Exercise Adherence of Home-based Cardiac Rehabilitation

July 5, 2021 updated by: Peking University Third Hospital

Qualitative Research on the Influencing Factors of Exercise Adherence of Home-based Cardiac Rehabilitation in Patients With Coronary Artery Disease

The study explored the influencing factors of exercise adherence of home-based cardiac rehabilitation in patients with coronary artery disease.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The study used a qualitative exploratory design. Informants were recruited by purposive sampling. Semi-structured individual interviews were conducted among patients with coronary artery disease and medical professionals in home-based cardiac rehabilitation.

Study Type

Observational

Enrollment (Actual)

26

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Beijing, China, 100191
        • Peking University Third Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 75 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients with coronary artery disease and medical professionals in home-based cardiac rehabilitation

Description

Inclusion Criteria:

  • Diagnosis of coronary artery disease;
  • Age ≤75 years old;
  • Participated in home-based cardiac rehabilitation ≥12 weeks;
  • Have good language skills;
  • Volunteer to participate in this study.

Exclusion Criteria:

  • Have other serious acute or chronic diseases;
  • A previous history of mental illness or a positive family history of mental illness;
  • Have severe audio-visual or speech impairments that may affect understanding and answering questions.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients with coronary artery disease
semi-structured individual interview
medical professionals
semi-structured individual interview

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Influencing factors of exercise adherence
Time Frame: The influencing factors of exercise adherence in home-based cardiac rehabilitation will be measured by the construct of the theory of planned behavior through study completion, an average of 5 months
Influencing factors of exercise adherence in home-based cardiac rehabilitation
The influencing factors of exercise adherence in home-based cardiac rehabilitation will be measured by the construct of the theory of planned behavior through study completion, an average of 5 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Wei Zhao, Peking University Third Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 3, 2020

Primary Completion (Actual)

April 30, 2021

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

June 27, 2021

First Submitted That Met QC Criteria

July 5, 2021

First Posted (Actual)

July 14, 2021

Study Record Updates

Last Update Posted (Actual)

July 14, 2021

Last Update Submitted That Met QC Criteria

July 5, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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