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Clinical Trials/NCT06458894
NCT06458894RecruitingNot Applicable

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

The Fourth Affiliated Hospital of Zhejiang University School of Medicine1 site in 1 country100 target enrollmentStarted: August 24, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Time to the first ambulation after surgery

Study Overview

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 Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
60 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Time to the first ambulation after surgery

Time Frame: 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

Time Frame: 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 Outcomes

  • Lung function index(30 Days after intervention)

Investigators

Sponsor
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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