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Comparing an Adductor Fatigue Strength Test with Handheld Dynamometry

U

University of Oviedo

Status

Completed

Conditions

Groin Injury
Groin Strain

Treatments

Other: No intervention group.

Study type

Observational

Funder types

Other

Identifiers

NCT06557577
UO2024/01

Details and patient eligibility

About

The strength of the adductor muscles in a population of federated athletes will be measured using two tests: First, the maximum strength test, utilizing handheld dynamometry. Subsequently, endurance strength will be measured with the Adductor Fatigue Test (Brazilian Adductor Performance Test), in order to evaluate a possible correlation between the two tests.

Full description

The strength of the adductor muscles in a population of federated athletes will be measured using two tests: First, the maximum strength test, utilizing dynamometry, where the subject will perform a maximal isometric contraction against the resistance provided by the investigator. Subsequently, endurance strength will be measured with the Adductor Fatigue Test (Brazilian Adductor Performance Test), the participant must perform an adductor exercise as many repetitions as possible until exhaution. In order to evaluate a possible correlation between the two tests and thus, by performing one of them, obtain the results of the other variable.

Apart from the strength measurements, democraphic caracteristics will be recorded to assess possible correlations between studied variables.

Enrollment

150 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Having an active lifestyle
  • Competing at any level in a federated sports discipline.

Exclusion criteria

  • Not consenting to participate in the research.
  • Being unable to understand or write in Spanish.
  • Having sustained any type of injury to the inguinal musculature in the past 3 months.

Trial design

150 participants in 1 patient group

Healthy athletes
Description:
Competitive athletes without any groin injury.
Treatment:
Other: No intervention group.

Trial contacts and locations

1

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Central trial contact

Hugo Olmedillas, PhD

Data sourced from clinicaltrials.gov

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