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Clinical Trials/CTRI/2025/08/092438
CTRI/2025/08/092438
Not yet recruiting
Phase 1

Effectiveness of Dry Needling for Hamstring and Quadratus Lumborum in Managing Pain and Disability in Chronic Low Back Pain: A Comparative Analysis

Tannu1 site in 1 country54 target enrollmentStarted: August 17, 2025Last updated:

Overview

Phase
Phase 1
Status
Not yet recruiting
Sponsor
Tannu
Enrollment
54
Locations
1
Primary Endpoint
Pain, Hamstring Flexibility,

Overview

Brief Summary

Low back pain is a widespread condition that affects many people at some point in their lives. Chronic Low Back Pain is a recognized public health issue that tends to worsen over time, often leading to the formation of trigger points in the quadratus lumborum (QL) muscle and hamstring tightness, which is commonly associated with chronic low back pain. The available literature stated that needling to hamstring and quadratus lumborum helps to ease the chronic low back pain but till now none of the study compare their effects like which one is better one. The present study analyses the effect of dry needling on hamstring and quadratus lumborum to assess which approach is better one to  improving pain, functionality, mobility, quality of life in patients with chronic low back pain.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant Blinded

Eligibility Criteria

Ages
25.00 Year(s) to 45.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • The study will include the patients of specific and non specific chronic back pain which persist more than 3 months.
  • The subjects will not be taken any physiotherapy treatment from last 4 months.

Exclusion Criteria

  • The subjects will be excluded who having Red flags indicative of serious spinal pathology with signs and symptoms of nerve root compromise.
  • Any obvious spinal deformity or neurological diseases.
  • A reported history of cardiovascular diseases contraindicated to exercise; or individuals who were with elevated blood pressure.
  • Chronic low back pain due to rheumatoid arthritis, ankylosing spondylitis, Lumbar scoliosis, radiculopathies, tumors, or chronic rheumatological diseases, including axial spondyloarthritis (axSpA).
  • Fibromyalgia, corticosteroids or other oral medications treatment and history of spinal surgery.
  • Contraindications for dry needle (needle phobia, coagulation or psychological disorders, varicose regions, cysts, wound, metal or latex allergy, lymphedema, hypothyroidism, diabetes.
  • Those participants with hamstring tightness and pregnancy.
  • Subjects who do not meet the age group.

Outcomes

Primary Outcomes

Pain, Hamstring Flexibility,

Time Frame: At baseline and after 6 weeks of intervention.

Lumbar Flexibility, Disability,

Time Frame: At baseline and after 6 weeks of intervention.

and Quality of life.

Time Frame: At baseline and after 6 weeks of intervention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Tannu
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Tannu

Guru Nanak Dev University

Study Sites (1)

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