Reproducibility of the Functional Movement Screen Test

NCT05535153 | Completed

• 1 other identifier: 20220101
• Study Type: observational
• Target: 61
• Locations: 1 country
• Sites: 1

Brief Summary

The main objective of the study is to determine the inter-evaluator and intra-evaluator reproducibility of the FMS test as an evaluation tool in amateur rugby players. The secondary objective of the study is to evaluate the abilities of the FMS test as a predictive tool for detecting possible injuries during a sports season in amateur rugby players.

Conditions

Locomotor Pain Disorder

Keywords

FMS, rugby

Outcome Measures

Primary Outcomes (1)

• Functional Movement Screen

  Intraclass correlation coefficient with data : FMS score between rater one and rater two

  1 year

Secondary Outcomes (1)

• Functional Movement Screen

  through study completion, an average of 1 year

Study Arms (1)

Experime

Hurdle steps Deep squats Inline lunges Shoulder Clearing Active straight leg raise Trunk stability pushup Rotary stability Spinal extension exam Spinal flexion exam

Other: functional movement screen

Interventions

functional movement screen OTHER

The volunteer subjects had to perform the FMS test at the request of the investigator, which is made up of seven movements: the squat, the crossing of the hurdle, the line lunge, the active elevation with the straight leg, a movement concerning the mobility of the shoulders, a rotational stability assessment movement and a core stability assessment movement.

Experime

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

The subjects recruited are rugby players aged 18 to 55, playing or having played in the "Amateur" and "Senior" categories.

You may qualify if:

• Rugby players in the "Amateur" and "Senior" categories
• Must be able to play a match within a week of the FMS test evaluation.

You may not qualify if:

• players evolving or having evolved beyond the "Federal 3" division for men or "Federal 1" for women
• Pregnant and breastfeeding women
• People in an emergency situation
• People unable to give their consent (including people under guardianship)
• Patients already involved in another study.

Sponsors & Collaborators

• Pole Sante Grace de Dieu: lead

Study Sites (1)

PSLA GDD

Caen, 14000, France

Location

MeSH Terms

Conditions

Collagen Diseases

Condition Hierarchy (Ancestors)

Connective Tissue Diseases; Skin and Connective Tissue Diseases

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: August 16, 2022
• First Posted: September 10, 2022
• Study Start: August 1, 2022
• Primary Completion: May 31, 2023
• Study Completion: May 31, 2023
• Last Updated: September 6, 2023

Record last verified: 2023-09

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)