Construction and Application of Early Lung Rehabilitation Training Programs

NCT04912986 | Unknown

• 1 other identifier: 2021-0232
• Study Type: interventional
• Target: 38
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Pulmonary Transplantation

Keywords

pulmonary transplantation; pulmonory rehabilitation

Outcome Measures

Primary Outcomes (1)

• Mechanical ventilation time

  The time for mechanical ventilation

  1 year

Study Arms (2)

routine treatment

PLACEBO COMPARATOR

Review the collection of patient-related clinical data, collation of clinical data and outcome indicators

Behavioral: Routine treatment

Experimental group

EXPERIMENTAL

The intervention was implemented in accordance with the Early Lung Rehabilitation Training Programme for Adult Double Lung Transplant Patients

Behavioral: Early Lung Rehabilitation Training

Interventions

Early Lung Rehabilitation Training BEHAVIORAL

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.

Experimental group

Routine treatment BEHAVIORAL

Provide rehabilitation training as usual, without standard program

routine treatment

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• age ≥ 18 years
• consent to early lung rehabilitation
• informed consent to this study.

You may not qualify if:

• Unstable condition, not allowed to receive pulmonary rehabilitation treatment
• A person with a mental disorder who cannot cooperate.

Sponsors & Collaborators

• Second Affiliated Hospital, School of Medicine, Zhejiang University: lead

Study Sites (1)

SAHZhejiangU

Hangzhou, Zhejiang, 310000, China

RECRUITING

Study Officials

• Jiangshuyuan Liang, Master

  Second Affiliated Hospital, School of Medicine, Zhejiang University

  STUDY CHAIR

Central Study Contacts

Jiangshuyuan Liang, Master

CONTACT

13868058705; 2517140@zju.edu.cn

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 31, 2021
• First Posted: June 3, 2021
• Study Start: April 1, 2021
• Primary Completion: September 30, 2022
• Study Completion: December 30, 2023
• Last Updated: June 3, 2021

Record last verified: 2021-05

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)