PORTHOS - PORTuguese Heart Failure Observational Study

Sponsor
AstraZeneca (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05434923
Collaborator
Sociedade Portuguesa de Cardiologia (Other), NOVA Medical School (Other)
5,616
13
9
432
48

Study Details

Study Description

Brief Summary

This study aims to determine the prevalence of heart failure in the resident population in mainland Portugal aged 50 years or above, using a contemporary, guideline-based diagnostic approach, to optimize patient management and improve strategic healthcare decision-making.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The contemporary prevalence of heart failure in Portugal is largely unknown and may differ from that reported in early studies, which were conducted in the late 1990s-early 2000s with the diagnostic techniques available at the time and did not include neither advanced echocardiographic parameters nor natriuretic peptides measurements. Thus, a large and representative study is needed to address knowledge gaps on the epidemiology, characteristics and burden of heart failure in Portugal. The study aims to determine the prevalence of global heart failure, as well as heart failure subtypes. It also aims to assess the distribution of comorbidities among patients with heart failure, as well as patients' health-related quality of life. The Investigators will conduct a population-based study with a three-stage design approach, enrolling 5616 subjects aged 50 years or above, randomly selected through multi-stage sampling, using the National Health Service as reference: PHASE 0 - Participant selection/enrollment through phone call; PHASE 1 - Screening (NT-proBNP levels determination), health-related quality of life evaluation and sociodemographic characterization; PHASE 2 - Confirmatory assessment with a 12-lead electrocardiography, comprehensive transthoracic echocardiography, extended symptoms assessment and biomarkers assessment; PHASE 3 - Heart failure with preserved ejection fraction exertion testing through a non-invasive echocardiographic diastolic stress test.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    5616 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    PORTHOS - PORTuguese Heart Failure Observational Study: a Nationwide Epidemiological Study on Heart Failure and Asymptomatic Left Ventricle Systolic Dysfunction Based on Contemporary Diagnostic Tools
    Actual Study Start Date :
    Jun 30, 2022
    Anticipated Primary Completion Date :
    Mar 31, 2023
    Anticipated Study Completion Date :
    Mar 31, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of HF among the mainland resident Portuguese population aged 50 or above. [Between March 2022 and March 2023]

      Prevalence of HF among the mainland resident Portuguese population aged 50 or above.

    Secondary Outcome Measures

    1. Age- and gender-specific prevalence of HF among the Portuguese population. [Between March 2022 and March 2023]

      Age- and gender-specific prevalence of HF among the Portuguese population.

    2. Heart Failure reduced Ejection Fraction phenotype prevalence. [Between March 2022 and March 2023]

      Heart Failure reduced Ejection Fraction phenotype prevalence.

    3. Heart Failure mildly reduced Ejection Fraction phenotype prevalence [Between March 2022 and March 2023]

      Heart Failure mildly reduced Ejection Fraction phenotype prevalence

    4. Heart Failure preserved Ejection Fraction phenotype prevalence. [Between March 2022 and March 2023]

      Heart Failure preserved Ejection Fraction phenotypes prevalence.

    5. Prevalence of asymptomatic NT-proBNP elevation. [Between March 2022 and March 2023]

      Prevalence of asymptomatic NT-proBNP elevation.

    6. Prevalence of Pre-HF, as defined by the HF universal definition 2, in patients with asymptomatic NT-proBNP elevation. [Between March 2022 and March 2023]

      Prevalence of Pre-HF, as defined by the HF universal definition 2, in patients with asymptomatic NT-proBNP elevation.

    7. Prevalence of comorbidities among Portuguese HF patients [Between March 2022 and March 2023]

      Prevalence of comorbidities among Portuguese HF patients, namely: CHD, previous MI, hypertension, obesity, DM, VHD, AF, CKD, COPD, OSA;

    8. Prevalence of comorbidities among patients with HFrEF, HFmrEF, and HFpEF phenotypes. [Between March 2022 and March 2023]

      Prevalence of comorbidities among patients with HFrEF, HFmrEF, and HFpEF phenotypes, namely: CHD, previous MI, hypertension, obesity, DM, VHD, AF, CKD, COPD, OSA.

    9. Health-related quality of life 5-level Euro Quality of life-5D version (EQ-5D-5L) [Between March 2022 and March 2023]

      Health-related quality of life 5-level Euro Quality of life-5D version (EQ-5D-5L) consists of 2 pages: the descriptive system (EQ-5D) and the visual analogue scale (EQ VAS). EQ-5D comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression; each one has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the 5 dimensions can be combined into a 5-digit number that describes the patient's health state. The EQ VAS records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' (100) and 'The worst health you can imagine' (0).

    10. Health-related quality of life (Kansas City Cardiomyopathy Questionnaire - KCCQ) [Between March 2022 and March 2023]

      Health-related quality of life (Kansas City Cardiomyopathy Questionnaire - KCCQ). The predictor was the annually updated KCCQ score. The KCCQ is a validated instrument to assess health status among persons with heart failure. The self-administered questionnaire includes 23-items which quantify the importance of dyspnea, fatigue, and edema on physical, social, and emotional functions. The responses are categorized under 3 subscales (symptom burden, physical limitation and quality of life) with a range of possible subscale scores from 0 to 100, with 100 representing the least burden of symptoms. The total KCCQ score represents the mean of the three subscale scores.

    11. Association between health-related quality of life questionnaire (EQ-5D-5L) results and the HF phenotype. [Between March 2022 and March 2023]

      Association between health-related quality of life questionnaire (EQ-5D-5L) results and the HF phenotype.

    12. Association between health-related quality of life questionnaire (KCCQ) results and the HF phenotype. [Between March 2022 and March 2023]

      Association between health-related quality of life questionnaire (KCCQ) results and the HF phenotype.

    Other Outcome Measures

    1. Exploratory Outcome: Association between pre-diabetes and HF prevalence. [Between March 2022 and March 2023]

      Association between pre-diabetes and HF prevalence.

    2. Exploratory Outcome: Association between diabetes mellitus and HF prevalence. [Between March 2022 and March 2023]

      Association between diabetes mellitus and HF prevalence.

    3. Exploratory Outcome: Association between biomarkers of interest (HbA1c%) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (HbA1c%) and HF prevalence.

    4. Exploratory Outcome: Association between biomarkers of interest (serum creatinine) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (serum creatinine) and HF prevalence.

    5. Exploratory Outcome: Association between biomarkers of interest (C-reactive protein) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (C-reactive protein) and HF prevalence.

    6. Exploratory Outcome: Association between biomarkers of interest (troponin) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (troponin) and HF prevalence.

    7. Exploratory Outcome: Association between biomarkers of interest (lipids) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (lipids) and HF prevalence.

    8. Exploratory Outcome: Association between biomarkers of interest (HF biomarkers) and HF prevalence. [Between March 2022 and March 2023]

      Association between biomarkers of interest (HF biomarkers) and HF prevalence.

    9. Exploratory Outcome: Distribution of HF according to geographical area using NUTS II segmentation. [Between March 2022 and March 2023]

      Distribution of HF according to geographical area using NUTS II segmentation.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Community-dwelling citizens living in Mainland Portugal;

    • Registration in a primary care centre;

    • Age ≥50 years at recruitment;

    • Voluntary signed informed consent.

    Exclusion criteria:
    • Living in institutions (e.g., nursing homes, prisons, military facilities, hospitals);

    • Non-Portuguese speakers;

    • Reduced physical and/or cognitive ability hampering participation (e.g., blindness, deafness, or cognitive impairment).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Research Site Aljustrel Portugal
    2 Research Site Aveiro Portugal
    3 Research Site Braga Portugal
    4 Research Site Castelo Branco Portugal
    5 Research Site Coimbra Portugal
    6 Research Site Lagos Portugal
    7 Research Site Lisboa Portugal
    8 Research Site Porto Portugal
    9 Research Site Serpa Portugal
    10 Research Site Setúbal Portugal
    11 Research Site Silves Portugal
    12 Research Site Sobral de Monte Agraço Portugal
    13 Research Site Torres Vedras Portugal

    Sponsors and Collaborators

    • AstraZeneca
    • Sociedade Portuguesa de Cardiologia
    • NOVA Medical School

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    AstraZeneca
    ClinicalTrials.gov Identifier:
    NCT05434923
    Other Study ID Numbers:
    • D1699R00015
    First Posted:
    Jun 28, 2022
    Last Update Posted:
    Aug 11, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by AstraZeneca
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 11, 2022