Actively Recruiting
Online Personalized Psychological Intervention for Patients With Heart Disease and Depression or Anxiety (MY-CHOICE)
Led by University of Southern Denmark · Updated on 2026-05-06
30
Participants Needed
3
Research Sites
64 weeks
Total Duration
On this page
Sponsors
U
University of Southern Denmark
Lead Sponsor
A
Aarhus University Hospital Skejby
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Online Personalized Psychological Intervention for Patients With Heart Disease and Depression or Anxiety (MY-CHOICE)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with ischemic heart disease (diagnostic codes I20-I25)
- Referred for cardiac rehabilitation with a positive screen for depression and/or anxiety (HADS score 60 8)
- Access to and ability to use a computer or tablet
- Proficient in the Danish language
You will not qualify if you...
- Severe psychiatric disorders requiring psychiatric care (borderline disorder, schizophrenia, bipolar disorder)
- Severe cognitive difficulties preventing participation (e.g., brain damage, mental retardation, dementia)
- Suicidal thoughts that cannot be managed within the intervention
- Participation in other intervention studies focused on anxiety or depression (unless clinical studies)
- Currently seeing a psychologist or mental health professional for anxiety or depression treatment
- Unable or unwilling to spend 3-4 hours per week on the intervention
- Experiencing significant life stressors that hinder adherence to the treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Aalborg University Hospital, Department of Cardiology
Aalborg, Denmark, 9000
Actively Recruiting
2
Aarhus University Hospital, Department of Cardiology
Aarhus, Denmark, 8200
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3
Zealand University Hospital, Roskilde, Department of Cardiology
Roskilde, Denmark, 4000
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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