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Clinical Study for Interactive Shared Decision-Making of Drugs for Prevention and Treatment of Coronary Heart Disease

Methods for implementing interactive patient and physician shared decision-making in clinical practice of integrative Chinese and Western medicine

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020234
Enrollment
Unknown
Registered
2018-12-20
Start date
2018-12-31
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary heart disease

Interventions

Group 1:PDA-faciliated Shared decision-making
Group 2:Conventional decision-making

Sponsors

Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) To meet the diagnostic criteria of coronary heart disease; (2) There are stable angina pectoris such as paroxysmal anterior pain and discomfort after exercise, fatigue or emotional excitement, or radiation to the back and left upper limbs for several minutes, rest or disappearance of the above symptoms after taking nitrate drugs; (3) Have decision-making needs, plan to take medicine regularly to prevent and treat angina pectoris attack; (4) Aged35-70 years old; (5) Voluntary signing of informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with infection, fever, trauma, burns, surgical history or active pulmonary tuberculosis or rheumatic immune disease in the past week; (2) Severe arrhythmia (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc.) with hemodynamic changes; (3) Valvular heart disease or primary cardiomyopathy; (4) Patients with acute exacerbation of chronic obstructive pulmonary disease or pulmonary heart disease or respiratory failure; (5) Patients with acute and subacute cerebrovascular diseases; (6) Patients with severe hepatorenal insufficiency, hematological diseases and organ transplantation; (7) Pregnant women and lactating women; (8) Patients with severe mental disorders; (9) Researchers believe that there are other situations that are not suitable for this study.

Design outcomes

Primary

MeasureTime frame
MAPPIN-ODyad;—

Secondary

MeasureTime frame
MAPPIN-QPhysician/Nurse/Patient;Decisional knowledge test;Decision preferance test;Decisional Conflict Scale;—

Countries

China

Contacts

Public ContactMu Wei

Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

muweisonia@foxmail.com+86 13821797520

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026