Online Training for Healthcare Professionals: a Possible Strategy for Prevention of Burnout

University of Sao Paulo General Hospital

Status: Unknown

Conditions: Burnout

Treatments: Behavioral: Online training for healthcare professionals

Study type: Interventional

Funder types: Other

Identifiers

NCT05306171

SDC 4734/18/085

Details and patient eligibility

About

This study aims to evaluate the effects of online training on self-esteem and occupational stress of healthcare professionals, in order to evaluate the potential of this intervention as a preventive measure to Burnout syndrome. The study will be developed in three phases,the first being the period of one week before the intervention(t0), when instruments will be first applied.The second phase corresponds to intervention period, when the instruments will be reapplied after the second (t1), third (t2) and fourth (t3) training intervention. The third phase corresponds to the follow up (t4-t8), when all instruments used in the second phase will be reapplied in 2 months (t4), 4 months (t5), 6 months (t6), 8 months (t7) and 12 months (t8) after the end of the intervention.

The sample will consist of 100 health professionals randomized into two groups (50 in each group): intervention group (I), formed by those who will participate in the online training and control group (C), formed by those who will receive the intervention after research is finished.

The hypotheses are: the online training will have greater effect on the increase of self-esteem, and will be identified in health professionals: low levels of global self-esteem, high levels of occupational stress and average levels of burnout.

Enrollment: 100 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Health professionals who work at University of Sao Paulo General Hospital
• Agree and sign the Inform Consent Form.

Exclusion criteria

• Those who, one week before training, presents anxiety and depressive symptoms (GAD ≥ 14 e/ou PHQ ≥ 14)
• in psychotherapy during data collection;
• diagnosed with Burnout syndrome.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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100 participants in 2 patient groups

Intervention group (I)

Experimental group

Description:

Online training for healthcare professionals which will follow a protocol made especially for this research. The online training is composed by 4 modules and each module has 3 meetings. Each meeting has 35 minutes long.

Treatment:

Behavioral: Online training for healthcare professionals

Control group (C)

No Intervention group

Description:

No intervention. The control group will receive the intervention after study is completed.