To hear about similar clinical trials, please enter your email below
Trial Title:
Research on Building and Application of Internet-based Home Pre-rehabilitation Model for Lung Surgery Patients.
NCT ID:
NCT06458894
Condition:
Lung Cancer
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Supportive Care
Masking:
Double (Participant, Care Provider)
Intervention:
Intervention type:
Behavioral
Intervention name:
Prerehabilitation
Description:
Home prerehabilitation was performed on the basis of routine preoperative preparation
Arm group label:
Prerehabilitation
Arm group label:
There were no interventions
Other name:
ulmonary function
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.
Criteria for 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.
Gender:
All
Minimum age:
60 Years
Maximum age:
99 Years
Healthy volunteers:
Accepts Healthy Volunteers
Start date:
June 24, 2024
Completion date:
December 26, 2026
Lead sponsor:
Agency:
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Agency class:
Other
Source:
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06458894
