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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05661825
Other study ID # TMU-JIRB N202207042
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2023
Est. completion date October 30, 2023

Study information

Verified date November 2022
Source Taipei Medical University WanFang Hospital
Contact Shiauyee Chen, Master
Phone 1-886-2-29307930
Email shiauyee@tmu.edu.tw
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The benefits of cardiac rehabilitation include improving exercise tolerance and quality of life. However the attending rate of the patients with acute myocardial infarction was low according to the previous studies. This is a retrospective chart review study collecting the basic characteristics of the patients diagnosed with acute myocardial infarction of Wang-Fang Hospital (from Jan 1, 2012 to June 30, 2021). The aims of the studies are to investigate the related issues of cardiac rehabilitation including (1) attending rate (2) the efficacy of exercise training (3) the factors that limit the participation of the training programs.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date October 30, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: 1. Cased diagnosed with acute myocardial infarction at emergent department and admitted 2. Age over 20 years old Exclusion Criteria: 1. AAD cases after admission to ER or the general ward 2. Cases died within admission. 3. Cases refused the treatments.-

Study Design


Intervention

Other:
phase II cardiac rehabilitation
Phase II cardiac rehabilitation was provided in the the department of physical medicine and rehabilitation in Wan Fang Hospital. The programs are two times a week, one session for 30 minutes (30 sessions in total). The training programs are focused on aerobic training with bicycles. The training intensity is calculated with 40% to 80% oxygen consumption reserve from the result of cardiopulmonary exercise test. In case of safety, heart rate, blood pressure, EKG and rate of perceived exertion will be monitored during training.

Locations

Country Name City State
Taiwan Wan-Fang hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of maximal oxygen consumption after intervention The subjects received cardiopulmonary exercise tests before and after training. Baseline, 6 weeks after training, 16 weeks after training
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