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NCT07569458Recruiting

Online Personalized Psychological Intervention for Patients With Heart Disease and Depression or Anxiety (MY-CHOICE)

Online Personalized and Patient-preferred Comprehensive Intervention for Patients With Heart Disease and Depression or Anxiety (MY-CHOICE)

Source: ClinicalTrials.gov · Last updated 6 May 2026

Brief summary (registry, in English)

The goal of this feasibility study is to assess if the personalised online psychological intervention MY-CHOICE is acceptable to adults with ischemic heart disease and anxiety or depression. It will also examine the reasons for drop-out. The main questions the study aims to answer are: How many participants complete the intervention and what are the reasons for drop-out. And what are the pre-post change scores on anxiety and depression. Participants will: Complete the MY-CHOICE intervention consisting of 6-12 weeks with online modules on various topics based on individual needs in combination with video- or telephone calls with a therapist (psychologist or a trained master student in Psychology) on a need-to basis. Answer a set of questionnaires pre and post intervention. Participate in a brief interview post intervention.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
25 Mar 2026
Start date
4 Jul 2025
Primary completion date
1 Oct 2026
Lead sponsor
University of Southern Denmark
NCT number
NCT07569458

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 4 Jul 2025 to the primary completion date, 1 Oct 2026
  • 3 sites 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

  • Severe psychiatric disorder (i.e., borderline disorder, schizophrenia or bipolar disorder) that requires psychiatric care
  • severe cognitive difficulties (e.g., severe brain damage, mental retardation, or dementia) that will prevent patients from participating

Other

  • endorsement of suicidal ideation with suicidal thoughts (purpose designed questions) that cannot be handled in the intervention
  • participation in other intervention studies focused (unless they are clinical studies)
  • seeing a psychologist or mental health professional for the treatment of anxiety and depression
  • not being able or willing to spend 3-4 hours on the intervention each week
  • experiencing significant life stressors that hinder adherence to the MY-CHOICE treatment

Who the study is looking for

  • ischemic heart disease (diagnostic codes I20-I25),
  • referred for CR with a positive screen for depression and/or anxiety with the Hospital Anxiety and Depression Scale (HADS ≥ 8)
  • access to and ability to use a computer or tablet
  • proficient in the Danish language

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

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Aalborg University Hospital, Department of Cardiology
Coordinator of this site? Confirm its status
AalborgDenmarkRecruiting
Aarhus University Hospital - Department of Cardiology
Coordinator of this site? Confirm its status
AarhusDenmarkRecruiting
Zealand University Hospital, Roskilde, Department of Cardiology
Coordinator of this site? Confirm its status
RoskildeDenmarkRecruiting

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