Premenstrual Tension Syndrome
Conditions
Interventions
This is a two-arm, non-randomized, open-label controlled clinical study that will select university women who meet the following inclusion criteria: Being sedentary, with regular menstrual cycles, wit
E02.760.169.063.500.387.875
Sponsors
Universidade Federal do Pará
Programa de Pós Graduação em Ciências do Movimento Humano
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Be woman; university student enrolled in a higher education institution; be between 18 and 50 years of age; have regular menstrual cycles; not be pregnant; not making use of medication for psychological control; does not have pathologies in the reproductive system; does not have musculoskeletal diseases; being sedentary; Premenstrual Syndrome carrier
Exclusion criteria
Exclusion criteria: Do not completely fill out any of the questionnaires given before and during the protocol; absence from training sessions; present pregnancy during the protocol; stop answering the questionnaire, practice other exercises during the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the intensity of premenstrual syndrome symptoms, with maximum score in the symptom intensity questionnaire, between levels 3-4, with the Control Group surpassing the intensity levels of the Resistance Training Group;Evaluate the use of coping strategies, analyzed with the sum of the values of two items, with expected values between 6-8 per domain, with the Resistance Training Group scoring, as the most used domains, those aimed at resolution and adaptation to the problem, compared to the control group | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Countries
Brazil
Contacts
Public ContactEliane Silva
Programa de Pós Graduação em Ciências do Movimento Humano
Outcome results
None listed