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Blended Cardiac Rehabilitation Training for Cardiology Residents

Supervised Hospital-Based Practice Versus Matched Online Activities in Cardiac Rehabilitation Training for Cardiology Residents: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07755878
Acronym
CR-BLEND
Enrollment
98
Registered
2026-08-10
Start date
2025-03-03
Completion date
2026-08-01
Last updated
2026-08-10

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

Conditions

Cardiac Rehabilitation, Medical Education

Keywords

Cardiology residency, Blended learning, Case-based learning, Mini-CEX, DOPS, Cardiopulmonary exercise testing

Brief summary

This randomized controlled trial compares supervised hospital-based practice with matched online activities as part of a common cardiac rehabilitation curriculum for cardiology residents. Ninety-eight residents will be allocated 1:1 to a blended group or an online control group. Both groups will receive the same seven-module online curriculum and the same total scheduled learning time. The blended group will complete a matched block of in-person practice in the cardiology ward, outpatient clinic, and cardiopulmonary exercise testing laboratory, whereas the control group will complete matched-duration supplementary online activities. The primary outcome is the post-training 25-item cardiac rehabilitation knowledge score adjusted for the baseline score. Key secondary outcomes are Mini-CEX and procedure-specific DOPS scores assessed by assessors blinded to allocation.

Detailed description

The curriculum covers cardiac rehabilitation principles; phase I and phase II rehabilitation; cardiopulmonary exercise testing (CPET) and report interpretation; individualized exercise prescription; medication, exercise, nutrition, psychological care, and smoking-cessation prescriptions; multidisciplinary management; patient communication; and management of exercise-related acute events. Both groups receive the same online course, syllabus, learning objectives, and approximately 12 hours of scheduled learning. The blended group replaces one matched-duration block of supplementary online learning with seven supervised in-person sessions. These sessions involve teaching with real patients who provide separate agreement, standardized cases, CPET reports, simulated acute-event scenarios, and immediate feedback. The control group completes additional online case discussions and structured self-study assignments covering the same modules. Measurements occur at three ordered time points. Before randomization and course access, participants complete baseline information and the fixed 25-item knowledge pretest. Immediately after completion of the 7-week course and before release of assessment results, participants complete the same 25-item knowledge post-test and a separate anonymous learner-reported form. Within 7 days after course completion, two independent assessors blinded to allocation complete the Mini-CEX and DOPS ratings. The primary analysis follows the intention-to-treat principle and uses ANCOVA of the post-training knowledge score adjusted for the baseline knowledge score, with multiple imputation for missing baseline or post-training knowledge outcomes.

Interventions

OTHERCommon online cardiac rehabilitation curriculum

A seven-module online course covering cardiac rehabilitation principles, phase I and II rehabilitation, CPET, exercise prescription, the five prescriptions, multidisciplinary care, and acute-event management.

OTHERMatched supplementary online learning

Additional online case discussion and structured self-study assignments covering the same seven modules and matched in scheduled duration to the blended group's in-person sessions.

OTHERHospital-based case and practice sessions

Seven supervised sessions in the cardiology ward, outpatient clinic, and CPET laboratory. Residents practice assessment, risk stratification, CPET interpretation, individualized exercise prescription, patient education, multidisciplinary planning, and simulated acute-event management with immediate instructor feedback.

Sponsors

Second Affiliated Hospital, Zhejiang University, School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

Residents and instructors cannot be blinded to the educational delivery mode. The two Mini-CEX and DOPS examiners do not participate in teaching and are blinded to group allocation.

Intervention model description

Residents are randomized 1:1 to an online control group or a blended learning group. Both groups receive the same online curriculum and matched total scheduled learning time; the matched supplementary block is delivered online in the control group and as supervised hospital-based practice in the blended group.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Resident physician currently participating in standardized residency training * Undertaking a rotation in the Department of Cardiology * Available to attend the cardiac rehabilitation course and study assessments * Provides written informed consent

Exclusion criteria

* Prior systematic cardiac rehabilitation training * Extensive clinical experience in a dedicated cardiac rehabilitation program * Unable to attend the course at the time eligibility is assessed * Declines participation

Design outcomes

Primary

MeasureTime frameDescription
Post-training cardiac rehabilitation knowledge score adjusted for baselineImmediately after completion of the 7-week courseA fixed 25-item multiple-choice examination assesses cardiac rehabilitation fundamentals, phase I rehabilitation, phase II rehabilitation, CPET, exercise prescription, and case-based application. Each correct answer is worth 4 points; total scores range from 0 to 100, with higher scores indicating greater knowledge. The primary estimand is the adjusted between-group difference in the post-training total score from ANCOVA with the baseline total score as a covariate.

Secondary

MeasureTime frameDescription
Mini-Clinical Evaluation Exercise total scoreWithin 7 days after completion of the 7-week courseTwo independent examiners blinded to allocation rate the standard seven Mini-CEX domains: medical interviewing, physical examination, humanistic qualities and professionalism, clinical judgment, counseling and communication, organization and efficiency, and overall clinical competence. Each domain is rated from 1 to 9. Each examiner total ranges from 7 to 63, with higher scores indicating better performance. The analysis score is the mean of the two examiner totals.
Procedure-specific Direct Observation of Procedural Skills total scoreWithin 7 days after completion of the 7-week courseTwo independent examiners blinded to allocation rate 11 items in a standardized CPET-to-exercise-prescription workflow: indications and contraindications, informed consent, preparation, CPET workflow, safety monitoring, termination criteria, report interpretation, exercise prescription, acute-event management, teamwork, and overall procedural competence. Each item is rated from 1 to 9. Each examiner total ranges from 11 to 99, with higher scores indicating better performance. The analysis score is the mean of the two examiner totals.

Countries

China

Contacts

PRINCIPAL_INVESTIGATORYaping Wang

Second Affiliated Hospital, Zhejiang University, School of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026