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Psychotherapy in Major Depressive Breast Cancer Patients

Comparing the efficacy of group-psychotherapy on breast cancer patients with major depressive disorder who are receiving citalopram

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015063022991N1
Enrollment
40
Registered
2016-01-23
Start date
2015-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Neoplasms. Malignant neoplasm of breast

Interventions

Intervention 1: Control group: citalopram tablets, 20- 40 milligram per day (adjusted based on the patient tolerance and treatment response), for 12 weeks. Intervention 2: Intervention group: Besides
Treatment - Drugs
Behavior
Control group: citalopram tablets, 20- 40 milligram per day (adjusted based on the patient tolerance and treatment response), for 12 weeks
Intervention group: Besides citalopram tablets (20-40 milligram per day) will participate in group cognitive behavioral psychotherapy classes. These group- therapy sessions are held weekly, free in

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Breast cancer in the stage III or more; HADS score equals or more than 11 which can be due to symptomatic major depression; informed consent of the patient for participation in the study Exclusion criteria: severe psychiatric disorders such as psychosis or substance abuse; severe neurologic diseases; mental retardation; endocrine disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: 3th, 6th and 12th weeks. Method of measurement: WHO Quality of Life Questionnaire (WHO-QOL BREF).;Severity of depression in the patient. Timepoint: 3th, 6th and 12th weeks. Method of measurement: Hospital Anxiety and Depression Scale (HADS).

Secondary

MeasureTime frame
The number of suicidal attempts. Timepoint: 3th, 6th and 12th weeks. Method of measurement: self-report questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSussan Moudi

Babol University of Medical Sciences

sussanmo@hotmail.com+98 11 3236 5683

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026