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Cardiac rehabilitation via mobile app after myocardial infarction
- BDCTR ID
- BDCTR-2026-000042
- Sponsor
- Bangladesh Medical University
- Information provided by
- Bangladesh Medical University (Responsible Party)
- Last Update Posted
- 2026-10-14
Status not given
No longer looking for participants
Study Overview
Brief Summary
Official Title
Conditions
- Myocardial infarction
Intervention/Treatment
- Device: Mobile cardiac rehabilitation app
Other Study ID Numbers
DRAFT-2026-000090
Study Start
Study Completion
Enrollment
Study Type
Phase
Resource links provided by the National Library of Medicine
Contacts and Locations
This section provides contact details for people who can answer questions about joining this study, and information on where this study is taking place.
To learn more, please see the Contacts and Locations section in How to Read a Study Record.
No location data
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.
For general information about clinical research, read Learn About Studies.
Eligibility Criteria
Inclusion Criteria: Adults aged 18–65 meeting the diagnostic criteria, able to give informed consent. Exclusion Criteria: Pregnancy, severe comorbidity, or inability to attend follow-up.
Ages Eligible for Study
Sexes Eligible for Study
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
- Primary Purpose:
- Treatment
- Allocation:
- Randomized
- Masking:
- Double blind
Arms and Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
Device: Mobile cardiac rehabilitation app |
What is the study measuring?
Primary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
| Change in peak VO2 at 12 weeks | 6 months |
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
| Adverse events | 6 months |
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study Record Dates
These dates track the progress of study record and summary results submissions to the registry. Study records and reported results are reviewed by the Registry Office to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
First Submitted that Met QC Criteria
First Posted
Study Record Updates
Last Update Submitted that Met QC Criteria
Last Update Posted
More Information
Plan for Individual Participant Data (IPD)
Plan to Share Individual Participant Data (IPD)?