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The Influence of the Manipulation of the Sacroiliac Joint on Low Back Pain

The Influence of the Manipulation of the Sacroiliac Joint on Low Back Pain With or Without Radiation to Lower Limbs

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03794830
Enrollment
151
Registered
2019-01-07
Start date
2018-12-04
Completion date
2019-01-04
Last updated
2019-02-08

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

Conditions

Low Back Pain, Sacroiliac Disorder

Keywords

sacroiliac joint, low back pain, Osteopathic manipulation

Brief summary

The primary focus of this study is to know the influence of sacroiliac joint manipulation on low back pain with or without radiation to lower limbs, in the lumbopelvic-hip joint

Detailed description

One of the main problems faced by physiotherapists in primary care is low back pain with or without radiation to lower limbs. Nowadays, there are a lot of types of low back pain interventions, yet despite the vast amount of research findings, the evidence remains contradictory and inconclusive: Pharmacological treatments like NSAIDs have shown result in acute low back pain but not in chronic pain; conservative interventions (ultrasound, interferential currents, mechanical traction and massage) have been studied and found ineffective. A total of 151 low back pain patients with or without radiation to lower limbs between 18-70 years old derived from the Physiotherapy Unit of Gévora Health Center (Badajoz, Spain) voluntarily entered the study

Interventions

OTHERmanipulation group (MG)

Patients were treated with sacroiliac joint osteopathic semidirect manipulation twice a week every 3 to 4 days over a period of time of 3 weeks

OTHERelectrotheraphy group (EG)

Patients were treated with micro-waves (circular antenna in lumbar area, pulsating-mode 120W for 12 minutes) and later conventional analgesic TENS (80Hz frequency, 30 minutes) 5 days per week over a period of time of 3 weeks (15 sessions)

Sponsors

University of Extremadura
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* dysfunction or sacroiliac joint hypomobility (SI) * having stopped taking anti-inflammatory medicines or analgesics three days before the study began

Exclusion criteria

* destructive injuries of the spine and pelvis * fractures * lumbar surgery * sacroiliac instability * spondylolisthesis * pregnancy in progress * cauda equina syndrome * abdominal aneurysm * infection * inflammatory arthritis * tumors * osteoporosis

Design outcomes

Primary

MeasureTime frameDescription
visual analogue scale (VAS)1 weekPain assessment from 0 to 10. 0: no pain 10: maximum pain
Oswestry disability index (ODI)1 weekdisability assessment 0% -20% (Minimum Disability) 21% -40% (Moderate disability) 41% -60% (Severe disability) 61% -100% (Disabled):
Roland Morris questionnaire1 weekdisability assessment The extreme values oscillate between 0 (absence of disability due to low back pain) and 24 (maximum possible disability)
digital algometer (Wagner, FPIX model)1 weekPain threshold assessment by pressing the sensitive points of the muscle

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026