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

Sponsor
University of Sao Paulo General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05306171
Collaborator
(none)
100
1
2
20.7
4.8

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Online training for healthcare professionals
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effects of Online Training on Self-esteem and Occupational Stress of Healthcare Professionals: a Possible Strategy for Prevention of Burnout Syndrome.
Actual Study Start Date :
Mar 10, 2022
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group (I)

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.

Behavioral: Online training for healthcare professionals
The online training (4 modules) will use the technique of hybrid learning, combining meetings that will require the presence of participants and mediator at the same time and platform (live) with recorded meetings (interviews with experts) that will be watched by the participants at any time (from a distance). Module 1: Self Care; Module 2: Stress and anxiety management; Module 3: Relationships; Module 4: Communication.

No Intervention: Control group (C)

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

Outcome Measures

Primary Outcome Measures

  1. Self esteem [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Rosenberg Self Esteem Scale(RSES)

  2. Occupational Stress [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Stress Questionnaire for Health Professionals (SQHP)

  3. Burnout [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Copenhagen Burnout Inventory(CBI)

Secondary Outcome Measures

  1. Anxiety [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Generalized Anxiety Disorder-7 (GAD-7)

  2. Depression [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Patient Health Questionnaire - 9 (PHQ-9)

  3. Covid-19 impact [Through study completion, an average of 1 year and 4 months]

    Assessed by the instrument Impact of Event Scale - Revised (IES -Rs)

  4. Improvement in general health after entering the study. [Through study completion, an average of 1 year and 2 months]

    Assessed by the instrument Patient Global Improvement Change Scale (PGIC)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Heart Institute of the Hospital das Clínicas, University of São Paulo Medical School São Paulo Brazil 05403-900

Sponsors and Collaborators

  • University of Sao Paulo General Hospital

Investigators

  • Principal Investigator: Patrícia Perniciotti Almeida Costa, Phd student, University of Sao Paulo Medical School

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Carlos Vicente Serrano Jr, Director, University of Sao Paulo General Hospital
ClinicalTrials.gov Identifier:
NCT05306171
Other Study ID Numbers:
  • SDC 4734/18/085
First Posted:
Mar 31, 2022
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Carlos Vicente Serrano Jr, Director, University of Sao Paulo General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2022