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Functional DN for Shortened HS Muscle

Primary Purpose

Hamstring Contractures

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Functional dry needling
Sponsored by
Riphah International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hamstring Contractures focused on measuring Dry needling, LEFS, 90-90 SLR

Eligibility Criteria

18 Years - 40 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Having hamstring length less than 80 degree during 90-90 SLR on goniometer,
  • also the subject that suffers from knee Osteoarthritis,
  • Spondylosis,
  • LBP,
  • 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

Sites / Locations

  • Saidu group of teaching hospital said sharif swat

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Functional dry needling

Arm Description

Functional dry needling for shortened hamstring muscle

Outcomes

Primary Outcome Measures

90-90 Straight Leg Raise (SLR)
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 Outcome Measures

Lower extremity Functional scale (LEFS)
Lower extremity Functional Scale is a 20 content scale design to measure the disability level of the patient on the basis of function of the lower extremity. Score ranges from "0" to "80". The lower the score the greater is the disability.

Full Information

First Posted
December 9, 2020
Last Updated
March 8, 2022
Sponsor
Riphah International University
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1. Study Identification

Unique Protocol Identification Number
NCT04668092
Brief Title
Functional DN for Shortened HS Muscle
Official Title
Immediate Effects of Functional Dry Needling on the Length of Shortened Hamstring Muscle
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
November 20, 2020 (Actual)
Study Completion Date
December 6, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Riphah International University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hamstring Contractures
Keywords
Dry needling, LEFS, 90-90 SLR

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
assessor who helped to record the measurement was blinded
Allocation
N/A
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Functional dry needling
Arm Type
Experimental
Arm Description
Functional dry needling for shortened hamstring muscle
Intervention Type
Other
Intervention Name(s)
Functional dry needling
Intervention Description
functional dry needling applied to hamstring for 1 minute and post interventional data collected
Primary Outcome Measure Information:
Title
90-90 Straight Leg Raise (SLR)
Description
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.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Lower extremity Functional scale (LEFS)
Description
Lower extremity Functional Scale is a 20 content scale design to measure the disability level of the patient on the basis of function of the lower extremity. Score ranges from "0" to "80". The lower the score the greater is the disability.
Time Frame
1 day

10. Eligibility

Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
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, LBP, 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Muhammad Affan Iqbal, Phd*
Organizational Affiliation
Riphah International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saidu group of teaching hospital said sharif swat
City
Swat
State/Province
Kpk
ZIP/Postal Code
19130
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
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Functional DN for Shortened HS Muscle

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