Research on Building and Application of Internet-based Home Pre-rehabilitation Model for Lung Surgery Patients.

Not Applicable

Recruiting

• Conditions: Lung Cancer
• Interventions: Behavioral: Prerehabilitation

• Registration Number: NCT06458894
• Lead Sponsor: The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Brief Summary

This study, based on the Internet platform, involving family caregivers in preoperative management, not only promotes patient compliance with preoperative rehabilitation exercise, but also provides multi-way rehabilitation measures for elderly patients with limited mobility or medical difficulties, and also provides new ideas for other specialties。

Detailed Description

This study using a randomized controlled trial, 100 patients that meet the inclusion criteria are divided into experimental group and control group, experimental group adopts routine nursing measures, intervention group for preoperative family rehabilitation training, intervention for 2 weeks, observe the first after surgery, lung function index, chest catheterization days, postoperative hospital stay and medical expenses.

Study Timeline

• Study First Submitted: 2024-06-11
• Study First Submitted QC: 2024-06-11
• Study First Posted: 2024-06-14
• Study Start: 2024-08-24
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-14
• Last Update Posted: 2025-02-17
• Primary Completion: 2025-12-25
• Study Completion: 2026-12-26

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

1. Age ≥ 60 years old; 2. A preliminary diagnosis of pulmonary结节 or lung tumor by chest CT; 3. Planning to undergo thoracoscopic lung resection surgery; 4. Voluntary participation of patients.

Exclusion Criteria

1. Patients with severe condition who cannot tolerate pre-rehabilitation training; 2. Patients with consciousness disorder or mental abnormalities who cannot cooperate with pre-rehabilitation training; 3. Patients who cannot complete questionnaire filling out due to visual, auditory, or intellectual impairment, etc.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
There were no interventions	Prerehabilitation	Give guidance on respiratory function exercise
Prerehabilitation	Prerehabilitation	Give guidance on respiratory function exercise

Primary Outcome Measures

Name	Time	Method
Time to the first ambulation after surgery	3 Weeks after intervention	Patients can complete the time of walking at the bed, and unplanned extubation
Dwelling time of chest drain and chest drainage flow	Two days after the intervention	The duration of the postoperative chest drain and the chest on postoperative day 1 and postoperative day 2 were recorded Lead the flow

Secondary Outcome Measures

Name	Time	Method
Lung function index	30 Days after intervention	Pulmonary function test was performed with the pulmonary function detector on the day of the patient and 30 days after surgery Guide the patient to do inhale or exhale with maximum effort, make three consecutive measurements, and record the best results, including Forced expiratory volume at second 1

Trial Locations

Locations (1)

The Fourth Affiliated Hospital of Zhejiang University School of Medicine; 🇨🇳 Yiwu, Zhejiang, China