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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05654168
Other study ID # Task BIBDIG-6394
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date June 1, 2022
Est. completion date July 1, 2024

Study information

Verified date March 2024
Source Universidad de Murcia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This research will determine the presence of groin pain in professional dancers, through a specific questionnaire on the hip joint. Two groups will be formed made up of dancers over 18 years of age, men and women; one with groin pain and one without groin pain. All participants will undergo a functional muscle ultrasound study, where the thickness of the abdominal muscles, lumbar multifidus and gluteus medius and minor will be evaluated, and the relationship between ultrasound neuromuscular changes and groin pain will be verified


Description:

The objective of the study is to shed light on the to the complexity of the Diagnosis that Groin Pain (GP) encloses, it is proposed to evaluate with Functional Muscular Ultrasonography Rehabilitative Ultrasound Imaging (RUSI), the layer thickness of the gluteal musculature of the hip and the abdominal and lumbar muscles on a sample of professional dancers over 18 years of age with GP to check if there are differences with professional dancers without GP. Expected goals: 1. Identify the presence of GP in professional dancers. 2. To compare the ultrasound characteristics of the neuromuscular system between a sample of dancers with GP and a sample of dancers no GP. 3. Verify the relationship between ultrasound neuromuscular changes with GP.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 25
Est. completion date July 1, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Volunteer Professional dancers 18 years or older, and no maximum age limits Exclusion Criteria: - Not signing the informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Imaging
The thickness of the musculature to be studied will be measured with ultrasonography

Locations

Country Name City State
Spain Miguel Angel Alcocer Ojeda Madrid

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Murcia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other One- Way ANCOVA One-way ANCOVA will used to compare quantitative muscle ultrasound (QMUS) variables in hip with or without groin pain, controlling for effects of clinical covariates Regression models will used to study the relationship between time of evolution (and if necessary, logarithmic transform will applied to this variable to correct the absence of a normal distribution) as independent variable and the QMUS parameters as dependent variables Five months
Primary RUSI. (REHABILITATIVE ULTRASOUND IMAGING) Taking measurements of the layer thickness of abdominal, lumbar and gluteal muscle groups will be performed, with Toshiba's Nemio XG equipment using a multifrequency convex probe from 3 to 6 MGz. Five months
Secondary HAGOS questionnaire Correlate the HAGOS questionnaire with the thicknesses of layer of the different muscle groups analyzed at rest and in contraction in the group with Groin Pain and in the group without Groin pain. Five months
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