CHD Patient's Concern on Cardiac Rehabilitation

NCT ID: NCT05099692

Last Updated: 2022-05-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

3000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-15

Study Completion Date

2023-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Coronary Heart Disease Cardiac Rehabilitation

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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CHD patients participating in the cardiac rehabilitation

filling out the questionnaire

Intervention Type BEHAVIORAL

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

Interventions

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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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shenyang Northern Hospital

OTHER

Sponsor Role lead

Responsible Party

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Qiang Hu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Qiang Hu

Shenyang, Liaoning, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Qiang Hu, Dr

Role: CONTACT

15291494943

Facility Contacts

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Qiang Hu, Dr

Role: primary

15291494943

Other Identifiers

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N2021-10

Identifier Type: -

Identifier Source: org_study_id

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