Clinical trial Recruiting at 1 site Interventional Ages 18 to 55

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.

More Anxiety trials

Quick facts

Study typeInterventional
Ages18 Years to 55 Years
SexAll
Enrollment30 (estimated)
SponsorUppsala University
Academic / other
Locations1 site (Uppsala)
StatusRecruiting
StartedAugust 28, 2026
Main results expectedJanuary 31, 2027
Study endsJune 30, 2027
Registry record updatedOctober 7, 2026
Trial IDNCT07706816 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.