Cognitive-Behavioral and Digital Therapy for Suicide Risk in Eating Disorders
Recruiting
N/A
Interventional Study
Eating Disorders
Suicide Risk
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 150 (estimated)
- Sponsor
- Universitat Autonoma de Barcelona · Other
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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 gr…
Trial Locations
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Eligibility Criteria
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 diagnosi…
Contacts
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