Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05846334

A Mobile Health Intervention Using mindfulHeart to Reduce Stress in Patients with Ischemic Heart Disease

Led by University Hospital, Essen · Updated on 2024-12-24

128

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Essen

Lead Sponsor

U

Universität Duisburg-Essen

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the effects of the mHealth intervention called 'mindfulHeart' on reducing stress in people with ischemic heart disease (IHD). Stress is common in IHD patients and is linked to worse heart health and quality of life. Despite its importance, stress management is not routinely applied in heart care. This trial aims to test how well 'mindfulHeart' works and whether it is a cost-effective way to lower stress in these patients. The intervention 'mindfulHeart' is an interactive, self-guided mobile health program designed to help patients manage stress. It includes automated feedback through visual displays of changes in patient-reported outcomes. Participants use their own internet-enabled smartphones to engage with the program, which is accessible anytime and aims to offer an easy-to-use, scalable option for stress management. Participants will be involved in the study by using the 'mindfulHeart' program and reporting their stress levels and other health outcomes. Researchers will measure overall stress reduction three months after starting the intervention. The study also monitors patients' health-related quality of life and collects data on the cost-effectiveness of this digital approach. The trial includes assessments through questionnaires and continuous tracking of patient-reported outcomes during the study period.

CONDITIONS

Official Title

MHealth Intervention to Reduce Perceived Stress in Patients with Ischemic Heart Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of ischemic heart disease
  • Elevated perceived stress for at least 4 weeks
  • Own an internet-enabled smartphone and know how to use it
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment or communication difficulties affecting study participation
  • Psychiatric or medical conditions requiring alternative treatment
  • No private internet access

AI-Screening

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Trial Site Locations

Total: 1 location

1

Westdeutsches Herz- und Gefäßzentrum, Klinik für Kardiologie und Angiologie

Essen, Germany, 45147

Actively Recruiting

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Research Team

J

Julia Lortz, PD Dr.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

A mHealth intervention to reduce perceived stress in patients with ischemic heart disease: study protocol of the randomized, controlled confirmatory intervention "mStress-IHD" trial.

Julia Lortz, Tienush Rassaf, Christoph Jansen...

https://pubmed.ncbi.nlm.nih.gov/37715203