Cognitive-Behavioral and Digital Therapy for Suicide Risk in Eating Disorders
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorUniversitat Autonoma de Barcelona
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Cognitive Behavioural Therapy (CBT)
- Cognitive Behavioural Therapy (CBT) + Digital Therapy (DT)
Treatment groups
150 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov