NCT06551532

Brief Summary

The present pilot study aimed to investigate whether a 6-week multicomponent intervention, comprising a structural lumbopelvic and sprint technique program, could reduce anterior pelvic tilt in soccer players who regularly participated in soccer practice.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
17

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 6, 2023

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 8, 2023

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

August 7, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 7, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 13, 2024

Completed
Last Updated

August 13, 2024

Status Verified

August 1, 2024

Enrollment Period

5 months

First QC Date

August 7, 2024

Last Update Submit

August 9, 2024

Conditions

Keywords

Hamstring strainMuscle InjuryPelvic TiltSprint KinematicsSprint Mechanics

Outcome Measures

Primary Outcomes (1)

  • Anterior Pelvic Tilt (APT) Reduction.

    The primary outcome measure is the reduction in static anterior pelvic tilt (APT) immediately after 6 weeks of the multicomponent intervention. APT is measured using a three-dimensional kinematic analysis during static and high-speed running tasks. The reduction in APT will be assessed before (PRE) and immediately after (POST) the intervention period to determine the effectiveness of the intervention in modifying pelvic alignment.

    Baseline (PRE) and immediately after 6 weeks of intervention (POST).

Secondary Outcomes (1)

  • biomechanical variables during high-speed running (HSR) and high-speed soccer running (HSSR) tasks

    Baseline (PRE) and immediately after 6 weeks of intervention (POST).

Study Arms (2)

Multicomponent Intervention Group

EXPERIMENTAL

Soccer players in the intervention group (IG) underwent a multimodal training program comprising 3 sessions per week for 6 weeks. All the soccer players in IG were allowed to continue their usual training (5 sessions per week) and matches (1 per week) at their clubs. The training program comprised both lumbopelvic training (foam rolling, manual therapy, mobility, posture, and strength training) and sprint technique components. The intervention included a total of 18 sessions of approximately 50 minutes each and sessions were supervised by 2 physiotherapists. During the 6 weeks of the intervention, participants performed the multicomponent program 3 times a week. Monday, Wednesday, and Friday were the chosen days for carrying out the training program, as Sunday was usually a game day.

Other: Multicomponent program

Control Group

NO INTERVENTION

Soccer players in the control group (CG) were requested not to modify their established training routines during the entire 6-week period.

Interventions

Lumbopelvic training (foam rolling, manual therapy, mobility, posture, and strength training) and sprint technique program.

Multicomponent Intervention Group

Eligibility Criteria

Age18 Years - 40 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

RX2 Sports and Health

Madrid, 28223, Spain

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
In this study, both participants and researchers are aware of the group assignment. Participants know whether they are receiving the multicomponent intervention or are part of the control group. The researchers who administer the intervention and collect data are also aware of the group assignments.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants are randomly assigned to either an intervention group receiving the multicomponent intervention or a control group with no intervention, with both groups being monitored concurrently throughout the 6-week period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator and PhD Candidate.

Study Record Dates

First Submitted

August 7, 2024

First Posted

August 13, 2024

Study Start

January 6, 2023

Primary Completion

June 8, 2023

Study Completion

August 7, 2024

Last Updated

August 13, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations