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Recruiting NCT06458894

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

No phase Interventional Lung Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Prerehabilitation.
Who it may be relevant to
Registry conditions: Lung Cancer. Basic parameters: 60 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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

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

Primary outcome measures

  • Time to the first ambulation after surgery [Time frame: 3 Weeks after intervention]
  • Dwelling time of chest drain and chest drainage flow [Time frame: Two days after the intervention]
Secondary outcome measures (1)
  • Lung function index [Time frame: 30 Days after intervention]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

China · 1 center
  • The Fourth Affiliated Hospital of Zhejiang University School of Medicine — Yiwu

Identifiers

NCT: NCT06458894 · KY-2024-102

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗