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出境医 / 临床实验 / The COmPLETE Study (COmPLETE)

The COmPLETE Study (COmPLETE)

Study Description
Brief Summary:
The project is designed as a large scale, cross-sectional study. This research seeks to identify physical fitness and cardiovascular parameters that best resemble underlying cardiovascular risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure.

Condition or disease Intervention/treatment
Aging Heart Failure Behavioral: Physical Activity

Detailed Description:

Cardiovascular (CV) diseases including heart failure are the leading causes of morbidity, with age being the primary risk factor. The combination of age-related organic functional impairment and reduced physical fitness can drastically impact an individual's healthspan. One's lifespan can potentially be prolonged by the preservation or improvement of physical fitness. However, it remains unclear as to which biomarkers are most suitable for distinguishing between healthy aging and the impaired organ function associated with heart failure. Therefore, a comprehensive assessment of the components of physical fitness and CV function will be performed to identify the most important factors contributing to aging in relation to both health and disease.

This cross-sectional investigation will consist of two parts: the COmPLETE-Health (C-Health) and COmPLETE-Heart (C-Heart) studies. C-Health will examine the aging trajectories of physical fitness components and CV properties in a healthy population sample aged between 20 and 100 years (n = 490). Separately, C-Heart will assess the same markers in patients at different stages of chronic heart failure (n = 80). The primary outcome to determine the difference between C-Health and C-Heart will be cardiorespiratory fitness as measured by cardiopulmonary exercise testing on a bicycle ergometer. Secondary outcomes will include walking speed, balance, isometric strength, peak power, and handgrip strength. Physical activity as a behavioural component will be assessed objectively via accelerometry. Further, CV assessments will include pulse wave velocity; retinal, arterial, and venous diameters; brachial and retinal arterial endothelial function; carotid intima-media thickness; and systolic and diastolic function. The health distances for C-Health and C-Heart will be calculated using the methodology based on statistical (Mahalanobis) distance applied to measurements of quantitative biomarkers.

This research seeks to identify physical fitness and CV biomarkers that best resemble underlying CV risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure. The presented integrative approach could define new recommendations for diagnostic guidance in aging. Ultimately, this study is expected to offer a better understanding of which functional characteristics should be specifically targeted in primary and secondary prevention to achieve an optimal healthspan.

Study Design
Layout table for study information
Study Type : Observational
Actual Enrollment : 678 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Functional Aging in Health and Heart Failure: The COmPLETE Study
Actual Study Start Date : January 3, 2018
Actual Primary Completion Date : December 20, 2019
Actual Study Completion Date : January 31, 2020
Arms and Interventions
Group/Cohort Intervention/treatment
COmPLETE-Health
No intervention
Behavioral: Physical Activity
Physical Activity

COmPLETE-Heart
No intervention
Behavioral: Physical Activity
Physical Activity

Outcome Measures
Primary Outcome Measures :
  1. Cardiorespiratroy Fitness [ Time Frame: 3 hours after inclusion in study ]
    Maximal Oxygen uptake measured by cardiopulmonary exercise testing (VO2peak) in L/min

  2. Ventilatory Efficiency [ Time Frame: 3 hours after inclusion in study ]
    VE/VCO2 measured by cardiopulmonary exercise testing ((L/min)/(L/min))

  3. Oxygen Uptake Efficiency [ Time Frame: 3 hours after inclusion in study ]
    The Oxygen Uptake Efficiency Slope is defined as the regression slope 'a' in V̇O2 = a × log VE +b measured by cardiopulmonary exercise testing.

  4. Gait speed [ Time Frame: 1.5 hours after inclusion in study ]
    Gait speed measured by an inertial sensor system in m/s.

  5. Standing balance [ Time Frame: 2.5 hours after inclusion in study ]
    The cumulative sway path (cm) serves as a measure of postural control.

  6. Hand grip strength [ Time Frame: 2.5 hours after inclusion in study ]
    Measured by a handheld dynamometer. Maximal achieved grip strength (kg) is recorded.

  7. Power of leg muscles [ Time Frame: 2.5 hours after inclusion in study ]
    Peak power measured by countermovement jump performed on a force plate. Reported in N/kg

  8. Arterial stiffness [ Time Frame: 0.5 hours after inclusion in study ]
    Meausred by an noninvasive vascular screening system. Reported as brachial-ankle pulse wave velocity (baPWV).

  9. Endothelial function [ Time Frame: 1 hours after inclusion in study ]
    Meausred as flow mediated dilation (FMD) by ultrasound reported as %.

  10. Left ventricular ejection fraction [ Time Frame: 1 hour after inclusion in study ]
    Meausred by echocardiography reported as %.

  11. Carotid-intima-media thickness [ Time Frame: 1 hour after inclusion in study ]
    Carotid intima-media thickness (mm) is measured by 2D ultrasound instrument.

  12. Retinal arterial and venous diameters [ Time Frame: 7-30 days after inclusion in study ]
    Measured by static retinal vessel analysis. Diameters will be averaged to central retinal arteriolar and venular equivalents (CRAE and CRVE) and the arteriolar-to-venular diameter ratio will be calculated from the CRAE and CRVE.

  13. Retinal endothelial function [ Time Frame: 7-30 days after inclusion in study ]
    Measured by dynamic retinal vessel analysis reported as %.


Biospecimen Retention:   Samples Without DNA
Venous blood samples

Eligibility Criteria
Layout table for eligibility information
Ages Eligible for Study:   20 Years to 100 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

In C-Health, recruitment will be performed until a total number of 490 participants with a valid cardiopulmonary exercise test (CPET) as our primary outcome are included. All participants will be recruited in the area of Basel, including 35 males and 35 females per age category (i.e., 20-29, 30-39, 40-49, 50-59, 60-69, 70-79, and 80+ years of age).

C-Heart will include 80 heart failure patients characterized according to criteria named below.

Stable CHF (treated patient with symptoms and signs that have remained generally unchanged for at least one month) characterized according to the European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure [82], as follows:

  1. HFrEF (LVEF < 40%)
  2. HFmHF (LVEF 40-49%)
  3. HFpEF (LVEF ≥ 50%) and NT-proBNP > 125 pg/mL and structural or functional changes in echocardiography in no. 2 or 3.
Criteria

Inclusion Criteria

C-Health:

• Healthy men and women aged 20-100 years

  • Body mass index < 30 kg/m2
  • Nonsmoker

C-Heart:

  • Stable CHF (treated patient with symptoms and signs that have remained generally unchanged for at least one month) characterized according to the European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure [82], as follows:

    1. HFrEF (LVEF < 40%)
    2. HFmHF (LVEF 40-49%)
    3. HFpEF (LVEF ≥ 50%) and NT-proBNP > 125 pg/mL and structural or functional changes in echocardiography in no. 2 or 3.

      Exclusion criteria

      C-Health:

  • Age younger than 20 years; manifest exercise limiting chronic disease (e.g., myocardial infarction; stroke; heart failure; lower-extremity artery disease; cancer with general symptoms; diabetes; clinically apparent renal failure; severe liver disease; chronic bronchitis GOLD stages II to IV; osteoporosis), women with known pregnancy or breastfeeding; drug or alcohol abuse; hypertonic blood pressure of less than 160/100 mmHg; compromising orthopaedic problems; Alzheimer's disease or any other form of dementia; inability to follow the procedures of the study (e.g., due to language problems, psychological disorders, dementia of the participant); diseases regarded as an absolute contraindication for maximal exertion; and current or past smoking status.

C-Heart:

• Age younger than 20 years; women with known pregnancy or breastfeeding; drug or alcohol abuse; inability to follow the study procedures (e.g., due to language problems, psychological disorders, etc.); unstable angina pectoris; uncontrolled brady- or tachyarrythmia; paroxysmal atrial fibrillation; severe uncorrected valvular disease; acute myocardial infarction or coronary syndrome; transient ischemic attack or stroke occurring less than three months prior; clinically significant concomitant disease states (e.g. uncontrolled hypertonic blood pressure); clinical evidence of current malignancy with exception of basal cell or squamous cell carcinoma of the skin and/or cervical intraepithelial neoplasia; currently receiving systemic chemotherapy and/or radiotherapy; significant musculoskeletal disease other than that associated with heart failure limiting exercise tolerance; active infection; immunosuppressive medical therapy; life-expectancy of less than six months; and prevalence of a disease regarded as an absolute contraindication for maximal exertion.

Contacts and Locations

Locations
Layout table for location information
Switzerland
Department for Sport, Exercise and Health, Section Sports and Exercise Medicine, University of Basel
Basel, Switzerland, 4052
Sponsors and Collaborators
Arno Schmidt-Trucksäss
Tracking Information
First Submitted Date June 5, 2019
First Posted Date June 14, 2019
Last Update Posted Date April 24, 2020
Actual Study Start Date January 3, 2018
Actual Primary Completion Date December 20, 2019   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: June 13, 2019)
  • Cardiorespiratroy Fitness [ Time Frame: 3 hours after inclusion in study ]
    Maximal Oxygen uptake measured by cardiopulmonary exercise testing (VO2peak) in L/min
  • Ventilatory Efficiency [ Time Frame: 3 hours after inclusion in study ]
    VE/VCO2 measured by cardiopulmonary exercise testing ((L/min)/(L/min))
  • Oxygen Uptake Efficiency [ Time Frame: 3 hours after inclusion in study ]
    The Oxygen Uptake Efficiency Slope is defined as the regression slope 'a' in V̇O2 = a × log VE +b measured by cardiopulmonary exercise testing.
  • Gait speed [ Time Frame: 1.5 hours after inclusion in study ]
    Gait speed measured by an inertial sensor system in m/s.
  • Standing balance [ Time Frame: 2.5 hours after inclusion in study ]
    The cumulative sway path (cm) serves as a measure of postural control.
  • Hand grip strength [ Time Frame: 2.5 hours after inclusion in study ]
    Measured by a handheld dynamometer. Maximal achieved grip strength (kg) is recorded.
  • Power of leg muscles [ Time Frame: 2.5 hours after inclusion in study ]
    Peak power measured by countermovement jump performed on a force plate. Reported in N/kg
  • Arterial stiffness [ Time Frame: 0.5 hours after inclusion in study ]
    Meausred by an noninvasive vascular screening system. Reported as brachial-ankle pulse wave velocity (baPWV).
  • Endothelial function [ Time Frame: 1 hours after inclusion in study ]
    Meausred as flow mediated dilation (FMD) by ultrasound reported as %.
  • Left ventricular ejection fraction [ Time Frame: 1 hour after inclusion in study ]
    Meausred by echocardiography reported as %.
  • Carotid-intima-media thickness [ Time Frame: 1 hour after inclusion in study ]
    Carotid intima-media thickness (mm) is measured by 2D ultrasound instrument.
  • Retinal arterial and venous diameters [ Time Frame: 7-30 days after inclusion in study ]
    Measured by static retinal vessel analysis. Diameters will be averaged to central retinal arteriolar and venular equivalents (CRAE and CRVE) and the arteriolar-to-venular diameter ratio will be calculated from the CRAE and CRVE.
  • Retinal endothelial function [ Time Frame: 7-30 days after inclusion in study ]
    Measured by dynamic retinal vessel analysis reported as %.
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title The COmPLETE Study
Official Title Functional Aging in Health and Heart Failure: The COmPLETE Study
Brief Summary The project is designed as a large scale, cross-sectional study. This research seeks to identify physical fitness and cardiovascular parameters that best resemble underlying cardiovascular risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure.
Detailed Description

Cardiovascular (CV) diseases including heart failure are the leading causes of morbidity, with age being the primary risk factor. The combination of age-related organic functional impairment and reduced physical fitness can drastically impact an individual's healthspan. One's lifespan can potentially be prolonged by the preservation or improvement of physical fitness. However, it remains unclear as to which biomarkers are most suitable for distinguishing between healthy aging and the impaired organ function associated with heart failure. Therefore, a comprehensive assessment of the components of physical fitness and CV function will be performed to identify the most important factors contributing to aging in relation to both health and disease.

This cross-sectional investigation will consist of two parts: the COmPLETE-Health (C-Health) and COmPLETE-Heart (C-Heart) studies. C-Health will examine the aging trajectories of physical fitness components and CV properties in a healthy population sample aged between 20 and 100 years (n = 490). Separately, C-Heart will assess the same markers in patients at different stages of chronic heart failure (n = 80). The primary outcome to determine the difference between C-Health and C-Heart will be cardiorespiratory fitness as measured by cardiopulmonary exercise testing on a bicycle ergometer. Secondary outcomes will include walking speed, balance, isometric strength, peak power, and handgrip strength. Physical activity as a behavioural component will be assessed objectively via accelerometry. Further, CV assessments will include pulse wave velocity; retinal, arterial, and venous diameters; brachial and retinal arterial endothelial function; carotid intima-media thickness; and systolic and diastolic function. The health distances for C-Health and C-Heart will be calculated using the methodology based on statistical (Mahalanobis) distance applied to measurements of quantitative biomarkers.

This research seeks to identify physical fitness and CV biomarkers that best resemble underlying CV risk with age. Further, it will examine which physical fitness markers are impaired most in heart failure. The presented integrative approach could define new recommendations for diagnostic guidance in aging. Ultimately, this study is expected to offer a better understanding of which functional characteristics should be specifically targeted in primary and secondary prevention to achieve an optimal healthspan.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Cross-Sectional
Target Follow-Up Duration Not Provided
Biospecimen Retention:   Samples Without DNA
Description:
Venous blood samples
Sampling Method Non-Probability Sample
Study Population

In C-Health, recruitment will be performed until a total number of 490 participants with a valid cardiopulmonary exercise test (CPET) as our primary outcome are included. All participants will be recruited in the area of Basel, including 35 males and 35 females per age category (i.e., 20-29, 30-39, 40-49, 50-59, 60-69, 70-79, and 80+ years of age).

C-Heart will include 80 heart failure patients characterized according to criteria named below.

Stable CHF (treated patient with symptoms and signs that have remained generally unchanged for at least one month) characterized according to the European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure [82], as follows:

  1. HFrEF (LVEF < 40%)
  2. HFmHF (LVEF 40-49%)
  3. HFpEF (LVEF ≥ 50%) and NT-proBNP > 125 pg/mL and structural or functional changes in echocardiography in no. 2 or 3.
Condition
  • Aging
  • Heart Failure
Intervention Behavioral: Physical Activity
Physical Activity
Study Groups/Cohorts
  • COmPLETE-Health
    No intervention
    Intervention: Behavioral: Physical Activity
  • COmPLETE-Heart
    No intervention
    Intervention: Behavioral: Physical Activity
Publications * Streese L, Vaes A, Infanger D, Roth R, Hanssen H. Quantification of Retinal Vessel Myogenic Constriction in Response to Blood Pressure Peaks: Implications for Flicker Light-Induced Dilatation. Front Physiol. 2021 Feb 18;12:608985. doi: 10.3389/fphys.2021.608985. eCollection 2021.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: April 22, 2020)
678
Original Estimated Enrollment
 (submitted: June 13, 2019)
780
Actual Study Completion Date January 31, 2020
Actual Primary Completion Date December 20, 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria

C-Health:

• Healthy men and women aged 20-100 years

  • Body mass index < 30 kg/m2
  • Nonsmoker

C-Heart:

  • Stable CHF (treated patient with symptoms and signs that have remained generally unchanged for at least one month) characterized according to the European Society of Cardiology guidelines for the diagnosis and treatment of acute and chronic heart failure [82], as follows:

    1. HFrEF (LVEF < 40%)
    2. HFmHF (LVEF 40-49%)
    3. HFpEF (LVEF ≥ 50%) and NT-proBNP > 125 pg/mL and structural or functional changes in echocardiography in no. 2 or 3.

      Exclusion criteria

      C-Health:

  • Age younger than 20 years; manifest exercise limiting chronic disease (e.g., myocardial infarction; stroke; heart failure; lower-extremity artery disease; cancer with general symptoms; diabetes; clinically apparent renal failure; severe liver disease; chronic bronchitis GOLD stages II to IV; osteoporosis), women with known pregnancy or breastfeeding; drug or alcohol abuse; hypertonic blood pressure of less than 160/100 mmHg; compromising orthopaedic problems; Alzheimer's disease or any other form of dementia; inability to follow the procedures of the study (e.g., due to language problems, psychological disorders, dementia of the participant); diseases regarded as an absolute contraindication for maximal exertion; and current or past smoking status.

C-Heart:

• Age younger than 20 years; women with known pregnancy or breastfeeding; drug or alcohol abuse; inability to follow the study procedures (e.g., due to language problems, psychological disorders, etc.); unstable angina pectoris; uncontrolled brady- or tachyarrythmia; paroxysmal atrial fibrillation; severe uncorrected valvular disease; acute myocardial infarction or coronary syndrome; transient ischemic attack or stroke occurring less than three months prior; clinically significant concomitant disease states (e.g. uncontrolled hypertonic blood pressure); clinical evidence of current malignancy with exception of basal cell or squamous cell carcinoma of the skin and/or cervical intraepithelial neoplasia; currently receiving systemic chemotherapy and/or radiotherapy; significant musculoskeletal disease other than that associated with heart failure limiting exercise tolerance; active infection; immunosuppressive medical therapy; life-expectancy of less than six months; and prevalence of a disease regarded as an absolute contraindication for maximal exertion.

Sex/Gender
Sexes Eligible for Study: All
Ages 20 Years to 100 Years   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Switzerland
Removed Location Countries  
 
Administrative Information
NCT Number NCT03986892
Other Study ID Numbers 182815
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: No
Responsible Party Arno Schmidt-Trucksäss, University of Basel
Study Sponsor Arno Schmidt-Trucksäss
Collaborators Not Provided
Investigators Not Provided
PRS Account University of Basel
Verification Date April 2020