Evidence based construction of preoperative pre health compound plan for patients undergoing thoracoscopic radical resection of lung cancer and its effectiveness evaluation

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400084960

Enrollment

Unknown

Registered

2024-05-28

Start date

2024-06-01

Completion date

Unknown

Last updated

2024-06-03

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:Evidence based pre operative rehabilitation formula for patients undergoing thoracoscopic radical resection of lung cancer

control group:usual care

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: ? All were confirmed to be primary lung cancer through imaging examination and pathological examination; ? Those who plan to undergo thoracoscopic radical surgery for lung cancer; ? Age>18 years old; ? Informed consent and voluntary acceptance of the researcher.

Exclusion criteria

Exclusion criteria: ? There is already a distant metastasis; ? Individuals with other serious diseases such as heart, brain, and kidney; ? Individuals with physical or cognitive impairments who are unable to cooperate; ? Patients with a history of lung surgery.

Design outcomes

Primary

Measure	Time frame
Retention time of thoracic drainage tube;Postoperative complications;The level of knowledge, belief, and practice in pre rehabilitation;	—

Secondary

Measure	Time frame
First time getting out of bed after surgery;Postoperative hospitalization duration;	—

Countries

China

Contacts

Public ContactPing Cai

Affiliated Hospital of Jiangnan University

1099974308@qq.com+86 138 6170 6586

Outcome results

None listed

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