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NCT Number: NCT07328789

Factors Influencing Cardiac Rehabilitation Success

Cardiovascular diseases, especially after life-saving surgeries, require comprehensive cardiac rehabilitation (CR). We know that the effectiveness of CR varies among patients. The main goal of this study is to understand which factors-psychological, physical, cognitive, biochemical, and hormonal-influence the success and long-term durability of the recovery process. These findings will help us create more effective and personalized treatment programs.

Who is Being Studied and What is Being Assessed? Study Group: 150 patients of both sexes, aged 50-80 years, hospitalized in the cardiac rehabilitation ward, primarily after Coronary Artery Bypass Grafting (CABG).

Study Period: Patients will be assessed at the start of their hospital stay, at the end of rehabilitation, and again 3-6 months after discharge.

Key Assessment Areas (Modulating Factors)

Physical Status and Fitness:

Exercise tolerance (6-Minute Walk Test).

Muscle strength (handgrip), balance, and gait.

Body composition (analysis of muscle mass and fat tissue).

Respiratory function and diaphragm mobility (ultrasound).

Psychological and Cognitive Factors:

Assessment of anxiety, depression, and general mental well-being.

Evaluation of cognitive functions (memory, concentration) following cardiac surgery.

Sleep Problems (OSA):

Assessment of the risk and severity of Obstructive Sleep Apnea (OSA), which is common in cardiac patients.

Analysis of OSA risk factors related to oral health (dentition, microbiome) and craniofacial structure.

Biological Markers:

Hormonal tests (e.g., testosterone, estradiol) and their correlation with psycho-physical condition and the rehabilitation process.

Analysis of metabolic and muscle-related biomarkers (e.g., myokines: irisin, myostatin).

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Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Observational

About this study

Cardiovascular diseases, particularly advanced coronary artery disease requiring interventions like Coronary Artery Bypass Grafting (CABG), are major global health concerns. Comprehensive cardiac rehabilitation (CR) is a crucial element in patient recovery, yet its effectiveness varies significantly. The main objective of this project is the comprehensive evaluation of the actual effectiveness of standard CR and the identification of multi-faceted factors-biological, functional, and psychosocial-that influence its outcomes and long-term prognosis.

Methodology and Study Design The project plans to recruit 150 male and female patients, aged 50-80 years, who are hospitalized in the cardiac rehabilitation ward, primarily following CABG surgery.

Assessments will be conducted at three key time points to monitor the dynamic nature of changes:

Baseline (T0): At the beginning of cardiac rehabilitation.

Post-Rehab (T1): At the conclusion of the standard rehabilitation program.

Follow-up (T2): Approximately 3-6 months after the patient's discharge.

Detailed Research Domains

The study will focus on several key domains to comprehensively assess the mechanisms underlying recovery:

A. Functional and Physical Assessment

Exercise Tolerance: Measured using the 6-Minute Walk Test (6MWT).

Physical Fitness and Strength: Assessed via Handgrip Dynamometry, the Barthel Scale for daily living activities, and the Tinetti Scale for balance and gait.

Body Composition: Detailed analysis using Bioelectrical Impedance Analysis (BIA) to track changes in muscle mass and fat tissue.

Diaphragm Function: Evaluation of diaphragm muscle thickness and mobility using Ultrasound (USG) to monitor respiratory improvement.

Postural Stability: Assessment of pressure distribution using a tensiometric mat (posturography).

B. Psychological and Neurocognitive Assessment

Mental Status: Evaluated using validated scales, including the WHO-5 Well-Being Index and the HADS Scale for anxiety and depression.

Cognitive Function: Screening for potential post-surgery cognitive impairment (memory, concentration) using the MoCA and MMSE scales.

C. Sleep Disorders and Biological/Hormonal Factors

Obstructive Sleep Apnea (OSA): Objective assessment of the frequency and severity of OSA using a portable sleep monitor.

Oral Health & OSA Risk: Detailed dental and craniofacial examinations to assess OSA risk factors related to the oral cavity status.

Hormonal and Biochemical Markers: Analysis of sex hormones (Testosterone, Estradiol) and their correlation with overall condition and rehabilitation response.

Myokines and Metabolic Signaling: Measurement of myokines (Irisin, Myostatin) and related proteins to understand mechanisms of exercise adaptation.

Standard Laboratory Tests: Including standard markers like lipid profile, glucose, HbA1c, CRP, homocysteine, and Vitamin D3.

Significance and Expected Outcomes The project aims to establish a patient profile that clearly identifies who benefits most from CR and who is at risk of poor outcomes. This identification of predictive factors will enable the early introduction of personalized interventions, such as targeted physical therapy, psychological support, or specialized diagnostics for sleep disorders. The ultimate goal is to optimize CR programs, maximizing gains in physical capacity, quality of life, and the long-term cardiac prognosis for patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male patients aged 50-80 years
  • Hospitalization in the Cardiac Rehabilitation Ward
  • Undergone coronary artery bypass graft (CABG) surgery within the last 30 days
  • Written, informed consent to participate in the study

Exclusion criteria

  • Type II diabetes treated with insulin
  • Neuro-surgical operation in the last 6 months
  • Aneurysms of the cerebral arteries and aorta
  • Recurrent ischemic stroke (Cerebral Vascular Accident)
  • Presence of a pacemaker
  • Current treatment with testosterone

Treatment and study plan

Rehabilitation effective

Other

This study is an observational, non-pharmacological, multi-domain assessment of patients undergoing standard comprehensive cardiac rehabilitation (CR) following CABG surgery. The intervention involves a detailed, longitudinal, three-stage evaluation (Baseline, Post-Rehab, 3-6 Month Follow-up) of the factors influencing CR outcomes.

The CR itself is a standard hospital-based program, but the research intervention is distinguished by its holistic focus on measuring and correlating:

Objective Functional Data: Exercise capacity (6MWT), muscle strength, diaphragm function (USG), and postural stability.

Multifactorial Co-morbidities: Screening for Obstructive Sleep Apnea (OSA) (NOX-T3), Cognitive Dysfunction (MoCA/MMSE), and the role of oral health in OSA risk.

Biological & Hormonal Profile: Measuring Sex Hormones (Testosterone, Estradiol) and Myokines (Irisin, Myostatin) to understand personalized metabolic and adaptive responses to the rehabilitation program.

The intervention aims to

Primary outcomes

  1. Change in Physical Capacity (6MWT)

    Time frame: Baseline (start of hospitalization/T0) and Post-Rehab (end of cardiac rehabilitation/T1, approximately 3-4 weeks later)

    Distance walked in 6 minutes measured in meters using the 6-Minute Walk Test (6MWT). The test reflects objective functional improvement in physical capacity.

Secondary outcomes

  1. Change in Psychological Status (HADS)

    Time frame: Baseline, Post-Rehab (approx. 3-4 weeks later), and Follow-up (3-6 months after discharge

    Assessment using the Hospital Anxiety and Depression Scale (HADS). The scale consists of 14 items (7 for anxiety and 7 for depression). Each item is scored from 0 to 3. Total score for each subscale ranges from 0 to 21. Higher scores indicate greater severity of anxiety or depression.

  2. Diaphragm Thickness

    Time frame: Baseline and Post-Rehab (approx. 3-4 weeks later).

    Assessment of diaphragm muscle thickness measured in millimeters (mm) using Ultrasound (USG) at the end of expiration.

  3. Change in Diaphragm Mobility

    Time frame: Baseline and Post-Rehab (approx. 3-4 weeks later).

    Assessment of diaphragm excursion measured in centimeters (cm) during maximum inspiration and expiration using Ultrasound (USG).

  4. Change in Montreal Cognitive Assessment (MoCA) Score

    Time frame: Baseline, Post-Rehab (approx. 3-4 weeks later), and Follow-up (3-6 months after discharge).

    Cognitive screening using the MoCA scale. Total score ranges from 0 to 30. Higher scores indicate better cognitive function with a score of 26 or above generally considered normal.

  5. Change in Mini-Mental State Examination (MMSE) Score

    Time frame: Baseline, Post-Rehab (approx. 3-4 weeks later), and Follow-up (3-6 months after discharge).

    Cognitive screening using the MMSE scale. Total score ranges from 0 to 30. Higher scores indicate better cognitive function where a score of 24-30 is typically considered normal.

Other outcomes

  1. Change in Apnea-Hypopnea Index (AHI)

    Time frame: Baseline and Post-Rehab (approx. 3-4 weeks later).

    Frequency and severity of Obstructive Sleep Apnea (OSA) events assessed using a portable sleep monitor. The outcome is the number of apneas and hypopneas per hour of sleep (AHI index)

  2. Change in Sex Hormones Concentration

    Time frame: Baseline (fasting) and Post-Rehab (fasting, approx. 3-4 weeks later)

    Serum concentration of Total Testosterone (measured in ng/dL) and Estradiol (measured in pg/mL).

  3. Change in Myokines and Metabolic Markers Concentration

    Time frame: Baseline (fasting) and Post-Rehab (fasting, approx. 3-4 weeks later).

    Serum concentration of Irisin and Myostatin (measured in ng/mL) and other related markers (e.g., PGC-1α, FNDC5, mTOR)

Sponsors and collaborators

Lead sponsor

Pomeranian Medical University Szczecin

Other

Registry information

Official study title

Assessment of the Effectiveness of Comprehensive Cardiac Rehabilitation and Identification of Factors Modulating Its Results

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jan 9, 2026
Registry last updated
Jan 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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