anxiety
Conditions
Interventions
This is a randomized, controlled clinical trial with a comparative design involving two treatment groups: participants in the MBRP (Mindfulness-Based Relapse Prevention) – Ser program delivered in a s
Sponsors
Universidade Federal de São Paulo
Universidade Federal de São Paulo
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Be enrolled in an undergraduate or graduate program or be employed at one of the partner universities; have agreed to participate in the study
Exclusion criteria
Exclusion criteria: Have a diagnosis of bipolar disorder; schizophrenia; another severe mental disorder; or a moderate to high risk of suicide; present acute symptoms of depression or anxiety without professional follow-up; have cognitive or sensory or motor impairments that may interfere with participation in the study; have previously engaged in mindfulness meditation within an 8-week structured protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome (attendance count across the eight synchronous sessions, ranging from 0 to 8) will be compared between the Mindfulness-Based Relapse Prevention – Ser online group without the Ser application as supporting material and the Mindfulness-Based Relapse Prevention – Ser online group with the Ser application as supporting material using Student’s t-test with Welch’s correction. The mean difference and its corresponding 95% confidence interval will be estimated. It is expected that the online group receiving support from the supplementary material will attend, on average, 1.5 more sessions compared to the group without the supplementary material | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are anticipated | — |
Countries
Brazil
Contacts
Public ContactLetícia de Oliveira
Universidade Federal de São Paulo
Outcome results
None listed