Effect of Opposite Leg Position on Hamstring Flexibility in Patients With Mechanical Low Back Pain

July 26, 2021 updated by: Nasr Awad Abdelkader Othman, Cairo University

PURPOSE: this study aimed to investigate the effect of opposite knee position on hamstring flexibility BACKGROUND Hamstrings tightness is one of the most common findings in patients with LBP. It is thought that, due to the attachments of hamstrings to the ischial tuberosity, hamstrings tightness generates posterior pelvic tilt and decreases lumbar lordosis, which can result in LBP.

HYPOTHESES There will be significant difference in the hamstring flexibility with changing position of opposite knee (flexed or extended) in patients with mechanical low back pain.

RESEARCH QUESTION: Will changing position of opposite knee (flexed or extended) affect the hamstring flexibility in patients with mechanical low back pain?

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

  • The subject will be instructed to maintain 90° hip flexion in the supine position.
  • Then asked to actively extend the knee joint.
  • The degree of achieving active knee extension will be measured using a universal goniometer.
  • The average of three active knee extension measurements will be recorded used as the hamstring muscle length for the data analysis (Dong-Kyu Lee, et al., 2018).
  • This test will be done for the same limb with opposite leg extended and with opposite flexed.

Study Type

Observational

Enrollment (Actual)

73

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

      • Giza, Egypt
        • Cairo university

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 40 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

  • Male and female
  • Age range from 18-40 years old
  • With previous mentioned inclusion criteria

Description

Inclusion Criteria:

  • Patients with history of back pain and assessed with Mechanical inflammatory low back pain index and have very high grade for mechanical component.
  • Age ranges from 18-40 years.
  • The body mass index of the subject is ≤25 kg/meter square.

Exclusion Criteria:

  1. Previous trauma, fractures or surgery of the back.
  2. Malignancy of the back.
  3. Rheumatoid arthritis
  4. Spondylolysis or spondylolithesis
  5. History of lower extremity injury within 6 months prior to the 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee extension ROM
Time Frame: 30 minutes
measuring knee extension ROM from 90 degrees hip flexion with opposite-leg flexed and extended
30 minutes

Collaborators and Investigators

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

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)

April 1, 2019

Primary Completion (ACTUAL)

June 27, 2019

Study Completion (ACTUAL)

July 25, 2019

Study Registration Dates

First Submitted

September 5, 2019

First Submitted That Met QC Criteria

September 5, 2019

First Posted (ACTUAL)

September 9, 2019

Study Record Updates

Last Update Posted (ACTUAL)

July 29, 2021

Last Update Submitted That Met QC Criteria

July 26, 2021

Last Verified

March 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P.T.REC/012/002301

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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