Completed
Intraobserver and Interobserver Reproducibility on Hip Clinical Assessment
What is being collected
Data Collection
Who is being recruted
From 18 to 40 Years
+8 Eligibility Criteria
How is the trial designed
Other
Utilizing specific methods not covered by standard models in order to address unique research questions.Observational
Study Start: April 2017
Summary
Principal SponsorFederal University of Rio Grande do Sul
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: April 13, 2017
Actual date on which the first participant was enrolled.Twenty subjects were randomized in two different days: (1) First evaluation of muscle strength, range of motion and single-leg squat performed by the evaluator 1; (2) Repeat the first evaluation with 3 different evaluators
Official TitleIntraobserver and Interobserver Reproducibility on Hip Clinical Assessment
Principal SponsorFederal University of Rio Grande do Sul
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other
Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Criteria
Male
Biological sex of participants that are eligible to enroll.From 18 to 40 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
2 inclusion criteria required to participate
No complaints of pain or knowledge of hip pathology
Subjects willing to enroll
6 exclusion criteria prevent from participating
Subjects reporting that they can not perform the tests due to pain
With previous surgery of the hip or pelvis;
Diabetes Mellitus;
Neuromuscular or neurological diseases;
Show More Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
Exercise Research Laboratory, School of Physical Education, Federal University of Rio Grande do Sul
Porto Alegre, BrazilOpen Exercise Research Laboratory, School of Physical Education, Federal University of Rio Grande do Sul in Google MapsCompletedOne Study Center