Effect of dry needling technique of iliopsoas muscle

The effect of iliopsoas muscle dry needling technique on the clinical symptoms of subject with non-specific low back Pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200215046499N4

Enrollment

Registered

2023-09-24

Start date

2024-10-22

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

Non-specific low back Pain. low back pain

Interventions

Intervention 1: Intervention group: In addition to receiving dry needling during 6 sessions (with a sterile dong bang needle with a size of 30*50 mm), they are included in the conventional physiothera

Eligibility

Sex/Gender

All

Age

30 Years to 65 Years

Inclusion criteria

Inclusion criteria: People between 30 and 65 years old Chronic back pain that lasts for 3 months or more People with a disability score of >40 in the QBPDS Questionnaire) Not receiving any other physiotherapy treatment while participating in the study The presence of a trigger point in the muscle Iliposoas

Exclusion criteria

Exclusion criteria: Patients with sensory and/or coagulation disorders History of spine surgery Heart complications Simultaneous severe disease of the central or peripheral nervous system, Epilepsy Needle phobia Serious pathologies Specific back pain (for example, the presence of spinal canal stenosis, spondylolisthesis, tumors, etc.) People who have contraindications for transcutaneous electrical stimulation (TENS) and (US) will be excluded

Design outcomes

Primary

Measure	Time frame
Pain intensity of trigger points. Timepoint: Before and after intervention. Method of measurement: Algometer.	—

Secondary

Measure	Time frame
Pain intensity of back. Timepoint: Before and after intervention. Method of measurement: Numeric pain rating scale (NPRS).;Intensity of depression and anxiety. Timepoint: Before and after intervention. Method of measurement: Hospital Anxiety and Depression Scale( HADS).;Intensity of functional disability. Timepoint: Before and after intervention. Method of measurement: Quebec back pain disability scale(QBPDS).;Pain pressure threshold of trigger points. Timepoint: Before and after intervention. Method of measurement: Algometer.	—

Measure

Time frame

Pain intensity of back. Timepoint: Before and after intervention. Method of measurement: Numeric pain rating scale (NPRS).;Intensity of depression and anxiety. Timepoint: Before and after intervention. Method of measurement: Hospital Anxiety and Depression Scale( HADS).;Intensity of functional disability. Timepoint: Before and after intervention. Method of measurement: Quebec back pain disability scale(QBPDS).;Pain pressure threshold of trigger points. Timepoint: Before and after intervention. Method of measurement: Algometer.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHakimeh adigozali

Tabriz University of Medical Sciences

Adigozalih@tbzmed.ac.ir+98 41 3337 5359

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026