RECRUITINGINTERVENTIONAL
Psychosocial Support for Patients With Takotsubo Syndrome
About This Trial
The study hypothesis is that participants enrolled in a virtual Takotsubo support group will have significantly less anxiety at one year.
Who May Be Eligible (Plain English)
Who May Qualify:
\- All patients with documented diagnosis of Takotsubo Syndrome greater than 18 years old.
Who Should NOT Join This Trial:
- 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 willing to sign a consent form will not be included in this research.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
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.
Treatments Being Tested
BEHAVIORAL
Takotsubo Support Group
Participants will undergo virtual group therapy/education. Participants will meet once every other week (at minimum), for 1 - 1.5 hours (on average). The frequency and/or length of the support group sessions may be adjusted according to participants' needs.
Locations (1)
Weill Cornell Medicine
New York, New York, United States