NCT04344691

Brief Summary

An open-label, single-group, control, pretest-posttest clinical trial is going to be conducted, with 16 healthy sprinters. Rectus femoris length and hamstring strength and electromyography is going to be assessed at baseline, after 10 minutes control and after an static rectus femoris stretching technique. The main objective is to register if an increase in rectus femoris stretching Range of Motion, increases hamstring strength and activity due to their antagonic relationship and their relation with pelvic tilt.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
16

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2020

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 15, 2020

Completed
10 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 25, 2020

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 7, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 14, 2020

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2020

Completed
Last Updated

April 16, 2020

Status Verified

April 1, 2020

Enrollment Period

10 days

First QC Date

April 7, 2020

Last Update Submit

April 14, 2020

Conditions

Keywords

muscle lengthstrengthsprint

Outcome Measures

Primary Outcomes (3)

  • Rectus femoris length

    Knee flexion range of motion with inclinometer

    Inmediate after intervention; up to 10 minutes

  • Biceps femoris strength

    Dynamometry

    Inmediate after intervention; up to 10 minutes

  • Gluteus maximus strength

    Dynamometry

    Inmediate after intervention; up to 10 minutes

Secondary Outcomes (3)

  • Rectus femoris tensomyography

    Inmediate after intervention; up to 10 minutes

  • Pelvic anteversion

    Inmediate after intervention; up to 10 minutes

  • Sprint muscle activity

    Inmediate after intervention; up to 10 minutes

Study Arms (2)

Control

NO INTERVENTION

5 minutes waiting time

Stretching

EXPERIMENTAL

Rectus femoris static stretching during 90' (with three hold-relax progressions until final ROM)

Procedure: Rectus femoris stretching

Interventions

Patient lying prone with the non-implicated leg outside the treatment table resting on the floor. Physical therapist flexes patients knee until tension is felt. In that position 5 seconds' isometric contraction is asked and physical therapist progresses in knee flexion range of motion until new tension is felt. After three contract-relax procedures physical therapist holds the range of motion for 30 seconds.

Stretching

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • The athletes recruited have to be under regular training and competition
  • Free of any symptoms, at least 3 days training weekly for the last three years
  • Give written consent

You may not qualify if:

  • \- Subjects who have suffered lower limb or back injuries during those last three years

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cnetro ragonés del Deporte

Zaragoza, 50018, Spain

Location

Study Officials

  • Alazne Ruiz de Escudero Zapico, PhD

    Universidad Pública de Navarra

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 7, 2020

First Posted

April 14, 2020

Study Start

February 15, 2020

Primary Completion

February 25, 2020

Study Completion

April 30, 2020

Last Updated

April 16, 2020

Record last verified: 2020-04

Data Sharing

IPD Sharing
Will share

All individual participant data that underlie results in a publication

Shared Documents
SAP, ICF, CSR
Time Frame
Starting 6 months after publication
Access Criteria
Principal investigator will review requests and criteria for reviewing requests will be individually assessed

Locations