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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04282538
Other study ID # 17411953800
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 1, 2018
Est. completion date December 31, 2020

Study information

Verified date February 2020
Source Shanghai Zhongshan Hospital
Contact Xin Wang, MD
Phone 02164041991
Email wang.xin@zs-hospital.sh.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was a prospective, randomized, single-blind, parallel-controlled, multicenter clinical study to evaluate the efficacy and safety of repetitive transcranial magnetic stimulation and transcranial direct current stimulation assisted rehabilitation in the treatment of cerebrovascular disease-related gait disorders.


Description:

This study was a prospective, randomized, single-blind, parallel-controlled, multicenter clinical study. The main purpose was to evaluate the efficacy and safety of repetitive transcranial magnetic stimulation and transcranial direct current stimulation assisted rehabilitation in the treatment of cerebrovascular disease-related gait disorders. The secondary objective was to assess the effects of these two types of neuromodulation on cognitive, emotional, and daily living abilities.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 31, 2020
Est. primary completion date November 30, 2020
Accepts healthy volunteers No
Gender All
Age group 35 Years to 75 Years
Eligibility Inclusion Criteria:

1. Group A: Gait Dysfunction of Hemiplegia

- Age = 35 years old, = 75 years old;

- There was a cerebral infarction event in the past = 2 months, leaving unilateral lower extremity paralysis, muscle strength IV to V- grade;

- Brunnstrom staging: lower limb of paralysis (IV-V grade), lower limb of healthy side (IV-V grade), upper limbs (IV-V grade), hands (IV-V grade);

- Able to stand for 5 minutes without assistance, without gait aid, and to walk independently for 5 minutes without stopping;

- Mini-mental state examination (MMSE) > 17 points, able to complete cognitive and gait assessments.

2. Group B: Frontal Gait Dysfunction

- Age = 35 years old, = 75 years old;

- Meet the frontal gait characteristics: a) Balance dysfunction: wide step base, trunk swing, increased fall, decreased trunk movement control, and autonomous activity dysfunction; b) difficulty in starting, dragging and freezing; c) without limb ataxia, dysarthria, nystagmus, decreased facial expression, decreased upper limb joint activity, upper motor neuron impaired signs, and resting tremor;

- There was a cerebral infarction event = 2 months, or asymptomatic stroke event but the head MRI suggested single or multiple lacunar infarction or ischemic lesion (diameter = 2cm);

- limb muscle strength V- to V grade, and the muscle strength of both limbs is the same;

- Able to stand for 5 minutes without assistance, without gait aid, to walk independently for 5 minutes;

- Able to complete cognitive and gait assessments.

Exclusion Criteria:

- Other gait abnormalities caused by other diseases, such as Parkinson's disease, hydrocephalus, cerebellar disease, vestibular system disease, extrapyramidal abnormalities, abnormalities of proprioceptive sensibility, visual abnormalities, auditory abnormalities, peripheral nerves and musculoskeletal diseases;

- Symptomatic cerebral infarction <2 months; Severe nervous system diseases, such as previous cerebral hemorrhage, history of subarachnoid hemorrhage, craniocerebral trauma, cerebral vascular malformation, brain tumor, central nervous system infection, demyelinating disease, epilepsy, myelopathy, etc.;

- Severe cognitive impairment, major depression, and aphasia disable to finish the cognitive and gait assessments;

- serious cardiovascular, pulmonary, blood, rheumatism and other complications, pregnancy;

- Metal implants such as pacemakers or cochlear implants;

- Taking drugs that affect cortical excitability: such as antiepileptic drugs, sedation, benzodiazepines, antidepressants, dopamine, amphetamines, etc.;

- long-term heavy drinking: the alcohol content of men drinking more than 168g per week, women more than 112g;

- Neurological rehabilitation treatment was received within 1 month before the start of the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Active rTMS
4-week (5 days per week) active rTMS (90%rMT, M1, 10Hz for 10s, 50s interval, 20 trains)
Sham rTMS
4-week (5 days per week) sham rTMS
Active tDCS
4-week (5 days per week) active tDCS (2mA, DLPFC, 20 min)
Sham tDCS
4-week (5 days per week) sham tDCS
Other:
Walking training
4-week (5 days per week) walking training
Cognition training
4-week (5 days per week) cognition training

Locations

Country Name City State
China Shanghai Eighth People's Hospital Shanghai Shanghai
China Shanghai Huadong Hospital Shanghai Shanghai
China Shanghai Sixth People's Hospital Shanghai Shanghai
China Shanghai Tenth People's Hospital Shanghai Shanghai
China Shanghai Xuhui District Central Hospital Shanghai Shanghai
China Shanghai Zhongshan Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
zsneurology

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Velocity of 10m walking test Velocity of 10m walking test (10MWT) according to the video 12 weeks
Secondary 10m walking test Step width, step size, step frequency of 10m walking test (10MWT) according to the video 12 weeks
Secondary Turn time of time up and go test Total time, pace, standing time, turn time of time up and go test (TUGT) according to the video 12 weeks
Secondary Dual-task walking Pace, step width, step size, step frequency, dual task cost of dual-task walking (DTW) according to the video 12 weeks
Secondary Tinetti Balance and Gait Analysis Gait evaluation according to Tinetti Balance and Gait Analysis (Full score: 28. score >= 19 indicates high risk of fall.) 12 weeks
Secondary Mini-mental state examination (MMSE) Cognition evaluation according to Mini-mental state examination (Full score: 30. score <24 indicates cognitive impairment. ) 12 weeks
Secondary Montreal cognitive assessment (MoCA) Cognition evaluation according to Montreal cognitive assessment (Full score: 30. score <26 indicates cognitive impairment. 12 weeks
Secondary Symbol digit modalities test (SDMT) Attention evaluation according to Symbol digit modalities test (Counting number of right modalities in 90s. ) 12 weeks
Secondary Color word test (CWT) Execution evaluation according to Color word test (Counting number of right ones. ) 12 weeks
Secondary Hamilton depression scale (HAMD) Mood evaluation according to Hamilton depression scale (Score >7 indicates possible depression.) 12 weeks
Secondary Instrumental activities of daily living (IADL) Daily living ability evaluation according to Instrumental activities of daily living (Full score: 24. Higher score indicates higher independence. ) 12 weeks
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