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Using patient-reported outcomes to manage postoperative symptoms in patients with lung cancer: a multicentre, randomised controlled trial

A study for perioperative symptom management in patients with lung cancer based on patient-reported outcomes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020846
Enrollment
Unknown
Registered
2019-01-21
Start date
2019-03-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

lung cancer

Interventions

PRO-based group:PRO-based symptom management measures
Traditional model group:Routine symptom management measures

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-75 years; (2) clinical diagnosis of primary lung cancer; (3) clinical staged I-IIIA (8th edition); (4) plan to receive surgery; (5) Be able to and willing to respond to a repeated electronic questionnaire (e-questionnaire) on a smartphone or a tablet.

Exclusion criteria

Exclusion criteria: (1) History of neoadjuvant therapy; (2) have other malignant tumors; (3) unable to understand the research content; (4) History of chest surgery; (5) Daily analgesics use.

Design outcomes

Primary

MeasureTime frame
Mean symptom threshold events;—

Secondary

MeasureTime frame
Trajectory of symptom intensity;Trajectory of daily function recovery;Trajectory of quality of life recovery;Revisit rate after discharge;—

Countries

China

Contacts

Public ContactDai Wei

Sichuan Cancer Hospital

daiwei@sichuancancer.org+86 18508222758

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026