Coronary Computed Tomography Angiography
Diagnostic TestIntervention strategies were selected according to CCTA results
NCT Number: NCT05431309
The primary objective of this study is to determine whether coronary computed tomography angiography (CCTA) -based coronary heart disease(CHD) prevention strategy will be superior to traditional CHD prevention strategy, in reducing the future risk of CHD which included myocardial infarction, angina, cardiac death, and an emergency/urgent coronary revascularisation procedure, in a community population aged 40 to 69 years with cardiovascular risk factors but no history of cardiovascular disease.
Trial opening soon.
Get Notified40 year–69 year
All sexes
Interventional
Not applicable
Recent studies found that the incidence of CAD, screening with CCTA, in the general population is as high as 42%~49%. However, the effectiveness of CCTA screening in the primary prevention of CHD is unclear. The investigators designed a randomized controlled, open-label, pragmatic study to determine whether coronary computed tomography angiography (CCTA) -based coronary heart disease(CHD) prevention strategy will be superior to traditional CHD prevention strategy.
Community volunteers aged 40 to 69 years who provide consent, and are eligible (with cardiovascular risk factors but no history of cardiovascular disease), will be randomized 1:1 to receive individualized primary prevention programs for CHD, including statin recommendation, based on CCTA results or traditional risk assessment results using the Chinese guideline on the primary prevention of cardiovascular diseases-recommended strategy. All subjects will be followed for 5 years, but until the target primary endpoint event is met. The primary composite outcome was the first occurrence of CHD, which included myocardial infarction, angina, cardiac death, and an emergency/urgent coronary revascularisation procedure.
In order to prepare the study with high quality, the investigators will performed a pilot study prior to the initiation of patient recruitment for the main study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intervention strategies were selected according to CCTA results
Traditional cardiovascular disease prevention strategy based on Chinese guideline
Time frame: 5 years
Composite of cardiac death, myocardial infarction, angina, and an emergency/urgent coronary revascularisation procedure.
Time frame: 5 years
Number of cardiac death, myocardial infarction, emergency/urgent coronary revascularisation procedure and stroke
Time frame: 5 years
Number of all-cause death, cardiovascular deaths, non-cardiovascular deaths and undetermined death
Time frame: 1 year
Composite outcome: contrast-induced nephropathy and severe allergoid contrast agent reaction
Time frame: 5 years
Number of invasive coronary angiography and coronary revascularisation procedures
Time frame: 5 years
The primary end point(composite of cardiac death, myocardial infarction, angina, and an emergency/urgent coronary revascularisation procedure) will be analyzed in prespecified subgroups, including age, sex, diabetes, smoking status, hypertension, diabetes mellitus, hyperlipidemia, Chronic kidney disease stage 3
Time frame: at 1-year follow-up and final follow-up (5 years)
Measured by Food Frequency Questionnaire
Time frame: at 1-year follow-up and final follow-up (5 years)
Change in activity levels measured through International Physical Activity Questionnaire(IPAQ)
Time frame: at 1-year follow-up and final follow-up (5 years)
Proportion of patients who changed smoking habits (%)
Time frame: at 1-year follow-up and final follow-up (5 years)
Blood pressure(mmHg)
Time frame: at 1-year follow-up and final follow-up (5 years)
Lipids(mmol/L)
Time frame: at 1-year follow-up and final follow-up (5 years)
Body weight(kg)
Time frame: at 1-year follow-up and final follow-up (5 years)
Waist circumference(cm)
Time frame: at 1-year follow-up and final follow-up (5 years)
Change in depression measured using Patient Health Questionnaire-9 (PHQ-9) instrument
Time frame: at 1-year follow-up and final follow-up (5 years)
Change in anxiety measured using Generalized Anxiety Disorder 7-item (GAD-7) instrument
Time frame: at 1-year follow-up and final follow-up (5 years)
Change in quality of sleep measured using Pittsburgh Sleep Quality Index (PSQI) instrument
Time frame: at 1-year follow-up and final follow-up (5 years)
Change in quality of quality of life measured using 12-item Short-Form Health Survey Questionnaire (SF-12) instrument
Time frame: at 1-year follow-up and final follow-up (5 years)
Potential benefits and harms of the findings
Time frame: at 1-year follow-up and final follow-up (5 years)
Measure adherence using follow-up questionnaires (Whether participants are taking medication, why participants are not taking it or taking it, the name, frequency, dosage and side effects of the medication participants are taking)
Time frame: 5 years
Cost-Effectiveness analysis and Cost-Utility analysis
Time frame: 5 years
Radiation dose (mGy-cm)
Contact information is provided by the study sponsor or research team.
Jinling Hospital, China
Other
Role of Screening With Coronary Computed Tomography Angiography in Primary Prevention of Coronary Heart Disease: a Community-based, Prospective Randomised Controlled Study
Acronym: RESPECT
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View the official ClinicalTrials.gov record (opens in a new tab)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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