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Clinical Trials/RBR-10fg77vk
RBR-10fg77vk
Not yet recruiting
未知

Effects of sliding cupping therapy on pain intensity, fatigue perception and muscular performance after a 10km run

niversidade Federal do Rio Grande do Norte - Faculdade de Ciências da Saúde do Trairí0 sitesJanuary 28, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversidade Federal do Rio Grande do Norte - Faculdade de Ciências da Saúde do Trairí
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 28, 2022
End Date
November 30, 2023
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
niversidade Federal do Rio Grande do Norte - Faculdade de Ciências da Saúde do Trairí

Eligibility Criteria

Inclusion Criteria

  • Street runners for at least 1 year who run twice a
  • week; Being able to run 10 km continuously in the time interval between 40 and 60 minutes in at least one training session; Be between 18 and 45 years old; Not present severe cardiorespiratory or metabolic alterations, proven by a medical report; Not reporting the presence of musculoskeletal disorders in the lower limbs, in the last 6 months, that have prevented the maintenance of the training routine; Do not report any of the contraindications for the application of cupping therapy; Never having used cupping therapy

Exclusion Criteria

  • Presenting disorders in the quadriceps femoris, such as hematoma and cramp, during
  • study procedures; Present allergy or skin irritation due to the use of vegetable oil necessary for cupping therapy; Not being able to complete the 10km run within 60 minutes; Failure to correctly perform the assessment procedures; Not attending any stages of collection development; Make use of anti\-inflammatory drugs, corticosteroids, analgesics or muscle relaxants during the collection period or in the 30 days preceding the beginning of the study; Make use of ergogenic resources, such as anabolic steroids, in the last 6 months prior to the start of collection; Carry out another type of intervention for muscle recovery during the development of the research; Refusing to sign the Free and Informed Consent Form (ICF)

Outcomes

Primary Outcomes

Not specified

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