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immediate effect of dry needling on hamstring muscle flexibility

Study of the immediate and after one week effect of dry needling on chronic non-specific low back pain women with hamstring shortness: A placebo controlled RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180511039612N1
Enrollment
10
Registered
2018-07-02
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-specific chronic low back pain.

Interventions

Intervention 1: Intervention group:hamstring muscle is needling cone shape fast in-fast out during a therapeutic session at 3 points of muscle end plate for 1 minute at each point bilaterally. Interve

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients with chronic non-specific low back pain , without history of fracture in low back and thigh region Less than 80? of the passive knee extension (PKE) test Female gender Intensity of low back pain based on VAS , is being between 3-7 Do not be afraid of needle Do not use blood thinner such as Warfain No vascular disease No history of muscular disease such as Myopathy No Radicular pain in lower extermity Not pregnancy The duration of the low back pain should be more than 3 month No needle sensitivity Lack of epilepsy Lack of diabetes

Exclusion criteria

Exclusion criteria: Intolerance to the evaluation and treatment steps Acute low back pain and fracture in the low back and hip area between therapeutic sessions Unwillingness to continue cooperation

Design outcomes

Primary

MeasureTime frame
Intensity of low back pain. Timepoint: Before , after and one week after intervention. Method of measurement: Visual analog scale.;Hamstring muscle length. Timepoint: Before , after and one week after intervention. Method of measurement: Passive knee extension and finger to floor test.

Secondary

MeasureTime frame
Functional disability. Timepoint: Before and one week after intervention. Method of measurement: Functional rating index.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmahnaz bazzaz yamchi

Tehran University of Medical Sciences

m-bazzaz@razi.tums.ac.ir+98 21 7753 5132

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 14, 2026