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Evaluation of the intervention effect of patient activation intervention on the compliance of respiratory exercise in lung cancer patients undergoing chemotherapy

Evaluation of the intervention effect of patient activation intervention on the compliance of respiratory exercise in lung cancer patients undergoing chemotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123036
Enrollment
Unknown
Registered
2026-04-21
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Lung cancer

Interventions

Intervention group:Compliance intervention based on patient activation + routine nursing
Control group:routine nursing

Sponsors

Jiangnan University; Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Meet the criteria of being diagnosed with lung cancer through pathological or cytological examination; 2. Be currently undergoing or have completed at least one chemotherapy cycle; 3. Be aged >= 18 years; 4. Have a score of = 90%; 7. According to the judgment of the attending doctor or the assessment of the Palliative Performance Scale (PPS), have an expected survival time >= 3 months and no major changes in the treatment plan during the intervention period; 8. Give informed consent and voluntarily participate in the study; 9. Be conscious, have certain understanding and communication abilities, and be able to complete the survey independently or with the assistance of the investigators.

Exclusion criteria

Exclusion criteria: 1. Presence of acute, uncontrolled, or decompensated medical diseases, as well as communication disorders or mental illnesses; 2. Currently undergoing mechanical ventilation or diagnosed by a doctor with acute respiratory distress syndrome; 3. Those with a large amount of malignant pleural effusion or a large amount of pericardial effusion at risk of cardiac tamponade; 4. Presence of other severe organ dysfunctions; 5. Unaware of the condition.

Design outcomes

Primary

MeasureTime frame
Compliance with breathing exercises;Patient Activation;

Countries

China

Contacts

Public ContactTeng Liping

Wuxi Medical School of Jiangnan University; Affiliated Hospital of Jiangnan University

18726598539@163.com+86 187 2659 8539

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026