The effect of rosemary use in decreasing symptoms of Common Mental Disorders in prison workers and persons deprived of their liberty

INTERVENTION: E02.190 HP3.018 Group of 50 participants, with prison staff and people deprived of liberty of both sexes, divided into 5 groups of 10 people each; received Rosemary capsules in daily doses, for a period of 3 months, of 100mg, 500mg and 1000mg, respectively, being the fourth group of participants who use medication for anxiety and received 500mg, and finally the control group. Before and after the use of herbal medicine, instruments will be applied to assess the presence of common mental disorders, anxiety and musculoskeletal pain in the participants. CONDITION: F03.080 Neurotic Disorders PRIMARY OUTCOME: It is expected to find improvement in anxiety and related outcomes through the method of analysis of the instrument "Beck Anxiety Inventory ‐ BAI". We will observe the sum of the values of all the items, which allows the classification, being a minimum level for scores from 0 to 7 points; light from 8 to 15; moderate from 16 to 25; and record from 26 to 53 points. Data collected before intervention with rosemary extract capsules and after use for three months. SECONDARY OUTCOME: A reduction in pain symptoms is expected, using the Nordic Pain Instrument assessment method. we will observe the results in two moments, before and after the intervention with rosemary extract capsules for three months, with variables from 0 to 4, with 0 being the absence of pain, 1 pain in the last 12 months or 7 days, 2 in the last 12 m and seven days, 3 in the last 12 months or seven days with absence from work, and, 4, for pain in the last 12 months and seven days with absence from work. Level 4 is understood as chronic pain and 1 to 3 non‐chronic pain, zero being the absence of pain. INCLUSION CRITERIA: Be a prison worker for at least one (1) year in one of the prison units that will be the location of this research; person deprived of liberty, with conviction and res judicata; agree to participate by signing the Free and Informed Consent Form