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Efficacy and Functional Mechanism of a Pelvic Compression Belt for Patients with Sacroiliac Joint Pain

Efficacy and Functional Mechanism of a Pelvic Compression Belt for Patients with Sacroiliac Joint Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013127
Enrollment
40
Registered
2017-10-16
Start date
2017-10-19
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Sacroiliac Joint Pain

Interventions

Group 1: pelvic compression belt SacroLoc II for 6 weeks, 4 to 6 hours daily Group 2: no intervention that is connected to the study over a period of six weeks

Sponsors

Bauerfeind AG
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - age of majority - pain in the lumbosacral area for at least eight weeks - at least three positive SIJP provocation tests out the following: compression test, distraction test, Gaenslen test, Faber/Patrick's test, thigh thrust test, sacral thrust test, drop test

Exclusion criteria

Exclusion criteria: - musculoskeletal disease - heart and circulatory disease - pregnancy - pathological gait - contracturs - endoprosthetics - infections - somatoform disorders

Design outcomes

Primary

MeasureTime frame
Pain intensity is measured with the SF12 questionnaire once on each examination day (first examination at the start of the study, second examination after a six week intervention period) to assess the pain intensity level over the preceding weeks. Additionally, the Numeric Rating Scale (NRS) is used to assess the current pain intensity of the patient. This scale is used twice per examination – once without the pelvic belt and once with applied pelvic belt. Thus, it is possible to investigate short- and long-term effects of the pelvic compression belt on pain intensity.

Secondary

MeasureTime frame
Dynamic balance will be measured in an upright, standing position in medio-lateral, anterior-posterior direction via Posturomed. Center of Pressure (CoP) data will be collected to analyze corresponding parameters like CoP distance, CoP velocity, 95% confidence ellipse and envelope curve. CoP data will be collected twice per examination - once without the pelvic belt and once with applied pelvic belt. Thus, it will be possible to investigate short- and long-term effects of the pelvic compression belt on dynamic balance. The Y-Balance-Test makes it possible to assess coordination and mobility by measuring reach distances of the lower limbs in anterior, postero-lateral and postero-medial directions. The test will be performed twice per examination - once without the pelvic belt and once with applied pelvic belt. Thus, it is possible to investigate short- and long-term effects of the pelvic compression belt on mobility and coordination.

Countries

Germany

Contacts

Public ContactChristin Büttner

Technische Universität Chemnitz

christin.buettner@hsw.tu-chemnitz.de+4937153131813

Outcome results

None listed

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