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

Lung Cancer Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06458894
• Other study ID #: KY-2024-102
• Status: Not yet recruiting
• Phase: N/A
• Start date: June 24, 2024
• Est. completion date: December 26, 2026

Study information

• Verified date: June 2024
• Source: The Fourth Affiliated Hospital of Zhejiang University School of Medicine
• Contact: chaoqian li
• Phone: 13858066862
• Email: 13858066862[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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。

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: December 26, 2026
• Est. primary completion date: December 25, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 60 Years to 99 Years

Eligibility

Inclusion Criteria:

1. Age = 60 years old; 2. A preliminary diagnosis of pulmonary?? 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.

Related Conditions & MeSH terms

• Lung Cancer

Intervention

Behavioral:
• Prerehabilitation
Home prerehabilitation was performed on the basis of routine preoperative preparation

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to the first ambulation after surgery	Patients can complete the time of walking at the bed, and unplanned extubation	3 Weeks after intervention
Primary	Dwelling time of chest drain and chest drainage flow	The duration of the postoperative chest drain and the chest on postoperative day 1 and postoperative day 2 were recorded Lead the flow	Two days after the intervention
Secondary	Lung function index	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	30 Days after intervention