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effect of lumbopelvic manipulation on neuroplasticity in non specific chronic low back pain

Evaluation of the effects of lumbopelvic manipulation on the central nervous system plasticity in non-specific chronic low back pain patients with sacroiliac joint origin by magnetic resonance spectroscopy technique.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150923024149N15
Enrollment
25
Registered
2018-01-05
Start date
2017-12-23
Completion date
Unknown
Last updated
2018-02-22

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. Dorsalgia, unspecified, Backache NOS

Interventions

Intervention 1: Test group: They are asked to not use any medication during the course of the study. In this stage of treatment, the test group receives 3 sessions of lumbar and pelvic spinal manipula
Treatment - Other
Test group: They are asked to not use any medication during the course of the study. In this stage of treatment, the test group receives 3 sessions of lumbar and pelvic spinal manipulation.
Quasi-test: They are asked to not use any medication during the course of the study. At this stage, patients undergo 3 sessions of spinal alignment, similar to the lumbopelvic spinal manipulation.

Sponsors

Shiraz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: patients with chronic non specific low back pain Age between 20 and 50 years pain NRS between 3-7 3 or more positive test of SIJ test( ditraction test, compression test, thigh trust test, geanslen test,FABER test and sacral trust test) They have not been treated for the last three months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Brain metabolite. Timepoint: pre and 5 weeks post intervention. Method of measurement: magnetic resonance spectroscopy.

Secondary

MeasureTime frame
Pain. Timepoint: pre and 5 weeks post intervention. Method of measurement: numerical rating scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Kamali

Shiraz University of Medical Sciences

kamalif@sums.ac.ir+98 71 3627 1552

Outcome results

None listed

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