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Assessment of life habits and health status associated with Fatigue

Phase 4
Recruiting
Conditions
Occupational Stress, fatigue.
C24.580
C23.888.369
Registration Number
RBR-7gfj5r
Lead Sponsor
niversidade Federal de Ouro Preto
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Workers shortlisted for the high performance operator program according to the company's operational technical criteria will be included in the study

Exclusion Criteria

Operators who submit will be excluded:
Evidence of substance abuse or dependence in the last 5 years.
Non-medical psychiatric treatment at least 4 weeks before study.
Clinically significant 24-hour Holter abnormality as complex ventricular arrhythmias, defined as sustained ventricular tachycardia, second-degree mobitz type II or more atrioventricular block, sinus pauses longer than 3 seconds, presence of more than 30 episodes of extrasystoles per hour, and atrial fibrillation or flutter
Decompensated metabolic disorders such as diabetes with glycated hemoglobin (HbA1c) greater than 9% and dyslipidemia with LDL greater than 180 mg / dL or triglycerides greater than 500 mg / dL.
Degenerative chronic diseases (autoimmune, neoplasia, immunodeficient disease and neurological diseases).
Operators with signs and symptoms of infectious diseases.
Gastrointestinal disorders with altered absorption.
Carriers of moderate to severe sleep disorder
Using the following medicines: amitriptyline, clomipramine, imipramine, nortriptyline, fluoxetine, sertraline, paroxetine, venlafaxine, citalopram, lithium carbonate, valproic acid, sodium divalproate, carbamazepine, risperidone, olanzapine, haloperidol, monoaminoxpride inhibitors, moclobemide or selegiline.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It is expected to find a decrease in fatigue prevalence after the intervention verified by applying the Multidimensional Fatigue Inventory 20 (MFI-20) scale and numerical analog scales (NASs) of chronic fatigue symptoms before and after the experiment.
Secondary Outcome Measures
NameTimeMethod
It is expected to find increased quality of life after the intervention verified by applying the World Health Organization Quality of Life-36 (WHOQOL-bref) questionnaire before and after the experiment.
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