Condition 1: anxiety disorders. Condition 2: Depression disorders.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age between 18 and 60 years Completion of an informed consent form for participation in the study Ability to read and write Presence of suicidal ideation (obtaining at least one point on the BSSI) Diagnosis of depressive and anxiety disorders based on the SCID-5-CV in accordance with DSM-5-TR criteria No participation in any form of psychotherapy (individual or group) during the past six months No current use and/or no history of alcohol or substance use No history of suicide attempt in the past three months Receiving a stable medication dosage for at least four weeks prior to the start of the intervention, with no changes in the type or dosage of medication during the study period No diagnosis of severe psychiatric disorders such as psychotic disorders or bipolar disorder based on the SCID-5-CV No severe cognitive or neurological disorders such as intellectual disability, dementia, or organic brain disorders that would interfere with effective participation in the intervention
Exclusion criteria
Exclusion criteria: Suicide attempt during the course of treatment Receiving concurrent psychotherapy (individual or group) during treatment Lack of cooperation in completing questionnaires during the study Absence from more than two treatment sessions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of suicidal ideation. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Beck Scale for Suicidal Ideation (BSSI).;Severity of depression. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Beck Depression Inventory-II (BDI-II).;Severity of anxiety. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Beck Anxiety Inventory (BAI). | — |
Secondary
| Measure | Time frame |
|---|---|
| Emotion regulation. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Difficulties in Emotion Regulation Scale – Short Form (DERS-SF).;Rumination. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Ruminative Response Scale (RRS).;Cognitive Flexibility. Timepoint: Before the intervention, immediately after the intervention, and three months after the intervention. Method of measurement: Cognitive Flexibility Inventory (CFI).;Client Satisfaction. Timepoint: Immediately after the intervention and three months after the intervention. Method of measurement: Client Satisfaction Questionnaire (CSQ). | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahid Beheshti University of Medical Sciences