Functional DN for Shortened HS Muscle

NCT ID: NCT04668092

Last Updated: 2022-03-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-02-01
• Study Completion Date: 2020-12-06

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)

Conditions

Hamstring Contractures

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Functional dry needling

Functional dry needling for shortened hamstring muscle

Group Type: EXPERIMENTAL

Functional dry needling

Intervention Type: OTHER

functional dry needling applied to hamstring for 1 minute and post interventional data collected

Interventions

Functional dry needling

functional dry needling applied to hamstring for 1 minute and post interventional data collected

Intervention Type: OTHER

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Riphah International University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Muhammad Affan Iqbal, Phd*

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

Saidu group of teaching hospital said sharif swat

Swat, Kpk, Pakistan

Countries

Pakistan

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Other Identifiers

REC/00767 Qaisar Ali Khan

Identifier Type: -

Identifier Source: org_study_id