To Explore the Functional Connectivity Pattern of Cortical Swallowing Network in the Oral Phase of Post-stroke Dysphagia Based on Dynamic Causal Modelling

NCT ID: NCT06564688

Last Updated: 2024-08-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

72 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-20

Study Completion Date

2025-07-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Swallowing activity in the oral phase is regulated by the cortical swallowing network, and the functional connectivity pattern of the cortical swallowing network is related to swallowing activity. The structural damage of the cortical swallowing network and abnormal activation of brain areas related to swallowing in post-stroke dysphagia affect swallowing activity. The recovery of dysphagia after stroke is related to the compensation of swallowing network in the contralateral hemisphere and different connectivity patterns of diseased brain areas, and the integrity of cortical swallowing network connectivity affects the sequence of oral swallowing activities. However, it is not clear how the functional connectivity patterns and interactions of brain regions of the cortical swallowing network related to oral swallowing activity change in patients with oral dysphagia after stroke.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Swallowing is a complex movement consisting of sequential and ordered activation of swallowing muscles interconnected cortical areas that facilitate the complex communication of sensory inputs and motor outputs to control oral movements such as jaw or chewing.During the swallowing task, the cortical swallowing network collaborates with each other to regulate swallowing activity. The damage of the swallowing cortex can affect the coordination of muscle groups in the swallowing process. Compared with healthy people, stroke patients show disordered swallowing movements, which greatly increases the risk of aspiration. Different lesions and connectivity patterns of stroke can affect the prognosis of dysphagia after stroke.In stroke patients with dysphagia, functional brain networks associated with motor control of swallowing were found to be disrupted in acute stroke patients with dysphagia.The recovery of dysphagia after stroke is related to the compensation of swallowing network in the contralateral hemisphere and different connectivity patterns of diseased brain areas, and the integrity of cortical swallowing network connectivity affects the sequence of oral swallowing activities. However, it is not clear how the functional connectivity patterns and interactions of brain regions of the cortical swallowing network related to oral swallowing activity change in patients with oral dysphagia after stroke.The purpose of this study is to explore the specific brain regions that are related to the dynamic changes of the functional connectivity pattern of the cortical swallowing network and the neuroimaging representations of the interbrain interaction in the oral phase of patients with dysphagia after stroke.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dysphagia After Stroke Cortical Swallowing Network Functional Magnetic Resonance Imaging Oral Phase Dynamic Causal Modelling

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Dysphagia in the oral phase after stroke

The swallowing function was assessed by swallowing related scale and the Videofluoroscopic Swallowing Study, and then functional magnetic resonance imaging was performed.

Swallowing function test

Intervention Type DIAGNOSTIC_TEST

The oral function score assesses the oral functional performance of chewing in all participants.

The Functional oral feeding Scale (FOIS) was used to assess the ability of all participants to eat.

The standardized swallowing assessment (SSA) was used to assess the global swallowing function of all participants.

Without dysphagia after stroke

First, the swallowing function related scale was evaluated, and then the functional magnetic resonance imaging (fMRI) scan was performed.

Swallowing function test

Intervention Type DIAGNOSTIC_TEST

The oral function score assesses the oral functional performance of chewing in all participants.

The Functional oral feeding Scale (FOIS) was used to assess the ability of all participants to eat.

The standardized swallowing assessment (SSA) was used to assess the global swallowing function of all participants.

Healthy controls

First, the swallowing function related scale was evaluated, and then the functional magnetic resonance imaging (fMRI) scan was performed.

Swallowing function test

Intervention Type DIAGNOSTIC_TEST

The oral function score assesses the oral functional performance of chewing in all participants.

The Functional oral feeding Scale (FOIS) was used to assess the ability of all participants to eat.

The standardized swallowing assessment (SSA) was used to assess the global swallowing function of all participants.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Swallowing function test

The oral function score assesses the oral functional performance of chewing in all participants.

The Functional oral feeding Scale (FOIS) was used to assess the ability of all participants to eat.

The standardized swallowing assessment (SSA) was used to assess the global swallowing function of all participants.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with dysphagia after first stroke, meeting the diagnostic criteria of stroke, and confirmed by brain CT or brain MRI;
* Oral dysphagia caused by stroke;
* FOIS level ≤ 5; WST level ≥3;
* Those who can understand and carry out the simple instructions of the treatment staff and are willing to accept the examination and treatment;
* Clear consciousness and stable vital signs;
* Patients in the recovery stage with stroke course and dysphagia duration between 0 and 6 months;
* Right-handed;
* Voluntary participants with informed consent.

* Patients with first-ever stroke, meeting the diagnostic criteria of stroke, and confirmed by brain CT or brain MRI;
* No dysphagia, FOIS level =7; WST level =1;
* Those who can understand and carry out the simple instructions of the treatment staff and are willing to accept the examination and treatment;
* Clear consciousness and stable vital signs;
* Patients in the recovery stage with stroke duration between 0 and 6 months;
* Right-handed;
* Voluntary participants with informed consent.

* Normal cognitive function and swallowing function, FOIS level =7; WST level =1;
* Gender and age matched with patients with dysphagia in the oral phase after stroke;
* Right-handed;
* Voluntary participants with informed consent.

Exclusion Criteria

* Dysphagia not caused by stroke or non-oral dysphagia;
* History of cerebral trauma, stroke, brain tumor, cerebrovascular, intracranial infection, Parkinson's disease, epilepsy, or other neurological or psychiatric diseases;
* Symptoms of severe aphasia, neglect, visual field defect and other cortical lesions; Patients with severe cognitive impairment or depression;
* Taking or within 2 weeks of taking drugs that affect the nervous system or psychoses;
* Patients with metal implants and/or spatial claustrophobia who are not suitable for MRI scanning;
* Visual/hearing disorders affecting training and assessment;
* Persons who are participating in other research trials that may influence the results of this study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science

OTHER_GOV

Sponsor Role collaborator

Fujian University of Traditional Chinese Medicine

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Qingqing Zhang

lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Qingqing Zhang

Role: CONTACT

18150019719

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2023KY-015-02

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Fine Motor Skills and Post-Stroke Swallowing
NCT05224973 ACTIVE_NOT_RECRUITING NA