Overview

The purpose of this study is to determine if adding a digital intervention to standard cognitive-behavioral therapy (CBT) is more effective in preventing suicide risk and reducing eating disorder symptoms. Participants will be women between 18 and 65 years old who have recently experienced suicidal ideation or attempts. One group will receive standard group therapy, while the other will receive group therapy plus a mobile application and digital monitoring devices. The goal is to see if digital tools can improve clinical outcomes and safety for patients.

Eligibility

Inclusion Criteria:

• Gender: Female.
• Age between 18 and 65 years old.
• Clinically stable and able to provide written informed consent.
• Subjects included in the "Suicide Risk Code" (Codi Risc Suïcidi - CRS) program due to recent suicidal ideation or suicide attempts.
• Patients with a diagnosis of an Eating Disorder (ED).

Exclusion Criteria:

• Presence of intellectual disability or cognitive impairment that prevents understanding the therapy or the study requirements.
• Diagnosis of Bipolar Disorder or any Psychotic Disorder.
• Current active substance abuse or dependence.
• Any medical condition that, in the investigator's opinion, makes participation unsafe or unfeasible.