Evaluation of the Action of Cuction Therapy in the process of non-specific Pai

Not Applicable

Recruiting

• Conditions: pain; backache; joint pain; C23.888.592.612

• Registration Number: RBR-6qswsj2
• Lead Sponsor: niversidade de Franca

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-10-08
• Study Completion: 2022-02-28
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

The research participant must be included in the age group from 18 to 60 years old, regardless of gender, who present acute or chronic muscle pain.

Exclusion Criteria

The participant will be excluded from the research when presenting any of the following pathologies: (1) cancer, (2) chronic kidney disease, (3) coagulopathies, (4) thrombopathologies and (5) hemodynamic and vascular changes. Such exclusion occurs from the literature, as cupping therapy process can exacerbate such pathological participants.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The reduction of self-reported pain assessed at the beginning of the intervention by means of a visual analogue scale is expected as the primary outcome.

Secondary Outcome Measures

Name	Time	Method
Improvement of the individual's functional quality is expected within the secondary outcome, through the analysis of the adapted Q-Adom scale, in which the participant will respond within 24 hours after the cupping technique, thus identifying changes in the pattern of sleep, emotional state, modification of daily habits.