- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06751160
Comparative Effects of Dry Needling Versus Soft Tissue Mobilization on Hamstring Tightness
Comparative Effects of Dry Needling Versus Soft Tissue Mobilization on Hamstring Tightness in Chronic Low Back Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad, PhD
- Phone Number: 03324390125
- Email: Imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Recruiting
- Hameed Latif Medical Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Reduction in active knee extension test >25
- Current back pain between 4 to 6 on Numeric Pain Rating scale
- Low back pain for at least 12weeks0r 6 months
Exclusion Criteria:
- Subjects using anticoagulants and having vascular diseases
- Subjects with needle phobia and allergic to metals
- Subjects with cognitive impairment
- History of fracture in lumbar region
- History of systemic diseases e.g. cancer or systemic joint pathologies
- History of congestive heart failure in past 24 months
- Subjects have used medications like narcotics or Muscle relaxants 30 days before enrolment into study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dry Needling
Dry Needling along with baseline treatment
|
Baseline Treatment: Hot pack will be applied for 15 minutes on Hamstrings and lower back and transcutaneous electrical nerve stimulation (TENS) at lower back for warm up and pain relief to both groups. Then spinal mobilization (Poster lateral glide) of grade 1 and 2 (3 sets of 6 repetitions) i.e. within the spine resistance. Dry Needling will be given to group A along with baseline treatment through following protocol: Patient will be in prone lying. Sterilized disposable dry needles of 0.25*60mm will be used. Dry needling will be performed on three points on Hamstring muscle for one minute each. We considered a line between ischial tuberosity and head of fibula to target long head of bicep femoris (60% of line) and short head of bicep femoris (30% of line). Semitendinosus and Semi Membranosus were targeted at a point of 60% of line from ischial tuberosity to medial epicondyl of femur. Sessions: Total 8 sessions will be given 2 sessions per week for 4 weeks.
Other Names:
|
|
Experimental: Soft Tissue Mobilization
Soft Tissue Mobilization along with baseline treatment
|
Baseline Treatment: Hot pack will be applied for 15 minutes on Hamstrings and lower back and transcutaneous electrical nerve stimulation (TENS) at lower back for warm up and pain relief to both groups. Then spinal mobilization (Poster lateral glide) of grade 1 and 2 (3 sets of 6 repetitions) i.e. within the spine resistance. Soft Tissue Mobilization will be given to Group B along with Baseline treatment. Subject will be in prone lying position with knee bent at 30 to 60 degrees. Soft tissue mobilization will be applied on hamstring muscle through Graston technique. Massage cream will be applied on hamstring muscle and Graston Instrument will be rubbed from gluteal line to politeal fossa 30 times for 60 seconds. Sessions: Total 8 sessions will be given 2 sessions per week for 4 weeks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: 4 weeks
|
Numeric Pain Rating Scale (NPRS) was used to measure low back pain.
NPRS consists of 11 points, which range from 0= no pain, 1-4= mild pain, 4-7= moderate pain 7-10= severe pain .
Researchers states that NPRS shows High test to re test reliability (ICC 0.96) in elderly populations with musculoskeletal disorders without having cognitive dysfunction.
|
4 weeks
|
|
Oswestry Disability index (Urdu)
Time Frame: 4 weeks
|
The Oswestry Disability index (ODI) consists of 10 patient- completed questions in which the response options are presented as 6-point Likert scales.
Scores range from 0% (no disability) to 100% (most severe disability).
|
4 weeks
|
|
Inclinometer
Time Frame: 4 weeks
|
It was used to measure range of motion of low back.
An instrument for measuring angles is an inclinometer.
A sensor is housed in the housing of an inclinometer.
The sensor measures the housing's tilt and is sensitive to gravity.
After that, the angle is shown on a dial or digital display.
|
4 weeks
|
|
Active Knee Extension Test
Time Frame: 4 Week
|
The most effective way to exclude the hamstring muscle's extensibility range, with the hip fixed at a 90-degree angle and precise instrument placement, is to perform the active knee extension test.
This technique provides accurate measures of hamstring length and extensibility when used in a supine 90/90 position.
Both a normal goniometer and an electrogoniometer were used to measure the amount of extension.
Whether hamstring tightness contributes to mechanical low back pain can be inferred from this result.
|
4 Week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ali Raza, MS-OMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/24/0106
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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