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Online training to improve health and wellbeing among medical students

Online training to improve health and quality of life among medical students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-104t6bj4
Enrollment
Unknown
Registered
2021-02-19
Start date
2021-02-22
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Depression

Interventions

Eligible medical students will be recruited by email and asked to firstly complete a baseline study survey assessing their sociodemographic and academic characteristics, depressive symptoms (Patient-H
history of suicidal thoughts and attempts, use of medication, presence and history of treatment for mental health disorders
history of trauma before the age of 18 years old (Early Trauma Inventory Self Report – Short Form)
anxiety symptoms (Generalized Anxiety Disorder Questionnaire [GAD-7])
perceived stress (Perceived Stress Scale-10 [PSS-10])
Substance use (Alcohol, Smoking and Substance Involvement Screening Test [ASSIST]
and student engagement (3-item The Utrecht Work Engagement Scale for Students [UWES-S]). The students who complete this web-based survey will be randomized in two groups: experimental group and active
II) Psychoeducation: students read a story about a fictional character, who learned how to use Cognitive-Behavioral Therapy (CBT) skills to deal with stress and mental health is
F04.754.137.350

Sponsors

Escola Paulista de Medicina - Universidade Federal de Sao Paulo
Lead Sponsor
Faculdade de Medicina da Universidade de São Paulo
Collaborator
Faculdade de Medicina do Centro Universitário Estácio de Ribeirão Preto
Collaborator
Faculdade de Medicina de Botucatu da Universidade Estadual Paulista
Collaborator
Faculdade de Medicina da Fundação do ABC
Collaborator
Universidade Federal de São Carlos
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: To be at least 18 years old; to be enrolled in the second academic year of the medical course at one of the seven participating medical schools; to confirmation his/her availability to participate in the intervention phase of the study; to give his/her consent to participate in the study.

Exclusion criteria

Exclusion criteria: Failing to complete the instruments regarding the assessment of depressive symptoms and suicidal thoughts/plans on the database assessment.

Design outcomes

Primary

MeasureTime frame
Change on Patient Health Questionnaire-9 (PHQ-9) depressive symptoms score from baseline to follow-up assessments at 1, 13, and 26 weeks after the intervention) ;Change on item 9 of the Beck Depression Inventory (BDI) score from baseline to follow-up assessments at 1, 13, and 26 weeks after the intervention

Secondary

MeasureTime frame
Change on Generalized Anxiety Disorder Questionnaire -7 (GAD-7) anxiety symptoms score from baseline to follow-up assessments at 1, 13, and 26 weeks after the intervention;Change on Perceived Stress Scale-10 (PSS-10) perceived stress score from baseline to follow-up assessments at 1, 13, and 26 weeks after the intervention;Change on engagement score on the 3-item Utrecht Work Engagement Scale for Students (UWES-S) from baseline to follow-up assessments at 1, 13, and 26 weeks after the intervention

Countries

Brazil

Contacts

Public ContactKarina Pereira-Lima
kplima@unifesp.br+551640420312

Outcome results

None listed

Source: REBEC (via WHO ICTRP)