Virtual support group for patients with Takotsubo syndrome
Psychosocial Support for Patients With Takotsubo Syndrome
This study is testing if joining a virtual support group can help adults with Takotsubo syndrome feel less anxious after a year.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 24 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Weill Medical College of Cornell University Academic / other |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT05977049 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of a virtual support group for individuals diagnosed with Takotsubo syndrome, also known as broken heart syndrome. The hypothesis is that participation in this support group will lead to a significant reduction in anxiety levels after one year. Takotsubo syndrome often presents with symptoms similar to a heart attack and can be triggered by intense emotional or physical stress. The study will include patients over 18 years old who have a documented diagnosis of Takotsubo syndrome, while excluding those already receiving psychotherapy or unable to provide informed consent.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 with a documented diagnosis of Takotsubo syndrome.
Not a fit: Patients currently undergoing psychotherapy or those unable to provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce anxiety and improve the quality of life for patients suffering from Takotsubo syndrome.
How similar studies have performed: While there have been studies on psychosocial support in other cardiac conditions, this specific approach for Takotsubo syndrome is relatively novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- All patients with documented diagnosis of Takotsubo Syndrome greater than 18 years old. Exclusion Criteria: * Patients with a diagnosis of Takotsubo Syndrome already undergoing Psychotherapy or those who choose not to participate. * Vulnerable populations such as prisoners, non-English speaking subjects, pregnant women, and subjects unable to provide written informed consent will not be included in this research.
Where this trial is running
New York, New York
- Weill Cornell Medicine — New York, New York, United States (Recruiting)
Study contacts
- Principal investigator: Jim Cheung, MD — Weill Medical College of Cornell University
- Study coordinator: Heather Glum, BSN, MPA
- Email: hep2011@med.cornell.edu
- Phone: 212-746-4617
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.