Remote Balance in Everyday Life for young MI patients with distress
Official title: Evaluation of a Remote Behavioural Stress Recovery Intervention for Myocardial Infarction Patients Younger Than Fifty-five (BRIM-55): A Feasibility Study
Run by Uppsala University · NCT07706816 · Data updated 2026-11-12
This study tests a remote 6-session program (rBEL) to help adults under 55 who had a heart attack and feel distressed see if the program and study procedures are feasible.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 55 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Uppsala University Academic / other |
| Locations | 1 site (Uppsala) |
| Status | Recruiting |
| Started | August 28, 2026 |
| Main results expected | January 31, 2027 |
| Study ends | June 30, 2027 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07706816 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults under 55 with a recent MI (within the past year) who report subjective cardiac distress and can participate remotely.
✕Probably not a fit
Patients without cardiac distress or those with conditions preventing participation may not benefit from the program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This feasibility study enrolls adults under 55 who recently experienced a myocardial infarction and report cardiac distress. Participants complete six remote sessions over 13 weeks to see if the rBEL program can be delivered effectively and if the trial procedures work as planned. It is an uncontrolled, single-arm, pre-post design aimed at informing a future controlled evaluation. Feasibility will be judged against predefined criteria for study procedures and program acceptability. The program uses cognitive behavioral principles to address recovery processes after MI.
Why it matters
Potential benefit: If feasible and acceptable, the approach could lead to a larger study testing whether rBEL helps reduce cardiac distress and improve quality of life.
How similar studies have gone: Previous CBT-based and remotely delivered interventions have shown promise in related cardiac populations, supporting the rationale for exploring rBEL in this group.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria: * Myocardial infarction (MI) before age 55 years * MI within one year prior to randomization * Report of subjective cardiac distress in the initial interview Exclusion criteria: * Serious conditions hindering participation (e.g., active substance misuse, severe mental illness) * Insufficient Swedish proficiency for study procedures, * Disability pension or early retirement at the time of MI
Where it's running
-
Uppsala University
Uppsala, Sweden Recruiting
Study contacts
- Principal investigator: Erik Olsson MG Olsson, Professor — Uppsala University
- Study coordinator: Erik MG Olsson, Professor
- Email: erik.mg.olsson@uu.se
- Phone: +46729999210
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.