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Exercise Support and Rehabilitation for Patients After Spontaneous Coronary Artery Dissection- a Feasibility Study

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The study aims to examine the feasibility of a remote exercise program in women recovering from spontaneous coronary artery dissection (SCAD) events (heart attacks). Heart attacks caused by SCAD are different to the traditional heart attacks. In SCAD a tear happens within the blood vessels causing partial or full blockage. The population affected by SCAD is hugely different to the population affected by other 'traditional' heart attacks; as SCAD mainly happens in otherwise healthy women. From historical cases, SCAD has been associated with strenuous exercise, however, medical research did not find a link. The recovery after SCAD is also very different from other 'traditional' heart attacks. Cardiac rehab programmes are designed for an older population therefore they may not be suitable for a younger predominantly female population. This study will examine if a remote-exercise programme is achievable in people after a SCAD event.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Female

• Aged ≥18 years.

• Diagnosed with angiographically confirmed SCAD and referred to the Leicester SCAD clinic.

• Ejection fraction \>45%.

• Blood pressure \<180/100. Resting heart rate \<100bpm

Locations
Other Locations
United Kingdom
University Hospitals of Leicester
RECRUITING
Leicester
Contact Information
Primary
Noemi Vadaszy, BSc, MSc, PhD
nv96@leicester.ac.uk
+ 44 116 258 3828
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 120
Treatments
Experimental: Exercise Intervention
12 week exercise intervention, + cardiopulmonary exercise test (CPET) + wearable activity monitor for the intervention period
No_intervention: Usual care
Usual car + blinded activity monitor
Related Therapeutic Areas
Sponsors
Leads: University of Leicester
Collaborators: Edinburgh Napier University, University Hospitals, Leicester

This content was sourced from clinicaltrials.gov