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Efficacy Analysis of Craniocervical Sacral Therapy Based on Posture Characteristic Analysis on Swallowing Function After Stroke

Efficacy Analysis of Craniocervical Sacral Therapy Based on Posture Characteristic Analysis on Swallowing Function After Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125277
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-01-07
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

stroke

Interventions

control group:Based on the clinical manifestations of swallowing disorders in patients, select and develop appropriate and targeted swallowing training programs.
experimental group:In addition to the treatment given to the control group, the Craniosacral Therapy based on postural characteristic analysis was administered for 20 minutes each session, once daily,

Sponsors

Jiaxing Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for stroke formulated at the 6th National Conference on Cerebrovascular Disease; 2. Age range: 18-80 years old; 3. The patient has clear consciousness, stable vital signs, and can cooperate to complete the assessment and treatment; 4. Having swallowing dysfunction, the Wada drinking water test is rated as level II-V; 5. The patient provides informed consent and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with intracranial hypertension (such as cerebral edema, cerebral hemorrhage) and skull fractures; 2. Patients undergoing bone flap decompression; 3. Patients with coagulation dysfunction; 4. Patients with severe cognitive impairment; 5. Merge serious primary diseases such as cardiovascular, liver, kidney, digestive system, etc; 6. Patients with previous spinal cord injuries or spinal cord related diseases; 7. Patients with magnetic metal implants in their bodies; 8. Pregnant patients; 9. Patients who are unable to remain still or cooperate during treatment or evaluation.

Design outcomes

Primary

MeasureTime frame
video fluoroscopic swallowing study;modified barium swallow impairment profile;Functional Magnetic Resonance Imaging;

Secondary

MeasureTime frame
Body posture data measurement;Surface Electromyography;

Countries

China

Contacts

Public ContactXu Danni

Jiaxing Second Hospital

2315831430@qq.com+86 186 6737 2188

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026