Symptoms, Physical Function, and Recovery in Patients Receiving Lung Cancer Treatment Before Surgery

Official record

Identifier

NCT07853443

Recruiting locations

Locations are not included in the offline baseline for this record. Open the official record to see the current site list.

Interventions studied

Longitudinal Assessment of Symptoms, Physical Function, and Postoperative Recovery

Lead sponsor

Aerospace Center Hospital

Target enrolment

360 participants

Study type

OBSERVATIONAL

Phase

Not provided in the official record

Status

Not yet recruiting

First posted

Oct 1, 2026

Last updated on the registry

Oct 1, 2026

Age

18 Years

Sex

ALL

Study contact

No public contact is listed on the official record.

Eligibility criteria

Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.

Inclusion Criteria:

* Age 18 years or older.

Histologically or cytologically confirmed lung cancer.

Planned neoadjuvant systemic therapy followed by lung resection, as determined by the treating multidisciplinary team.

Enrollment and baseline questionnaire assessment before the first dose of the planned neoadjuvant treatment course.

Able to understand and answer the study questionnaires in Chinese, independently or with standardized assistance from research staff.

Willing to participate in assessments during treatment, before surgery, and during postoperative follow-up.

Provides written informed consent.

Exclusion Criteria:

* The current neoadjuvant treatment course has already started before enrollment and baseline assessment.

Cognitive impairment or another condition that prevents informed consent or reliable self-reported questionnaire responses despite assistance.

Indexed under

Lung Cancer