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

Comparison effectiveness of web-based unified transdiagnostic treatment versus diagnosis-specific internet psychotherapies for improvement of psychological distress in women with threatened abortion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110228005931N13
Enrollment
116
Registered
2023-04-13
Start date
2023-04-03
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Interventions

Intervention 1: Intervention group 1: Participants will receive web-based unified transdiagnostic treatment with a duration of 8 weeks, each session 45 minutes. The Unified protocol for transdiagnost
cognitive evaluation in creating and maintaining emotional responses, identifying behaviors affected by emotion, awareness of internal and external triggers of emotion, and learning how to prepare a h

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahbobeh Faramarzi

Babol University of Medical Sciences

Mahbob330@yahoo.com+98 11 3219 9595

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 27, 2026