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NCT07706816Recruiting

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

Source: ClinicalTrials.gov · Last updated 7 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
2 Jul 2026
Start date
28 Aug 2026
Primary completion date
31 Jan 2027
Lead sponsor
Uppsala University
NCT number
NCT07706816

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 28 Aug 2026 to the primary completion date, 31 Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Serious conditions hindering participation (e.g., active substance misuse, severe mental illness)

Other

  • Insufficient Swedish proficiency for study procedures,
  • Disability pension or early retirement at the time of MI

Who the study is looking for

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

Age in the registry: 18 years to 55 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
Uppsala University
Coordinator of this site? Confirm its status
UppsalaSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.