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The effect of dry needling in subjects with fibromyalgia with low back pain

The effect of dry needling on pain intensity, pressure pain threshold, remote muscle performance and disability in subjects with fibromyalgia and chronic nonspecific low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191208045652N7
Enrollment
30
Registered
2023-03-11
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Condition 1: Fibromyalgia. Condition 2: Chronic Nonspecific Low Back Pain. Fibromyalgia Low back pain

Interventions

Intervention 1: Intervention group: Performing dry needling technique for lumbar multifidus, quadratus lumborum and gluteus medius. In order to apply dry needling to the lumbar multifidus muscle, the

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: People aged 18 to 65 Fibromyalgia diagnosed by a rheumatologist The pain should be between the edge of the 12th rib and the lower gluteal fold The duration of pain is more than three months The minimum Visual analogue scale at the time of visit should be 3 out of 10 Patients have trigger points in the multifidus, quadratus lumborum and gluteus medius muscles Have a minimum Oswestry Disability Index score of 20 out of 100 The participants should be able to understand and read Persian language in order to fill the questionnaire

Exclusion criteria

Exclusion criteria: Spinal and pelvic pathologies such as fracture, infection and tumor Presence of systemic infection Coagulation and bleeding disorders Presence of lymphedema or removal of lymph nodes pregnancy The presence of a pacemaker Severe respiratory and cardiovascular disorders epilepsy History of trauma to the lumbopelvic region History of surgery in the lumbopelvic region Lumbar radiculopathy Dry needling treatment in the last 6 months Cognitive impairment Needle phobia Uncontrolled diabetes Systemic joint disease such as rheumatoid arthritis Symptoms of radiculopathy and pressure on the nerve root Cauda equina? syndrome Spondyloarthropathies Metal pins or prosthetic joints Inability to communicate with the patient

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The first session before treatment, the fourth session before the start of the treatment, the sixth session before the start of the treatment, one month after the last treatment session, three months after the last treatment session. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Muscle performance. Timepoint: The first session before treatment, the sixth session before the start of the treatment, one month after the last treatment session. Method of measurement: dynamometer and Isometric test of neck flexor muscles.;Pressure pain threshold. Timepoint: The first session before treatment, the sixth session before the start of the treatment, one month after the last treatment session. Method of measurement: Algometer.;Functional disability. Timepoint: The first session before treatment, the sixth session before the start of the treatment, one month after the last treatment session. Method of measurement: Oswestry disability index.;Central sensitization. Timepoint: The first session before treatment, the sixth session before the start of the treatment, one month after the last treatment session. Method of measurement: fibromyalgia 2011 questionnaire, Algometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoume Matin

Iran University of Medical Sciences

mmatin.pt@gmail.com+98 21 2225 6434

Outcome results

None listed

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