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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05648552
Other study ID # 2022-LCYJ-PY-27
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date December 31, 2025

Study information

Verified date March 2023
Source The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Contact Wenjun Hong
Phone +86 13851924571
Email hongwenjun1989@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The current study aims to reveal the SC-FC coupling pattern and its relationship with motor function in post-stroke survivors with motor dysfunction by multimodal MRI.


Description:

Stroke is the leading cause of death and disability in China. Recently, many previous studies suggested exploring the functional reorganization of the motor function among post-stroke survivors is urgent to be solved in both clinical work and applied basic research. Investigating the structural connectivity (SC) of the brain could visualize the anatomical connections between different brain regions and exploring the functional connectivity (FC) could reveal the functional activity patterns of the human brain in resting- and task- states. Previous studies suggested that SC-FC coupling analysis may shed light on exploring biological markers for the assessment and treatment of motor deficits in post-stroke survivors. The current study aims to reveal the SC-FC coupling pattern and its relationship with motor function in post-stroke survivors with motor dysfunction by multimodal MRI.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date December 31, 2025
Est. primary completion date June 30, 2025
Accepts healthy volunteers
Gender All
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria: 1. Comply with the diagnostic criteria of "Stroke" in the 2010 "Guidelines for the Prevention and Treatment of Cerebrovascular Diseases in China," and confirmed by head CT or MRI. 2. First onset unilateral subcortical stroke (basal ganglia, thalamus, internal capsule, corona radiata, lateral ventricles, etc.). 3. Age ranged from 30 to 75 years old. 4. Right-handedness before stroke. 5. Greater than three months since stroke onset and Brunnstrom graded as III-VI; 6. The condition and vital signs are stable. 7. Sign the informed consent form. Exclusion Criteria: 1. Any contraindications for the MRI examination. 2. History of other brain diseases and drug dependency. 3. Unstable conditions or accompanied by malignant and rapidly progressing diseases, such as severe atrial fibrillation. 4. Serious communication barriers, cognitive impairment, or cooperation with difficulties.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Nanjing Drum Tower Hospital Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Structural-functional Connectivity Coupling The coupling between structural connectivity and functional connectivity Within 1 week after enrollment
Primary Fugl-Meyer Assessment Assessing the motor function in post-stroke participants Within 1 week after enrollment
Secondary Chinese version of Modified Barthel Index Assessing the activities of daily living in post-stroke participants Within 1 week after enrollment
Secondary Broetz Hand Test Assessing the hemiplegic hand performance in post-stroke participants Within 1 week after enrollment
Secondary Placebo Questionnaire Self-evaluation of rehabilitation treatment in post-stroke participants Within 1 week after enrollment
Secondary Hamilton Depression Rating Scale Assessing the depression in post-stroke participants Within 1 week after enrollment
Secondary Chinese (Putonghua) Version of Oxford Cognitive Screen Assessing the cognition in post-stroke participants Within 1 week after enrollment
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