What Are the Effects of Lower Limb Dysmetria on Gluteus Medius and Erector Spinae Musculature?

NCT ID: NCT06217835

Last Updated: 2024-04-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-03-20

Study Completion Date

2023-09-08

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Gluteus Medius (GM) has also been implicated in the development of Low Back Pain (LBP). GM is one of the main pelvic, where he actively participates in control of motion in the frontal and transverse plane, and hip , improving stability to the lumbopelvic-hip complex.

The aim of present study was to investigate whether modifying lower limb length with a different foot insoles of 0.5, 1 and 1.5 cm in a normal population has an effect on ES and GM activity and as a consequence in LBP. As a secondary objective, in turn, to evaluate whether ES and GM activity has an effect on jumping ability as assessed through CMJ.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Background: Length leg discrepancy (LLD), regardless of its origin, is a very common pathology that can contribute to low back pain. Various authors point out its relationship with the lack of activation of both the gluteus medius (GM) and the ipsilateral erector spinae (ES). The purpose of this study was to identify the activation of Es and GM with different simulated LLD, correlating said activation with the LBP. In turn, to evaluate whether ES and GM activity has an effect on jumping ability as assessed through CMJ. (2) Method: a sample of healthy subjects was selected to whom an artificial LLD was incorporated through a 0.5, 1 and 1.5 cm insole, measuring with EMGs in these 3 moments while walking and performing a counter movement jump (CMJ). The measurement was carried out in random order, in terms of insole height, using a Latin Square. Muscle activation patterns were recorded for 30 seconds at each of the insole heights while walking at 5.7 km/h and compared with the maximum voluntary contraction (MVC), both on the ipsilateral and contra-lateral sides. These muscles were then measured under the same circumstances during the development of the CMJ. (3)

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Muscular Disorders, Atrophic

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

0,5 cm jig

A template with the dimensions indicated is introduced to the user and he/she walks for 1 minute.

Group Type EXPERIMENTAL

To evaluate the response of an orthopedic insole

Intervention Type OTHER

To evaluate the response of an orthopedic insole of different heights on gait.

evaluate activation of musculature

Intervention Type OTHER

To evaluate the response caused by an orthopedic insole of different heights on the indicated musculature.

1 cm jig

A template with the dimensions indicated is introduced to the user and he/she walks for 1 minute.

Group Type EXPERIMENTAL

To evaluate the response of an orthopedic insole

Intervention Type OTHER

To evaluate the response of an orthopedic insole of different heights on gait.

evaluate activation of musculature

Intervention Type OTHER

To evaluate the response caused by an orthopedic insole of different heights on the indicated musculature.

1,5 cm jig

A template with the dimensions indicated is introduced to the user and he/she walks for 1 minute.

Group Type EXPERIMENTAL

To evaluate the response of an orthopedic insole

Intervention Type OTHER

To evaluate the response of an orthopedic insole of different heights on gait.

evaluate activation of musculature

Intervention Type OTHER

To evaluate the response caused by an orthopedic insole of different heights on the indicated musculature.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

To evaluate the response of an orthopedic insole

To evaluate the response of an orthopedic insole of different heights on gait.

Intervention Type OTHER

evaluate activation of musculature

To evaluate the response caused by an orthopedic insole of different heights on the indicated musculature.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

\-

Exclusion Criteria

* The volunteers had no problems in range of motion of joints of the lower limbs
* pelvic obliquity due to a functional leg length discrepancy.
* obesity with body mass index (BMI) 35 \> kg/m²
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Camilo Jose Cela University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Eduardo Cimadevilla, PT

Role: STUDY_DIRECTOR

Camilo Jose Cela University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Juan Hernández Lougedo

Villanueva de la Cañada, Madrid, Spain

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Spain

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CamiloJcU-Fisio

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.