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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04912986
Other study ID # 2021-0232
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date December 30, 2023

Study information

Verified date May 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Jiangshuyuan Liang, Master
Phone 13868058705
Email 2517140@zju.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is intended to construct early lung rehabilitation training programs for adult patients after double lung transplantation, including safety assessment, exercise training, respiratory function training, psychological support and health education, with a view to helping double lung transplant patients achieve lung rehabilitation at an early date, improve patients' motor endurance and respiratory function, and improve the quality of near- and long-term survival.


Description:

The first stage constructs the lung rehabilitation program, and the second stage implements the non-contemporaneous study control trial.


Recruitment information / eligibility

Status Recruiting
Enrollment 38
Est. completion date December 30, 2023
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age = 18 years - consent to early lung rehabilitation - informed consent to this study. Exclusion Criteria: - Unstable condition, not allowed to receive pulmonary rehabilitation treatment - A person with a mental disorder who cannot cooperate.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Early Lung Rehabilitation Training
It is implemented in accordance with the Early Lung Rehabilitation Training Program for Adult Double Lung Transplant Patients. Establish multidisciplinary collaboration teams, including competent doctors, nurses, rehabilitation physicians, and psychologists.
Routine treatment
Provide rehabilitation training as usual, without standard program

Locations

Country Name City State
China SAHZhejiangU Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mechanical ventilation time The time for mechanical ventilation 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT04731792 - Therapeutic Virtual Reality: Helps Reduce Anxiety and Pain During Bronchial Fibroscopies in Lung Transplant Patients. N/A