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Investigating the Brain Network Mechanisms Underlying Enhanced Laryngeal Elevation Training for Swallowing Disorder Recovery in Stroke Patients Using Near-Infrared Imaging Technology

Investigating the Brain Network Mechanisms Underlying Enhanced Laryngeal Elevation Training for Swallowing Disorder Recovery in Stroke Patients Using Near-Infrared Imaging Technology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119473
Enrollment
Unknown
Registered
2026-02-27
Start date
2024-07-16
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Control group:Standard swallowing function training includes oral sensory training, oral motor training, swallowing technique strategies, and other techniques. Training sessions are 30 minutes each, o
Treatment group:A biofeedback device that combines conventional swallowing exercises with enhanced pharyngeal elevation.

Sponsors

Shandong Provincial Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Must meet the diagnostic criteria outlined in the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke (2014 Edition) or the Chinese Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage (2014 Edition), and be confirmed by cranial CT or MRI; 2. First-time onset or previous episodes without residual dysphagia, aged 18-75 years, and disease duration =17 for illiterate individuals, >=20 for elementary school graduates, >=24 for middle school graduates), basic auditory comprehension intact, alert consciousness, and ability to cooperate with assessment and treatment; 5. Inform patients and families of precautions and obtain signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with cognitive impairment, dementia, psychiatric disorders, or psychological disorders; 2. Following radiotherapy for oral, head, or neck tumors; 3. Concurrent severe organic diseases such as cardiac, pulmonary, hepatic, or renal conditions; 4. Individuals with swallowing dysfunction due to other causes; 5. Participants who may discontinue treatment prematurely due to factors affecting swallowing therapy; 6. Presence of intracranial metal implants, metallic pacemakers, or cranial defects.

Design outcomes

Primary

MeasureTime frame
Televised and Clinical Fluoroscopic Swallowing Studies;

Secondary

MeasureTime frame
Leakage and False Suction Scoring;Functional Oral Intake Scale;Functional near-infrared spectroscopy;

Countries

China

Contacts

Public ContactMeng Yang

Shandong Provincial Third Hospital

494571910@qq.com+86 187 6401 6058

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026