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A Qualitative Study on the Nursing Experience of Neoadjuvant Treatment with Toripalimab Combined with Chemotherapy for Head and Neck Malignancies.

A Qualitative Study on Nursing Care for Patients with Head and Neck Malignancies Undergoing Neoadjuvant therapy with Toripalimab Injection with Chemotherapy.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107851
Enrollment
Unknown
Registered
2025-08-20
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

locally advanced head and neck squamous cell carcinoma (HNSCC), including but not limited to oral cancer, oropharyngeal cancer, laryngeal cancer, and hypopharyngeal cancer.

Interventions

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The patient or their legal guardian agrees to participate in the study, voluntarily joins the study, and signs the informed consent form. 2. Patients with head and neck malignant tumors who are aged >=18 years. 3. Confirmed by pathology or cytology, and suitable for neoadjuvant treatment with toripalimab in combination with chemotherapy. 4. Patients with complete clinical data and nursing records, who can provide information about their treatment experience and nursing perceptions. 5. Case records of patients who receive neoadjuvant treatment with toripalimab in combination with chemotherapy during the study period.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to participate in the study or are unable to provide informed consent. 2. Patients with severe dysfunction of important organs such as the heart, lungs, liver, or kidneys, which may affect the evaluation of treatment outcomes. 3. Patients who are simultaneously participating in other clinical trials that may influence the results of this study. 4. Cases lacking key information (such as nursing interventions or patient feedback). 5. Cases where patients develop significant complications during treatment or are transferred to other medical institutions, resulting in an incomplete record of the nursing process. 6. Patients with mental illness or cognitive impairment.

Design outcomes

Primary

MeasureTime frame
The psychological experience, physical sensation, and subjective perception of nursing needs of patients during and after treatment.;

Secondary

MeasureTime frame
Knowledge mastery level;Improvement in quality of life;Improvement of self-care ability;

Countries

China

Contacts

Public ContactHu Zidan

Shenzhen Second People's Hospital

2334234175@qq.com+86 755 8336 6388

Outcome results

None listed

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