Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05201274
Other study ID # BST-AMI
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 11, 2021
Est. completion date February 11, 2023

Study information

Verified date January 2022
Source Shenyang Northern Hospital
Contact Meili Liu, MD
Phone 86-18940193302
Email liumeili1983bl@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acute myocardial infarction (AMI) is one of the leading causes of death around the world, with the potential for substantial morbidity and mortality. The increasing evidence indicates that exercise training has beneficial effects on LV remodelling in post-MI patients with greater benefits occurring when training earlier following MI, among which the earliest time for rehabilitation is one week after myocardial infarction. However, the effect of Baduanjin sequential therapy for patients after one week of AMI has yet to be assessed. Therefore, the aim of this study is to assess the impact of Baduanjin sequential therapy on cardiac and physical function in patients with AMI and reduced ejection fraction after primary PCI.


Recruitment information / eligibility

Status Recruiting
Enrollment 140
Est. completion date February 11, 2023
Est. primary completion date February 11, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Acute myocardial infarction undergoing primary percutaneous coronary intervention; - Aged 18 years or over and under 80 years; - 35% < LVEF < 50% and LV < 65mm; - With informed consents Exclusion Criteria: - Severe symptomatic congestive heart failure (KILLIP cardiac function class III-IV); - Malignant arrhythmias (ventricular fibrillation, ventricular tachycardia, frequent multiple source ventricular premature); - Uncontrolled hypertension (systolic blood pressure greater than 160mmhg, diastolic blood pressure greater than 100mmhg); - Life-threatening diseases with limited life expectancy <6 months; - Inability or difficulty to exercise; - Participation in other clinical trials

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Baduanjin sequential therapy
A detailed description of a standardized Baduanjin exercise protocol complied with the "Health Qigong Baduanjin Standard" enacted by the General Administration of Sports in 2003.
Aerobic exercise
Participants allocated to the usual exercise control group receive a closely supervised, group-format aerobic exercise program located at home or cardiac rehabilitation centre lasting 3 months. The program is consistent with the current recommended guidelines of moderate-intensity exercises for MI.

Locations

Country Name City State
China General Hospital of Shenyang Military Region Shenyang Liaoning

Sponsors (1)

Lead Sponsor Collaborator
Shenyang Northern Hospital

Country where clinical trial is conducted

China, 

References & Publications (4)

Haykowsky M, Scott J, Esch B, Schopflocher D, Myers J, Paterson I, Warburton D, Jones L, Clark AM. A meta-analysis of the effects of exercise training on left ventricular remodeling following myocardial infarction: start early and go longer for greatest e — View Citation

Ibanez B, James S, Agewall S, Antunes MJ, Bucciarelli-Ducci C, Bueno H, Caforio ALP, Crea F, Goudevenos JA, Halvorsen S, Hindricks G, Kastrati A, Lenzen MJ, Prescott E, Roffi M, Valgimigli M, Varenhorst C, Vranckx P, Widimský P; ESC Scientific Document Gr — View Citation

Perelshtein Brezinov O, Klempfner R, Zekry SB, Goldenberg I, Kuperstein R. Prognostic value of ejection fraction in patients admitted with acute coronary syndrome: A real world study. Medicine (Baltimore). 2017 Mar;96(9):e6226. doi: 10.1097/MD.00000000000 — View Citation

Yeh RW, Sidney S, Chandra M, Sorel M, Selby JV, Go AS. Population trends in the incidence and outcomes of acute myocardial infarction. N Engl J Med. 2010 Jun 10;362(23):2155-65. doi: 10.1056/NEJMoa0908610. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other The occurrence and composite of major adverse cardiac and cerebrovascular event (MACCE) defined as recurrent myocardial infarction, any revascularization, readmission, stent thrombosis (ST) all-cause death and stroke) baseline and 3 months
Other Adverse events related to exercise rehabilitation Adverse events related to exercise rehabilitation, such as fall. baseline and 3 months
Primary Left ventricular ejection fraction (LVEF) The change in echocardiographic measures of left ventricular ejection fraction,(LVEF). LVEF in %. baseline and 3 months
Secondary SF-36 the SF-36 has 36 items grouped in 8 dimensions: physical functoning, physicial and emotional limitations, social functioning, bodily pain, general and mental health. baseline and 3 months
Secondary Generalized Anxiety Disorder 7-item (GAD-7) The Generalized Anxiety Disorder 7 (GAD-7) is a 7-item instrument used to briefly measure or assess one of the most common mental disorders. baseline and 3 months
Secondary Patient Health Questionnaire (PHQ-9) The PHQ-9 is the depression module, which scores each of the nine DSM-IV criteria as "0" (not at all) to "3" (nearly every day). It has been validated for use in primary care. It is not a screening tool for depression but it is used to monitor the severity of depression and response to treatment. baseline and 3 months
Secondary Seattle Angina Questionnaire (SAQ) The Seattle Angina Questionnaire (SAQ), developed by Spertus and first reported in the literature in 1994, increasingly is being used to measure cardiac disease-specific quality of life in patients with CAD and baseline and 3 months
Secondary Minnesota Satisfaction Questionnaire (MSQ) The Minnesota Satisfaction Questionnaire (MSQ) is initially designed to measure an employee's satisfaction with his or her job. baseline and 3 months
Secondary Traditional Chinese Medicine (TCM) symptom score scale Traditional Chinese Medicine (TCM) symptom score scale is a score scale for evaluating patients' symptoms from the perspective of TCM. The full score is 30 points, 7-14 points are mild, 15-22 points are moderate and =23 points are severe. baseline and 3 months
Secondary CPET operators-Peak VO2/kg Cardiopulmonary exercise testing ( CPET) is one kind of integrative evaluation of the subject's cardiopulmonary function under a certain exercise load. The information gathered during a CPET is used to calculate Peak VO2 (the highest level of oxygen consumption attained at peak exercise). (ml/kg/min) baseline and 3 months
Secondary CPET operators-metabolic equivalent (METs) In cardiology, and especially when treadmill protocols are used, it is common to express the metabolic requirement for external work as the metabolic equivalent (MET). "MET" is defined as the equivalent of the resting metabolic oxygen requirement. One metabolic equivalent equals 3.5 ml/kg per minute. Exercise capacity (in METS) is a powerful predictor of mortality among men referred for exercise testing. (unit in METs) baseline and 3 months
Secondary CPET operators-peak O2-pulse Another value calculated by CPET is the peak O2-pulse, which indicates how much blood one's heart can pump out with each beat (at the peak level of exercise). (ml/beat) baseline and 3 months
Secondary 6-minute walk distance (6MWD) A 6-minute walk test measures the distance patients can quickly walk in 6 minutes. (in meters) baseline and 3 months
Secondary Exercise compliance-exercise time Exercise time. (in minutes) baseline and 3 months
Secondary Exercise compliance-Exercise frequency Exercise frequency. (per week) baseline and 3 months
Secondary N-terminal pro-brain natriuretic peptide (NT-pro BNP) N-terminal pro-brain natriuretic peptide (NT-pro BNP) in pg/ml baseline and 3 months
Secondary LV end-diastolic volume (LVEDV) The change in echocardiographic measures of ventricular volumes (LV end-diastolic volume). LVEDV in ml. baseline and 3 months
Secondary LV end-systolic volume (LVESV) The change in echocardiographic measures of ventricular volumes (LV end-systolic volume). LVESV in ml. baseline and 3 months
See also
  Status Clinical Trial Phase
Recruiting NCT02793934 - The Pilot Project Development Of MEdical Rehabilitation System in Russian Federation
Recruiting NCT05122455 - Effects of Edoxaban on Platelet Aggregation Phase 2/Phase 3
Completed NCT00289237 - Lifestyle Intervention in a General Population for Prevention of Ischaemic Heart Disease N/A
Completed NCT00331578 - Multi-Center Registry Trial of EXCEL Biodegradable Polymer Drug-Eluting Stent Phase 4
Recruiting NCT05764057 - DAPAgliflozine to Attenuate Cardiac RemOdeling afTEr aCuTe myOcardial Infarction Phase 3
Recruiting NCT04485988 - Influence of Beta Blockers on Prognosis in Patients With Acute Myocardial Infarction Complicated With Normal Ejection Fraction
Terminated NCT00670228 - Effect of Lantus and Apidra in Patients With Acute ST Elevation Myocardial Infarction Phase 3