Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Fibromyalgia
  • Fibromyalgia, Primary
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This is a randomized, single-blinded, parallel, superiority, controlled trial. Participants, women with fibromyalgia, will be allocated to two groups, experimental and control, based on randomization sequence. Sequence will be generated by computer, with 1:1 ratio and blocks of random sizes that are not disclosed to ensure concealment. Allocation concealment will be implemented through a central randomization routine conducted by the same investigator that will generate the sequence. The allocation of participants will occur after the completion of baseline outcomes evaluations.Masking: Single (Outcomes Assessor)Masking Description: Blinding will be implemented for outcome assessor. The questionnaires and functional tests will be supervised remotely by an investigator blinded to the participant's group. Due to the type of interventions, the investigator conducting exercise sessions as well as participants are not blinded.Primary Purpose: Treatment

Participation Requirements

Age
Between 30 years and 60 years
Gender
Only males

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04690400
Collaborators
Not Provided
Investigators
Principal Investigator: Alberton Federal University of Pelotas