Under construction – not a live service
Sign in
Taking people in SwedenNo phase

A remote stress recovery program for younger adults after a heart attack

Tests whether an online stress program is workable for adults after a heart attack.

Plain-language title generated from the registry record
Registry title: Evaluation of a Remote Behavioural Stress Recovery Intervention for Myocardial Infarction Patients Younger Than Fifty-five (BRIM-55): A Feasibility Study

Key facts

Where
Uppsala, SwedenSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 55 years old?

Source: NCT07706816, who can take part

Where in Sweden

  • Uppsala UniversityUppsala, SwedenTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Uppsala University
Trial code
NCT07706816
Record updated
7 October 2026
Original description
The goal of this feasibility study is to learn if the randomised controlled trial evaluating the Remote-delivery Balance in Everyday Life (rBEL) programme for adults younger than 55 years who have experienced a myocardial infarction (MI), is feasible.Read full original descriptionShow less

Evaluation of a Remote Behavioural Stress Recovery Intervention for Myocardial Infarction Patients Younger Than Fifty-five (BRIM-55): A Feasibility Study

The goal of this feasibility study is to learn if the randomised controlled trial evaluating the Remote-delivery Balance in Everyday Life (rBEL) programme for adults younger than 55 years who have experienced a myocardial infarction (MI), is feasible.

The objective is to examine the feasibility of the rBEL programme and the associated study procedures before a controlled evaluation of the programme. This is an uncontrolled, single-arm, pre-post treatment designed study.

Participants of the target population will take part of the six session over 13 week programme. Feasibility will be evaluated against predefined feasibility criteria regarding study procedures and programme acceptability.

Inclusion: Myocardial infarction (MI) before age 55 years; MI within one year prior to randomization; Report of subjective cardiac distress in the initial interview.

Exclusion: 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.

ClinicalTrials.gov NCT07706816