Comparing the effectiveness of web-based unified transdiagnostic treatment with specific diagnosis

Not Applicable

Recruiting

Conditions: Condition 1: Depression Disorders. Condition 2: Anxiety Disorders. Condition 3: Obsession Compulsive Disorders.

Registration Number: IRCT20110228005931N13

Lead Sponsor: Babol University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 116

Inclusion Criteria

Education above elementary
Vaginal bleeding related to pregnancy between 5 and 12 weeks
Taking progesterone due to the threat of abortion
Internet access
Having diagnostic criteria for disorders, including depression (MDD, depression NOS), anxiety disorders (Panic disorder, Generalized anxiety disorder, Agoraphobia, Specific phobia, Social phobia, and anxiety NOS) and Obsessive-compulsive disorders based on the DSM-5 Clinical Structured Interview

Exclusion Criteria

Patients with vaginal bleeding for reasons other than threatened abortion
Patients who became pregnant through assisted reproductive technology
Patients diagnosed as missed abortion or inevitable miscarriage and ectopic pregnancy on admission
Patients without baseline ultrasound
Severe psychiatric disorders and suicidal ideation
Receiving other psychotherapy at the same time as this study
Lack of informed consent

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depression. Timepoint: Before intervention, after intervention (8 weeks after beginning), fallow-up of 3 month after end of intervention. Method of measurement: Edinburgh Postnatal Depression Inventor.

Secondary Outcome Measures

Name	Time	Method
Anxiety. Timepoint: Before the intervention, after intervention (8 weeks after beginning), fallow-up of 3 months after the end of the intervention. Method of measurement: Brief Symptoms Inventory (BSI-18).;Obsession- compulsion. Timepoint: Before the intervention, after intervention (8 weeks after beginning), follow-up of 3 months after the end of the intervention. Method of measurement: Yale-Brown Obsessive-Compulsive Scale (Y-BOCS).;Emotion regulation. Timepoint: Before intervention, after intervention (8 weeks after beginning), fallow-up of 3 month after end of intervention. Method of measurement: Cognitive emotion regulation questionnaire (CERQ).