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Development and Empirical Study of a Swallowing Rehabilitation Program for Patients with Oral Cancer Based on Timing Theory

Development and Empirical Study of a Swallowing Rehabilitation Program for Patients with Oral Cancer Based on Timing Theory

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106129
Enrollment
Unknown
Registered
2025-07-17
Start date
2025-07-17
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Dysphagia in Patients with Oral Cancer

Interventions

Control group:The control group received a standard rehabilitation care protocol, which included empty swallowing exercises and laryngeal elevation training (5–8 repetitions per movement, performed in
Experimental group:(1) Diagnostic Phase (from diagnosis to admission to the pre-admission preparation center): Information: Provide education on etiology, high-risk factors, clinical manifestations,

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age between 18 and 60 years; 2 Meet the diagnostic criteria for oral cancer; 3 Exhibit swallowing dysfunction, as assessed by a score of Level 3 or higher on the Wada Drinking Water Test combined with the Eating Assessment Tool-10 (EAT-10); 4 Possess clear consciousness, be capable of understanding and cooperating in the completion of swallowing rehabilitation; 5 Family members or caregivers have normal cognitive function and comprehension ability, are proficient in reading and writing Chinese, and are able to communicate via WeChat software; 6 The patient and their family members have provided informed consent and voluntarily agree to participate in this study.

Exclusion criteria

Exclusion criteria: 1 Patients with a history of psychiatric disorders or undergoing specific pharmacological treatment; 2 Patients who have deceased during the study period; 3 Patients currently participating in other similar research studies.

Design outcomes

Primary

MeasureTime frame
The Functional Oral Intake Scale,FOIS;Swallowing-related Quality of Life,SWAL-QOL;

Secondary

MeasureTime frame
Body Mass Index (BMI),;Duration of Nasogastric Tube Retention;

Countries

China

Contacts

Public ContactJian-Wen Hou

Zhejiang Cancer Hospital

945298500@qq.com+86 135 6714 7265

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026