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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05099692
Other study ID # N2021-10
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 15, 2021
Est. completion date December 31, 2023

Study information

Verified date April 2022
Source Shenyang Northern Hospital
Contact Qiang Hu, Dr
Phone 15291494943
Email huqiang071@foxmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our study focuses on the question about primary cardiac rehabilitation (CR) patients with coronary heart disease are concerned about demonstrating the association between the patients' view of CR and social associated factors. In our study, all participants are invited to choose at least 1 question in 15 questions or provide their questions regarding their doubt about the CR after filling in their personal information. The selectable questions can be categorized into five titles: the content or purpose of CR, the method of CR, the advantage of CR, the adverse effect of CR, and the expenditure of CR.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age >18 years old - patients diagnosed as coronary heart disease - able to participate in cardiac rehabilitation after medical judgments for the first time - understand the questionnaire content - agree to participant in the study and provide the written informed consent Exclusion Criteria: - unable to complete the questionnaire - patients who aren't willing or refuse to participate in the trial

Study Design


Intervention

Behavioral:
filling out the questionnaire
all participants in our study are invited to choose at least 1 question in 15 questions or provide their own questions regarding their doubt about the CR after filling in their personal information

Locations

Country Name City State
China Qiang Hu Shenyang Liaoning

Sponsors (1)

Lead Sponsor Collaborator
Shenyang Northern Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The total number of different selected questions All participants are invited to choose at least 1 question in 15 questions or provide their questions regarding their doubt about the CR after filling in their personal information. As a result, we calculate and collect the total number of different selected questions for each patients. 5 minutes
Primary The variety of different selected questions All participants are invited to choose at least 1 question in 15 questions or provide their questions regarding their doubt about the CR after filling in their personal information. As a result, we calculate and collect the variety of different selected questions for each patients. 5 minutes
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