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NCT07544459Completed

Mindfulness-based Stress Reduction Combined With Aerobic Training in Cardiac Rehabilitation After Percutaneous Coronary Intervention: A Dual Impact on Kinesiophobia and Heart Rate Variability

Source: ClinicalTrials.gov · Last updated 22 Apr 2026

Brief summary (registry, in English)

To evaluate the effectiveness of mindfulness-based stress reduction (MBSR) combined with aerobic training on treatment adherence, kinesiophobia, heart rate variability (HRV), exercise tolerance, and psychological stress response in patients with coronary heart disease (CHD) post-percutaneous coronary intervention (PCI). Post-PCI patients (n = 150) were randomly assigned to an observation group (receiving combined MBSR and aerobic training) and a control group (receiving aerobic training only). Treatment adherence, the Tampa Scale for Kinesiophobia-Heart (TSK-SV Heart), HRV parameters, exercise tolerance, and psychological stress responses were assessed before and after the intervention. Psychological assessments included the Self-Rating Anxiety Scale (SAS) and the Self-Rating Depression Scale (SDS).

Status (registry)
Completed
Study type
Interventional
Enrollment
150 (actual)
First submitted
15 Apr 2026
Start date
15 Oct 2023
Primary completion date
17 Jan 2025
Lead sponsor
Linyi People's Hospital
NCT number
NCT07544459

What you commit to

  • Study type: Interventional
  • Participants enrolled: 150
  • From 15 Oct 2023 to the primary completion date, 17 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Coexisting severe organic disease (e.g., severe valvular disease, advanced kidney or liver failure)
    • Malignancy (active or history of cancer within recent years)
    • Cognitive impairment (sufficient to preclude understanding or compliance with mindfulness-based stress reduction or exercise instructions)

Who the study is looking for

  • Confirmed diagnosis of coronary heart disease (CHD)
    • Successful percutaneous coronary intervention (PCI) procedure
    • No contraindications to rehabilitation exercise
    • Provision of written informed consent by the patient and their legal guardian

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Linyi People's Hospital
Coordinator of this site? Confirm its status
LinyiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.