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Clinical Trials/NCT04863677
NCT04863677CompletedNot Applicable

Effect of High-Intensity Interval Training, Moderate Continuous Training, or Guideline-Based Physical Activity on Peak Oxygen Uptake and Myocardial Fibrosis in Patients With Myocardial Infarction: Protocol for a Randomized Controlled Trial

Guangdong Provincial People's Hospital1 site in 1 country188 target enrollmentStarted: May 1, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
188
Locations
1
Primary Endpoint
Evaluate the degree of cardiac fibrosis in 3 groups by cardiac magnetic resonance

Study Overview

Brief Summary

This study will investigate the effect of a 12-weeks cardiac rehabilitation training (HIIT, MICT) program on VO2peak and cardiac fibrosis in patients, and evaluate the effects of HIIT on endothelial function, microvascular obstruction, body fat, inflammation, arrhythmia and psychology .

Detailed Description

Eligible and consenting patients are randomized (block randomization) in a 1:1:1 ratio. According to the number of 180 samples calculated by the sample size, the random number table containing 1-180 ( including shedding cases ) was obtained by the computer. Case number will be assigned to participants in each group according to the order of grouping, and each case number corresponded to Group1(HIIT), 2(MICT) or 3(Control) according to the random number.

The HIIT sessions include brief, intermittent bouts of high-intensity exercise interspersed with periods of low-intensity exercise (active recovery). HIIT include 20 intervals of high-intensity (30-60s at rating of perceived exertion (RPE; Borg scale of 6-20) of 15 to 17) and low-intensity (1min at RPE <10 or totally rest). The whole exercise cycle takes around 40-50 minutes (Figure 2). In MICT Group, patients perform 40-50 minutes at a RPE of 12 to 14(a total of 4 groups, each group 5-8 min, interspersed with 2-minute rest)(Figure 3). HIIT and MICT are performed only during supervised sessions with non-consecutive 3 days/week. And all patients are supervised by professional CR team. After assessing by therapists and doctors, participants also can perform three days of home-based exercises guided by wearing a sports bracelet.

The CR program includes 36 sessions supervised exercises, pharmacological counseling, patient education, catering management, smoking cessation counseling, stress management, and psychological counseling. A standard 36 sessions of CR usually lasts 12 weeks (three sessions per week).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • Aged 18 -75 years
  • Acute myocardial infarction (AMI) patients between 6 weeks and 3 months and had been underwent revascularization, and New York Heart Association functional classification (NYHA) Class I-III; (AMI confirmed by the World Health Organization definition (presence of symptoms of ischemia and changes in electrocardiogram) or the Third Universal Definition of Myocardial Infarction (elevation of a cardiac biomarker along with presence of either symptoms of myocardial infarction or changes in electrocardiogram))
  • Willing and able to attend the complete cardiac rehabilitation(CR)program on their own,assigned the Informed consent form.
  • Complete the cardiopulmonary exercise testing (CPET) at enrollment or has the CPET report within 1 month.

Exclusion Criteria

  • High-intensity exercise frequently
  • Currently participating in any other clinical trials
  • Have any other diseases which limit their life to less than a year (e.g. severe valvular disease, recurrent ventricular arrhythmias, NYHA Class IV heart failure, severe aortic incompetence, severe atrial fibrillation, cancers, and end-stage renal or liver disease)
  • Dementia ; disability or sports contraindication
  • Severe acute liver failure
  • Severe acute renal failure
  • Unstable vital signs
  • Site investigators consider that the patient will be unable to complete the study and/or attend for follow-up.

Arms & Interventions

High Intensity Interval Training(HIIT)

Experimental

The HIIT sessions include brief, intermittent bouts of high-intensity exercise interspersed with periods of low-intensity exercise (active recovery).HIIT include 20 intervals of high-intensity (30-60s at rating of perceived exertion (RPE; Borg scale of 6-20) of 15 to 17) and low-intensity (1min at RPE <10 or totally rest). The whole exercise cycle takes around 40-50 minutes.

Intervention: High Intensity Interval Training(HIIT) (Behavioral)

Moderate Intensity Continuous Training(MICT)

Experimental

Patients perform 40-50 minutes at a RPE of 12 to 14(a total of 4 groups, each group 5-8 min, interspersed with 2-minute rest)

Intervention: Moderate Intensity Continuous Training(MICT) (Behavioral)

Control Group

No Intervention

No additional rehabilitation treatment or physical exercise was added in Control Group.

Outcomes

Primary Outcomes

Evaluate the degree of cardiac fibrosis in 3 groups by cardiac magnetic resonance

Time Frame: 3 months

The effect of HIIT/MICT on myocardial fibrosis in patients with MI, assessed by cardiac magnetic resonance.

The effect of HIIT/MICT on VO2peak

Time Frame: 3 months

Changes in VO2peak after 3-month cardiac rehabilitation training ( HIIT, MICT), assessed by cardiopulmonary exercise testing.

Secondary Outcomes

  • The effect of HIIT/MICT on body circumference(3 months)
  • The effect of HIIT and MICT on depression(Baseline and 3months)
  • The effect of HIIT/MICT on endothelial function as assessed by the Endo-PAT2000(3 months)
  • The effect of HIIT/MICT on quality of life as assessed by SF-36(3 months)
  • The effect of HIIT and MICT on anxiety(Baseline and 3months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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