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Clinical Trials/NCT07149935
NCT07149935RecruitingNot Applicable

Continuous Effect Of Long-Term Rehabilitation Training On Clinical Improvement(TTCI) And Cardiopulmonary Function In Pulmonary Arterial Hypertension Patients- A Multicenter-randomisation Study

RenJi Hospital1 site in 1 country104 target enrollmentStarted: September 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
104
Locations
1
Primary Endpoint
6 minutes walk distance( 6MWD)

Study Overview

Brief Summary

This multicenter, open label, double-arm study aims at investigating the the continuous effect of long-Term rehabilitation training on clinical improvement(ITTCI) and cardiopulmonary function in pulmonary arterial hypertension patients

Detailed Description

Pulmonary Arterial Hypertension (PAH) is a disease caused by various reasons leading to pulmonary vascular remodelling and then results in a progressive increase in pulmonary vascular resistance and right heart failure. PAH progresses rapidly,with a poor prognosis. Targeted drugs has brought about an improvement in the quality of life of patients with PAH. However, in most cases, patients' clinical symptoms will be gradually worsen with exercise capacity gradually declining. The prognosis of PAH remains bleak. Although exercise was previously considered as a relative contraindication for PAH patients , a growing body of research has found that exercise rehabilitation is safe and effective for them. Patients show greater improvement in their symptoms and quality of life. Effective and appropriate exercise rehabilitation in low- and middle-income countries can maximise the therapeutic benefits of targeted medication, improve patient survival rate, and enhance exercise tolerance and cardiorespiratory fitness. In this study, we will investigate the continuous effects of exercise rehabilitation on the clinical improvement (time to clinical improvement, TTCI) and cardiorespiratory fitness over a 1-year period of long-term rehabilitation, including aerobic training (aerobic power cycling and treadmill walking) and inspiratory muscle training (respiratory trainer and lip-contracting abdominal breathing).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Masking Description

Because the specificity of rehabilization, it is not suitable for us to mask

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients who suffered from pre-capillary PAH (mPAP ≥ 20 mmHg, PVR > 2 Woods unit, PAWP ≤ 15 mmHg) confirmed by right heart catheterisation.
  • •Patients who are in the status of WHO-FC I-III.
  • •Patients between 18 and 75 years old
  • •Female subjects are not pregnant.
  • •Patients are treated with PAH-targeted drugs and are in a stable state and there is no progress of disease).
  • •Patients have not received exercise rehabilitation training within six months.

Exclusion Criteria

  • •Patients with the following diseases or symptoms:
  • •Pulmonary vascular occlusive disease
  • •Respiratory diseases
  • •Ischaemic heart disease, complex congenital heart disease (e.g., tetralogy of Fallot, etc.), cardiomyopathy, valvular disease
  • •Active liver disease
  • •Severe kidney disease
  • •Motor disorders (e.g. lower limb fracture, ataxia, etc.)
  • •Malignant tumour diseases
  • •Physical disability
  • •Hb ≤ 80g / L
  • •Systolic blood pressure ≤85mmHg
  • •History of syncope within 3 months
  • •History of supraventricular or ventricular arrhythmia at rest within 3 months.

Arms & Interventions

rehabilitation training

Experimental

open label

Intervention: Rehabilitation Training (Other)

control

No Intervention

open label

Outcomes

Primary Outcomes

6 minutes walk distance( 6MWD)

Time Frame: every 3 months, until 6 months

The walk distance of patients in 6 minutes

Improved Time To Clinical Improvement(ITTWI)

Time Frame: every 3 months, until 6months

The time that required from the time of rehabilitation training to the first occurrence of at least one stratum improvement of the weber classification

Secondary Outcomes

  • SF-36 score(every 3 months, until 6months)
  • Echocardiographic index---right ventricle(every 3 months, until 6 months)
  • Echocardiographic index---left ventricle(every 3 months, until 6months)
  • CPET index(every 3 months, until 6months)
  • Echocardiographic index-others(every 3 months, until 6months)
  • Echocardiographic index---left ventricle(every 3 months, until 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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