Condition 1: ??Depression. Condition 2: ??Depression. Condition 3: Anxiety. Condition 4: Breast cancer. Major depressive disorder, single episode, mild Major depressive disorder, single episode, moderate Anxiety disorder, unspecified Carcinoma in situ of breast
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women aged 18 and over Reading and writing literacy in Persian language Interested in participating in a research project Being able to make phone calls and receive SMS Signed written informed consent The use of conventional psychotropic drugs is accepted only if the dosage has been stable for the past 3 months The possibility of using a computer and / or smartphone and the Internet Daily access to the Internet by computer and / or smartphone The ability to participate in research in terms of physical and cognitive Having clinically significant symptoms of mild to moderate anxiety (BAI scores 8 to 25) and/or mild to moderate depression (BDI-S scores 5 to 15)
Exclusion criteria
Exclusion criteria: Significant cognitive impairment or communication problem that affects the ability to provide consent or participate in the study Suffering from other medical diseases and other types of cancer and mental disorders Participating in other interventional research projects at the same time History of participation or intention to participate in an educational workshop that covers the content of the intervention of this research (ACT) Unstable or severe physical or mental conditions Inability to cooperate and give informed consent Having metastatic breast cancer Severe mental illness or disorder or ongoing psychological treatment Inability to use a computer and / or smartphone and the Internet Inability or unwillingness to comply with study requirements Participants who underwent removal of a breast cyst, limited arm and/or shoulder motion, treatment for another type of cancer or diagnosis of another type of cancer, or breast reconstruction Absence of more than one session in intervention group meetings
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Depression score in short form Beck depression inventory. Timepoint: Before the intervention, after the intervention, 4 weeks after the intervention. Method of measurement: Beck depression short inventory.;Anxiety score in Beck anxiety inventory. Timepoint: Before the intervention, after the intervention, 4 weeks after the intervention. Method of measurement: Beck anxiety inventory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ahvaz University of Medical Sciences