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Assessment of life habits and health status associated with Fatigue

Fatigue Management Project

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6cs352
Enrollment
Unknown
Registered
2017-10-25
Start date
2016-11-09
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

Men

Interventions

After the screening, the participants were distributed equally among the groups according to changes in the values of waist circumference, LDL, HDL, glucose and blood pressure. 120 participants were i
Dietary supplement
SP6.051.227

Sponsors

Universidade Federal de Ouro Preto
Lead Sponsor
Universidade Federal de Ouro Preto
Collaborator

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: men; adults; alternating shift workers; Vitamin D levels less than 30 ng/mL or less than 75 nmol/L; blood glucose increased; lipid profile increased; blood pressure increased; waist circumference increased

Exclusion criteria

Exclusion criteria: clinical history of malabsorption syndrome, kidney disease, liver or thyroid changes; use of anticonvulsant drugs, steroids, hormones or supplements of vitamins and minerals; altered levels of creatinine, calcium and albumin depending on the kit to be used.

Design outcomes

Primary

MeasureTime frame
The reduction of the prevalence in the 1 year period checked through biochemical analysis from the finding of a difference of at least 18% in the proportion of hypertriglyceridemia in the pre and post intervention measurements

Secondary

MeasureTime frame
Expected outcome 1: The reduction of the prevalence in the 1 year period checked through biochemical analysis from the finding of a difference of at least 36% in the proportion of hypertriglyceridemia in the pre and post intervention measurements with double of the dose administered ;Expected outcome 2: The reduction of the prevalence in the 1 year period checked through biochemical analysis from the finding of a difference of at least 18% in LDL increased proportions in pre and post intervention measurements;Expected outcome 3: The reduction of the prevalence in the 1 year period checked through biochemical analysis from the finding of a difference of at least 18% in abdominal fat increase proportions in pre and post intervention measurements;Expected outcome 4: The reduction of the prevalence of mental fatigue/cognitive deficit in the period of 1 year verified through interviews with cognitive approach in the pre and post intervention measurements

Countries

Brazil

Contacts

Public ContactRaimundo do Nascimento Neto

Universidade Federal de Ouro Preto

ufopraimundo@gmail.com55(31)3559-1060

Outcome results

None listed

Source: REBEC (via WHO ICTRP)