Immediate Impact of Lumbar Fascia Stretching on Hamstring Flexibility

April 9, 2020 updated by: David Perez Cruzado, Universidad Católica San Antonio de Murcia

Immediate Impact of Lumbar Fascia Stretching on Hamstring Flexibility: a Randomized Clinical Trial

Introduction: the hamstring muscles has a great tendency to decrease its extensibility, originating a pathology with a own clinical entity, the Short Hamstring Syndrome (SHS), in addition to other problems on adjacent structures. All this present a great socioeconomic impact in the investigator's society. Various techniques have been demostrated to prduce an increase in flexibility, among which are the fascial techniques.

Objective: to evaluate the immediate efficacy of the treatment of the lumbar fascia in the flexibility of the hamstring musculature.

Methods: 41 women between 18 and 39 years old, in two groups. The experimental group received a technique of fascial stretching in the lumbar area while the control group participated in an off magnetotherapy machine. The hamstring flexibility in both lower limbs was measured by the Straight Leg Raising Test (SLR) and the Passive Popliteal Angle Test (PKE).

Study Overview

Detailed Description

The hamstring muscles has a great tendency to decrease its extensibility, originating a pathology with a own clinical entity, the Short Hamstring Syndrome (SHS), in addition to other problems on adjacent structures. This study aims to help improve treatment for the problem mentioned before, which can be included within a therapeutic framework to combat SHS. In recent years, investigations have been carried out that include different techniques for stretching the hamstring muscles, as well as the treatment of other structures belonging to the posterior superficial chain. Within this last section, myofascial stretching techniques have been shown to be effective both in the short and medium term. Different techniques for stretching the hamstring muscles have been carried out with the aim of increasing the flexibility of the lower back in general.

he objective is to evaluate the immediate efficacy of the treatment of the lumbar fascia in the flexibility of the hamstring musculature.

The participants are 41 women between 18 and 39 years old, in two groups. The experimental group received a technique of fascial stretching in the lumbar area while the control group participated in an off magnetotherapy machine. The hamstring flexibility in both lower limbs was measured by the Straight Leg Raising Test (SLR) and the Passive Popliteal Angle Test (PKE).

Study Type

Interventional

Enrollment (Actual)

41

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Murcia, Spain, 30107
        • Universidad Católica San Antonio de Murcia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 39 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Female between 18 and 39 years old.
  • Signed informed consent

Exclusion Criteria:

  • Any alteration that prevents the normal communication between the patient and the therapist at the time of the study.
  • Have an injury in the hamstring muscles.
  • Have a chronic or acute lumbar pain in the moment of the realization.
  • Neurological or orthopedic desease.
  • Any important estructural alteration in the lower members that may be likely to alter the results under study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Fascial treatment
Treatment the lumbar fasciae
Treat the lumbar facial with a manual technique
Placebo Comparator: Placebo group
Introduce in a machine off
Introduce in a machine off

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Straight Leg Raising Test (SLR)
Time Frame: Pre-intervention and immediately after the intervention
Test
Pre-intervention and immediately after the intervention
Change from Passive Popliteal Angle Test (PKE)
Time Frame: Pre-intervention and immediately after the intervention
Test
Pre-intervention and immediately after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
IPAQ
Time Frame: Pre-intervention
Cuestionnary
Pre-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Juan Javier Bru Ruiz, Universidad Católica San Antonio de Murcia

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2019

Primary Completion (Actual)

March 1, 2019

Study Completion (Actual)

April 30, 2019

Study Registration Dates

First Submitted

April 6, 2020

First Submitted That Met QC Criteria

April 9, 2020

First Posted (Actual)

April 14, 2020

Study Record Updates

Last Update Posted (Actual)

April 14, 2020

Last Update Submitted That Met QC Criteria

April 9, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • CONSORT

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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