (before the first session) to 1 day post-intervention protocol (after six HDtDCS sessions).)
  • Electroencephalography(From baseline (before the first session) to 1 day post-intervention protocol (after six HDtDCS sessions).)
  • Cerebrovascular reactivity(From baseline (before the first session) to 1 day post-intervention protocol (after six HDtDCS sessions).)
  • Spatial neglect(From baseline (before the first session) to 1 day post-intervention protocol (after six HDtDCS sessions).)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Taiza G. S. Edwards, PhD

PhD

University of Sao Paulo

研究点 (2)

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