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Development and empirical study of sentinel symptom management model for postoperative lung cancer patients undergoing chemotherapy with real-time adaptive intervention

Development and empirical study of sentinel symptom management model for postoperative lung cancer patients undergoing chemotherapy with real-time adaptive intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112401
Enrollment
Unknown
Registered
2025-11-13
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-11-17

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:The Intervention group received four chemotherapy cycles of gastrointestinal symptom management interventions in addition to standard care. As chemotherapy progressed, the intervent
Control group:Control group patients receive standard care. Before chemotherapy, they receive one-on-one briefings covering basic chemotherapy knowledge, precautions before, during, and after treatmen

Sponsors

Liaoning University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Pathological diagnosis of lung cancer; 2. Planned to receive at least 4 cycles of chemotherapy post-surgery; 3. Age >= 18 years.

Exclusion criteria

Exclusion criteria: 1. Recurrence or metastasis of lung cancer; 2. Coexisting moderate to severe cognitive or psychiatric disorders; 3. Coexisting severe diseases of vital organs such as heart, brain, or kidney.

Design outcomes

Primary

MeasureTime frame
Gastrointestinal symptoms;

Secondary

MeasureTime frame
Quality of life ;

Countries

China

Contacts

Public ContactMa Jingshuang

Liaoning University of Traditional Chinese Medicine

723494553@qq.com+86 188 4242 8125

Outcome results

None listed

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