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Comparison of the effect of trigger point acupuncture and traditional acupuncture on low back pain.

Comparison of the effect of trigger point acupuncture and traditional acupuncture on low back pain.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201207049636N1
Enrollment
48
Registered
2021-04-23
Start date
2021-05-05
Completion date
Unknown
Last updated
2021-05-26

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

Conditions

low back pain. Low back pain

Interventions

Intervention 1: 1st Intervention group: In the trigger point acupuncture group, the treatment will be performed for up to 6 sessions, Once every two days, for 12 days with disposable dong-bang needles

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Of the patients who presented with complaints of low back pain, 48 patients were studied. Patients should be in the age range of 18 to 60 years. All patients should have at least one active trigger point. Patients must have a vas (visual analog scale) score more than 4.

Exclusion criteria

Exclusion criteria: Pregnancy Neuromuscular junction disorders Neurological defects found in electromyography Progressive neurological defects Urinary or fecal incontinence following pain Progressive decrease in muscle strength Lumbar orthopedic disorders or a history of lumbar surgery Rheumatologic disorders Diagnosed history of hip and sacroiliac joint problems Known psychological disorders Cancer

Design outcomes

Primary

MeasureTime frame
Pain reported by the patient in the vas questionnaire. Timepoint: The beginning of the intervention, one week, one month and three months later. Method of measurement: Vas pain measurement questionnaire.

Secondary

MeasureTime frame
Patient's disability based on Oswestry Disability Index (ODI) questionnaire. Timepoint: The beginning of the intervention, one week, one month and three months later. Method of measurement: ODI Disability Questionnaire.;Kinesiophobia. Timepoint: The beginning of the intervention, one week, one month and three months later. Method of measurement: kinesiophobia TSK (Tampa Scale of Kinesiophobiais) Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKorosh Mansori

Iran University of Medical Sciences

mansori.k@iums.ac.ir+98 21 8214 1600

Outcome results

None listed

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