Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05846334

MHealth Intervention to Reduce Perceived 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

Stress is highly prevalent in patients with ischemic heart disease (IHD) and is associated with lower health-related quality of life and worsened cardiovascular outcome. The importance of stress management is now recognized in recent cardiovascular guidelines. However, effective stress management intervention are not implemented in clinical routine yet. The development of easily disseminated eHealth interventions, particularly mHealth, may offer a cost-effective and scalable solution to this problem. The aim of the proposed trial is to assess the efficiency and cost-effectiveness of the mHealth intervention 'mindfulHeart' in terms of reducing stress in patients with IHD.

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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.

CONTACT

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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