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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06458894
Enrollment
100
Registered
2024-06-14
Start date
2024-08-24
Completion date
2026-12-26
Last updated
2025-02-17

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

Conditions

Lung Cancer

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.

Interventions

BEHAVIORALPrerehabilitation

Home prerehabilitation was performed on the basis of routine preoperative preparation

Sponsors

The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
60 Years to 99 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Time to the first ambulation after surgery3 Weeks after interventionPatients can complete the time of walking at the bed, and unplanned extubation
Dwelling time of chest drain and chest drainage flowTwo days after the interventionThe duration of the postoperative chest drain and the chest on postoperative day 1 and postoperative day 2 were recorded Lead the flow

Secondary

MeasureTime frameDescription
Lung function index30 Days after interventionPulmonary 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

Countries

China

Contacts

Primary Contactchaoqian li
13858066862@163.com13858066862

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026