Cognitive-Behavioral and Digital Therapy for Suicide Risk in Eating Disorders

Recruiting now · Not applicable

Conditions studied: Eating Disorders, Suicide Risk

In brief

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.

Key facts

Study ID

NCT07417826

Run by

Universitat Autonoma de Barcelona

People needed

150

Starts

2025-10-22

Expected to finish

2028-10-01

Last updated by the study team

2026-02-18

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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).

You may not qualify if…

• 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.

Where it is running

• Hospital Universitari Parc Taulí — Sabadell, Barcelona, Spain (enrolling)

Full record on ClinicalTrials.gov

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