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Clinical Trials/NCT04668092
NCT04668092
Completed
Not Applicable

Immediate Effects of Functional Dry Needling on the Length of Shortened Hamstring Muscle

Riphah International University1 site in 1 country27 target enrollmentFebruary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hamstring Contractures
Sponsor
Riphah International University
Enrollment
27
Locations
1
Primary Endpoint
90-90 Straight Leg Raise (SLR)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The aim of this study is to find whether functional dry needle is helpful to increase the length of shortened hamstring muscle or not

Detailed Description

Single pretest-post clinical trial to find immediate effects of functional dry needling to increase the length of the shortened hamstring. This study will be carried on single group which will include male subjects only. The data will be recorded before and immediately after the treatment. A monofilament stainless steel needle will be inserted on three points on hamstring muscle which will include semitendinosus, semimembranosus and bicep femoris. Treatment session will consist of 1 minute 20 seconds for each point on the hamstring and the manipulation will be performed by "Pistoning technique" in which the needle will be drawn out (not fully out of skin) after inserted and then again pushed in and data will be recorded after the treatment session on the basis of increase in length of hamstring which will be measure through 90-90 SLR (AKE) and on the lower extremity functional scale (LEFS)

Registry
clinicaltrials.gov
Start Date
February 1, 2019
End Date
December 6, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Having hamstring length less than 80 degree during 90-90 SLR on goniometer,
  • also the subject that suffers from knee Osteoarthritis,
  • Spondylosis,
  • Lumber radiculopathy,
  • Subjects with MTrPs and those with hyper lordosis were recruited in the study

Exclusion Criteria

  • subjects suffering from blood clotting disorders such as hemophilia,
  • those with deformities such as leg length discrepancy,
  • compromised immune system,
  • vascular diseases,
  • Diabetes,
  • People with congenital or metabolic bone disease such as Spondyloepiphyseal Dysplasia and Pregnancy were excluded from the study

Outcomes

Primary Outcomes

90-90 Straight Leg Raise (SLR)

Time Frame: 1 day

90-90 Straight Leg Raise (SLR) test is used to measure hamstring length through goniometer. The patient lie supine and flex the hip and extend the knee. The test is positive if the patient cannot go withing last 20 degrees of knee extension.

Secondary Outcomes

  • Lower extremity Functional scale (LEFS)(1 day)

Study Sites (1)

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