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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 Record Versions
- This table shows all the versions of this study record arranged in order by submitted date.
- To view one version of the study record, click the submitted date.
- To compare two versions, select them using the check boxes and click “Compare” at the bottom of the list.
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- Data that is changed in the study record is color coded:
- To compare two versions, select them using the check boxes and click “Compare” at the bottom of the list.
| Select | Version | Date submitted (YYYY-MM-DD) | Changes |
|---|---|---|---|
| 1 | 2026-10-14Current |
|
Select two versions to compare.
Viewing V1 (2026-10-14)
Study Details
Study Identification
| Unique Protocol ID | DRAFT-2026-000090 |
|---|---|
| Brief Title | Cardiac rehabilitation via mobile app after myocardial infarction |
| Official Title | A randomized controlled trial of app-delivered cardiac rehabilitation after acute myocardial infarction |
| Secondary IDs |
Study Status
| Record Verification | |
|---|---|
| Overall Status | |
| Study Start | 2026-03-01 |
| Primary Completion | |
| Study Completion | 2027-03-01 |
| First Submitted | 2026-10-14 |
| First Submitted that Met QC Criteria | 2026-09-20 |
| First Posted | 2026-09-20 [Actual] |
| Last Update Submitted that Met QC Criteria | 2026-10-14 |
| Last Update Posted | 2026-10-14 [Actual] |
Sponsor/Collaborators
| Sponsor | Bangladesh Medical University |
|---|---|
| Responsible Party | Bangladesh Medical University |
| Collaborators |
Oversight
| U.S. FDA-regulated Drug | |
|---|---|
| U.S. FDA-regulated Device | |
| Product manufactured in and exported from the U.S. | |
| Data Monitoring |
Study Description
| Brief Summary | |
|---|---|
| Detailed Description |
Conditions
| Condition | Myocardial infarction |
|---|---|
| Keywords |
Study Design
| Study Type | Interventional |
|---|---|
| Primary Purpose | Treatment |
| Study Phase | N/A |
| Interventional Study Model | |
| Number of Arms | 0 |
| Masking | Double blind |
| Allocation | Randomized |
| Enrollment | 300 |
Arms and Interventions
| Arms | Assigned Interventions |
|---|---|
| Device: Mobile cardiac rehabilitation app |
Outcome Measures
| Primary Outcome Measures | Change in peak VO2 at 12 weeks Time Frame: 6 months |
|---|---|
| Secondary Outcome Measures | Adverse events Time Frame: 6 months |
Eligibility
| Minimum Age | |
|---|---|
| Maximum Age | |
| Ages | All ages (Child, Adult, Older Adult) |
| Sex | All |
| Gender-based Eligibility | |
| Gender Eligibility Description | |
| Accepts Healthy Volunteers | |
| 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. |
Contacts/Locations
| Central Contact Person | Dr. Ayesha Rahman +8801700000000 researcher@bmu-ctr.gov.bd |
|---|---|
| Study Officials |
IPD Sharing
| IPD information | Plan to Share IPD: Not provided |
|---|
References
| Citations | |
|---|---|
| Links | |
| Available IPD/Information |
Document Section
| Documents |
|---|