Skip to content

A Clinical investigation on nutrition and prognosis of patients with head and neck cancers treated by radiotherapy with pre-rehabilitation

A Clinical investigation on nutrition and prognosis of patients with head and neck cancers treated by radiotherapy with pre-rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094151
Enrollment
Unknown
Registered
2024-12-17
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Head and neck cancers

Interventions

The observation group:A standardized swallowing therapy, in conjunction with respiratory muscle exercises, was initiated two weeks prior to the commencement of radiotherapy and continued for a duratio
control group:Post-radiotherapy, a standardized swallowing therapy combined with respiratory muscle exercises was initiated, and this continued for a duration of 3 months.

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) All were diagnosed as head and neck tumors for the first time by imaging and pathological examination. 2) Aged between 18 and 80; 3) Plan to receive radiotherapy and have no previous history of radiotherapy; 4) No cognitive dysfunction, able to correctly understand the relevant content of the experiment and correctly fill in the questionnaire; 5) Can cooperate with the completion of swallowing function assessment, 6min walking experiment, respiratory function assessment, etc 6) Agree to participate in the experiment and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with significant abnormalities in electrocardiogram, laboratory examination and chest radiograph within 1 week of inclusion; 2) Patients with other types of malignant tumors; 3) Patients with respiratory muscle training contraindications 4) Patients with cardiac pacemaker implantation who cannot cooperate with human body composition determination 5) Patients with severe cognitive impairment or mental illness 6) Patients who refused to participate in this clinical trial

Design outcomes

Primary

MeasureTime frame
(videofluroscopic swallowing study,VFSS);(eating assessment tool—10,EAT—10);(Volume-Viscosity Swallow Test,V-VST);(Nutritional risk screening, NRS-2002);(Patient-Generated Subjective Global Assessment,?PG-SGA);(skeletal muscle mass,SMM);water swallow test;(repetitive saliva swallowing test ,RSST);(b;

Secondary

MeasureTime frame
(EORTC QLQ-C30);(Maximal Inspiratory Pressure,PImax);(Maximal Expiratory Pressure,PEmax);(cough peak expiratory flow,PCF);serum albumin;serum total protein;hemoglobin;

Countries

China

Contacts

Public ContactXiang Jie

Affiliated Hospital of Xuzhou Medical University

Xj1111@163.com+86 137 7597 0412

Outcome results

None listed

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