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Clinical Trials/NCT06239246
NCT06239246
Completed
Not Applicable

Analyzing the Association Between Cardiovascular Diseases and Mental Illness Considering Environmental Risk Factors

Ningbo No. 1 Hospital2 sites in 1 country400 target enrollmentOctober 1, 2022

Overview

Phase
Not Applicable
Intervention
Behavioral
Conditions
Cardiovascular Diseases
Sponsor
Ningbo No. 1 Hospital
Enrollment
400
Locations
2
Primary Endpoint
severity of depressive symptoms through CES-D
Status
Completed
Last Updated
19 days ago

Overview

Brief Summary

Cardiovascular diseases (CVD) are important public health concerns around the world and closely associated with the development and progression of mental illness, which in turn increases the risk of developing cardiovascular diseases. This study aimed (1) to explore the known or unknown protective and risk factors underlying this comorbidity using questionnaires; (2) to study the biomarkers (body fluid, imaging) of the participants, and to find the influence on the relationship between CVD and mental health; (3) to identify high-risk populations for mental disorders in CVD patients and to establish prediction models. (4) to establish a specialized medical database.

Detailed Description

Patients with depression and cardiovascular comorbidities have a worse prognosis, a sharply reduced quality of life, and a much higher incidence of fatal CVD events, such as acute infarction, than patients with a single disease. However, due to the variety of potential causative factors and clinical manifestations, population variability, long duration of the disease, as well as neurological disorders of the exact causative mechanism still unclear, the psychological assessment among patients with cardiovascular diseases is remarkably inadequate studied. In this study, two cohorts are established that include 2000 hospitalized patients and 5000 of the entire population. All individuals are screened for depression and anxiety. Those who score positive will be advised to enroll in this study. Patients are then randomized to receive collaborative care involving the patient, the patient's primary care physician, cardiologist and nurse case manager, or usual care is defined for each patient. Whole blood and serum samples are obtained from all patients, which will be measured for a panel of metabolic and inflammatory indicators. Patients in both cohorts will be monitored for depression severity and duration at 6 and 12 months after enrollment. A statistical technique is applied to determine the effect size of potential risk factors.

Registry
clinicaltrials.gov
Start Date
October 1, 2022
End Date
December 25, 2025
Last Updated
19 days ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Ningbo No. 1 Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Outpatient and inpatient cardiology patients, diagnosed with at least one cardiovascular disease and at least one psychological disorder
  • Cardiovascular diseases: ACS (STEMI, non-STEMI, unstable angina), arrhythmia (atrial fibrillation, atrioventricular block), heart failure (stable/unstable), hypertension, cardiomyopathy (hypertrophic, dilated)
  • Psychological disorders: structured interview diagnosed as depression, anxiety, insomnia; PHQ-9/GAD-7 score ≥ 10 points.
  • 4.18-70 years old

Exclusion Criteria

  • Clear suicidal ideation: PHQ-9 item 9 suicide ideation ≥ 3 points
  • Severe mental illnesses such as bipolar disorder, schizophrenia
  • Currently under psychotherapy
  • Severe cardiovascular diseases or other severe chronic life-threatening diseases
  • Refusal to participate
  • Abuse of alcoholism and drugs
  • Pregnant or breastfeeding
  • Cognitive impairment

Arms & Interventions

2000 hospitalized patients

hospitalized patients with heart diseases

Intervention: Behavioral

10000 community population

Outcomes

Primary Outcomes

severity of depressive symptoms through CES-D

Time Frame: cross-sectional analyses in 2024

severity of depressive symptoms through CES-D Include 20 questions, sum all points. Total points 60. Judgment critaria: ≤15 as no depressive symptoms, 16-19 as possible depressive symptoms, ≥20 as definite depressive symptoms.

7-item Generalized Anxiety Disorder scale (GAD-7)

Time Frame: cross-sectional analyses in 2024

Total points 21. Anxiety judgment criteria: 0-4 as no, 5-9 as mild, 10-14 as moderate, 15-21 as severe.

The Patient Health Questionnaire 9-item depression scale (PHQ-9)

Time Frame: cross-sectional analyses in 2024

Total points 27. depression judgment criteria: 0-4 as no, 5-9 as mild, 10-14 as moderate, 15-19 as moderate to severe, 20-27 as severe. Framingham risk score,NYHA cardiac function classification, six-minute walk test

Six-minute walk test

Time Frame: cross-sectional analyses in 2024

A 6-minute walking distance of less than 150 meters indicates severe heart failure, 150-450 meters indicates moderate heart failure, and\>450 meters indicates mild heart failure.

Pittsburgh sleep quality index,PSQI

Time Frame: cross-sectional analyses in 2024

Include 23 items. Total points 21. Sleep quality judgment criteria: 0-5 very good, 6-10 good, 11-15 fair, 16-21 poor.

New York heart failure classification

Time Frame: cross-sectional analyses in 2024

Judgment criteria: Class I: patients are not limited in daily activities; Class II: patients are mildly limited in physical activity; Class III: patients are significantly limited in physical activity; Class IV: patients can not be engaged in any physical activity.

Secondary Outcomes

  • Major Adverse Cardiac Events(24 months)

Study Sites (2)

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