Musculoskeletal Pain
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. All 27 participants selected for the research will be randomly divided into two groups: Pilates Group, composed of 14 participant
E02.779.474
Sponsors
Universidade Federal de Alfenas
Universidade Federal de Alfenas
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 18 years; men and women; availability of time to carry out the offered protocols; understanding ability
Exclusion criteria
Exclusion criteria: Refusal to receive the protocol; pregnant women; individuals with amputation of one or more limbs; individuals with neurological alterations; not responding to three contact attempts made by the researcher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 2: It is expected to find a decrease in the stress levels of the participants after the treatment period, verified using the Perceived Stress Scale (PSS), from the verification of a variation of at least 5% in pre- and post-intervention measurements.;Expected outcome 1: It is expected to find an increase in the participants' quality of life after the treatment period, verified through the World Health Organization's Quality of Life Instrument questionnaire, synthesized version (WHOQOL-BREF) of the WHOQOL-100 instrument , based on the verification of a variation of at least 5% in the pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 3: It is expected to find a decrease in the presence of painful points in the participants after the treatment period, verified through the Corlett and Manenica Diagram, from the verification of a variation of at least 5% in the pre and post measurements -intervention. | — |
Countries
Brazil
Contacts
Public ContactCamila Rocha
Universidade Federal de Alfenas
Outcome results
None listed