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Application of lung rehabilitation nursing program based on behavior change wheel theory in patients with oral and maxillofacial malignant tumors

Application of lung rehabilitation nursing program based on behavior change wheel theory in patients with oral and maxillofacial malignant tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099236
Enrollment
Unknown
Registered
2025-03-20
Start date
2025-04-18
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Oral and maxillofacial malignant tumors

Interventions

Experimental group:The research team customized the pulmonary rehabilitation nursing program based on previous evidence.
Control group:Routine rehabilitation

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for qualitative interview subjects: Patients diagnosed with postoperative head and neck tumors; voluntarily participate in this study and sign the informed consent. Inclusion criteria for intervention program verification: 1.Patients diagnosed with oral and maxillofacial tumors by pathology or imaging examination. 2.Patients who have not undergone oral and maxillofacial tumor resection. 3.Age >= 18 years old. 4.Informed consent: Patients voluntarily participate in this study and sign the informed consent. 5.Patients who can undergo pulmonary function testing throughout the course of the disease.

Exclusion criteria

Exclusion criteria: Exclusion criteria for qualitative interview subjects: patients with unstable emotions and medical conditions. Exclusion criteria for intervention program verification: 1.Patients with other serious lung diseases, such as bronchial asthma, malignant tumors, etc.; 2.Patients with serious cardiovascular diseases, such as acute myocardial infarction, heart failure, etc.; 3.Patients with neurological and psychiatric diseases; 4.Patients with severe complications after surgery who are unable to undergo routine rehabilitation training; 5.Patients with severe hypoxemia (SpO2 < 80%), gastrointestinal tract, cardiovascular system and other adverse reactions during the 6-minute walk test (6MWT). 6.Patients with severe cognitive dysfunction who are unable to cooperate with lung function and exercise endurance assessments.

Design outcomes

Primary

MeasureTime frame
Lung function, including forced expiratory volume in first second (FEV1), forced vital capacity (FVC), peak expiratory flow (PEF);

Secondary

MeasureTime frame
Sports endurance;Quality of Life;Cancer-related Fatigue (CFS);

Countries

China

Contacts

Public ContactXiaoqin Bi

West China Hospital of Stomatology, Sichuan University

hxbxq@163.com+86 135 4116 8806

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026