Feasibility and Process Evaluation of CArdiac Brief INtervention (CABIN) in Patients with ST-Elevation Myocardial Infarction: A Mixed-Method, Pilot Randomised Controlled Trial

Scritto il 27/06/2026
da Gareth Thompson

Eur J Cardiovasc Nurs. 2026 Jun 27:zvag157. doi: 10.1093/eurjcn/zvag157. Online ahead of print.

ABSTRACT

AIMS: To conduct feasibility testing and a process evaluation of CArdiac Brief INtervention (CABIN), with a preliminary assessment of impact in patients with ST-Elevation Myocardial Infarction (STEMI).

METHODS AND RESULTS: A two-arm, parallel group, pilot randomised controlled trial with a concurrent, mixed-method design was conducted. Forty patients were recruited post-STEMI from two hospital centres in the United Kingdom (UK). Participants were randomly assigned to the intervention (CABIN) or control (usual care) group using a 1:1 allocation ratio. CABIN delivered psychoeducational support via a single, one-to-one session (approximately 20 minutes) with patients post-STEMI before hospital discharge. Feasibility and process evaluation data were collected from patients and cardiology staff. Patient-related outcomes were assessed at four timepoints (TPs): baseline, post-intervention, four weeks from diagnosis, and fourteen weeks from diagnosis. The findings demonstrated favourable recruitment (13.3 patients per month), data completeness (≥ 87.5% at each TP), and acceptability (positive feedback with no major revisions identified). Larger, favourable changes (Hedges' g > 0.8) were documented for all patient-related outcomes (disease knowledge; illness perception; anxiety and depression; and health status and confidence) in the intervention group across the TPs. All participants (100%) of the intervention sub-group enrolled in cardiac rehabilitation (CR) compared to 50% of the control sub-group.

CONCLUSION: CABIN was feasible and acceptable to patients. Preliminary evidence suggests a potential, positive impact on disease knowledge, psychological wellbeing, and CR enrolment. CABIN will progress to an effectiveness and implementation evaluation, informing potential integration with routine clinical practice in the UK.

REGISTRATION: ClinicalTrials.gov: NCT05848674.

PMID:42363733 | DOI:10.1093/eurjcn/zvag157