Depression
Conditions
Interventions
This doctoral project will be executed in two sequential phases. The primary phase endeavors to formulate an unprecedented protocol termed Mindfulness integrated with Cognitive-Procedural Therapy, M-T
Sponsors
Universidade Federal de São Paulo
Universidade Federal de São Paulo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: adults of both sexes; employees; or judges of TRT5; aged 18 years or older; with a score of 7 or more on the SRQ-20. Participants should be able to read, write, and follow instructions and must have internet access
Exclusion criteria
Exclusion criteria: self-declaration of severe symptoms of any mental disorder or ongoing organic disease; having a personality disorder; a diagnosis of schizophrenia; psychotic disorder; suicidal ideation; or drug use causing cognitive impairments in attention and concentration; being in the early stages or adjusting to pharmacological and/or psychotherapeutic treatment; and being a regular practitioner of mindfulness, meditation, or similar practices
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in psychological well-being, assessed by the World Health Organization-Five, WHO-5, which will be applied one week before the intervention, one week after the intervention and at the six-month follow-up | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in depression, assessed by the Patient Health Questionnaire, PHQ-9, which will be applied one week before the intervention, one week after the intervention and at the six-month follow-up.;It is expected to find an improvement in anxiety, assessed by the Generalized Anxiety Disorder Questionnaire, GAD-7, which will be applied one week before the intervention, one week after the intervention and at the six-month follow-up;It is expected to find an improvement in self-care management, assessed by the revised Self-Care Assessment Scale, ASAS-R, which will be applied one week before the intervention, one week after the intervention and at the six-month follow-up | — |
Countries
Brazil
Contacts
Public ContactSara Maria Bitencourt Santos
Universidade Federal de São Paulo
Outcome results
None listed