Burnout Syndrome Clinical Trial
Official title:
Effectiveness of an Intervention for Prevention and Treatment of Burnout in Primary Health Care Professionals
Background: Burnout syndrome is an important health problem that affects many professionals
and must be addressed globally, with both organizational measures and personal
interventions. Burnout of health professionals can be prevented in order to avoid personal,
familial, and social consequences, as well as repercussions for patients.
Methods/Design: This work describes a protocol for a controlled, pragmatic, randomized
clinical trial in 2 parallel groups: intervention and control. All health professionals from
7 health care centers (HCCs) will form the intervention group, and all health professionals
from 7 different HCCs will form the control group. The intervention group will receive 16
hours of training at their work place. The Maslach's burnout inventory (MBI), burnout
physician Questionnaire (CDPM) or burnout nurse Questionnaire (CDPE), and the 28-item
Goldberg's General Health Questionnaire (GHQ-28), validated for our setting, will be used as
measurement tools. Change in the average scores from the MBI emotional exhaustion scale will
be compared between the intervention and control groups, measured as intention-to-treat, and
the intervention will be considered effective if a minimum increase of 20% is achieved.
Discussion: Due to the deleterious consequences of burnout syndrome for people suffering
from it and for the organization where they work, it is necessary to evaluate the
effectiveness of certain interventions for its prevention. Organizational measures are
important for preventing burnout syndrome, but so is providing professionals with coping
strategies, as this group intervention intends to do.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
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