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Application of a Prehabilitation System for Swallowing Assessment and Feeding Training in Postoperative Hypopharyngeal Cancer Patients

Application of a Prehabilitation System for Swallowing Assessment and Feeding Training in Postoperative Hypopharyngeal Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107502
Enrollment
Unknown
Registered
2025-08-13
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Hypopharyngeal cancer

Interventions

Control group :The control group adopted the conventional nursing process: 1. Improve preoperative and postoperative evaluation and education
2. Improve guidance on perioperative catheterization, airway, condition, nutrition, and other related aspects
3. When trying to eat, guide the patient to press against the tracheal tube opening and take a sitting position
The nurse observes the patient for coughing, aspiration, and other symptoms while eating
4. Follow up by phone for 6 weeks after discharge and receive routine education.
experimental group:On the basis of the control group, the experimental group was intervened with a pre rehabilitation system during the perioperative period. The doctor prescribed a trial meal for eva

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with nasopharyngeal cancer through intraoperative rapid frozen pathological examination or postoperative routine paraffin section pathological examination; 2. The postoperative wound has healed well and the stitches have been removed, but the patient has been placed in a gastric tube without self feeding; 3. Having good compliance; 4. The patient is conscious, able to communicate normally, and has no serious cognitive impairment or mental illness; 5. Willing to participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1.heart, liver, kidney, hematopoietic and immune system diseases; 2. Patients with unstable condition or death within one month after surgery; 3. Postoperative poor local healing, pharyngeal leakage, poor overall condition, and inability of local anatomical structures to eat independently.

Design outcomes

Secondary

MeasureTime frame
Clinical indicators;Incidence of complications;

Primary

MeasureTime frame
Swallowing function indicators;

Countries

China

Contacts

Public ContactZhu Lijuan

Shanghai General Hospital

18917970733@126.com+86 189 1797 0733

Outcome results

None listed

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