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Modified Sims Versus Lumbar Roll Manipulation in Patients With Sacroiliac Joint Dysfunction

Modified Sims Versus Lumbar Roll Manipulation in Patients With Sacroiliac Joint Dysfunction

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07258537
Enrollment
60
Registered
2025-12-02
Start date
2024-08-22
Completion date
2025-12-22
Last updated
2025-12-02

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

Conditions

Sacroiliac Joint Dysfunction

Brief summary

This randomized controlled trial aims to compare the efficacy of two manual therapy techniques. Modified Sims Manipulation and Lumbar Roll Manipulation in treating Sacroiliac Joint Dysfunction (SIJD). The study will examine their effects on pain, quality of life, and well-being.

Detailed description

The study investigates the short- and long-term therapeutic benefits of two different high-velocity low-amplitude thrust techniques, specifically Modified Sims and Lumbar Roll Manipulation, administered along with conventional therapy. Outcomes will be measured using NPRS, SF-36, WHO-5, and gait analysis (MaxTRAQ). Patients will be randomly assigned and blinded to the treatment group. Data collection will be conducted at Rasool Medical Complex, Gujrat.

Interventions

OTHERmodified SIM manipulation

manipulation

Sponsors

University of Lahore
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Age 19-50 Either gender Chronic LBP \>1 month 3 or more positive SIJ provocation/motion tests NPRS ≥3 at baseline

Exclusion criteria

Pelvic fracture MRI-confirmed nerve root compression Psoriatic/Reactive Arthritis Elevated ESR/CRP Neurological signs Severe pain (NPRS \>8) Other red flags (malignancy, fever, etc.) \-

Design outcomes

Primary

MeasureTime frameDescription
numeric pain rating scale6 weeksNumeric pain rating scale: ranging from 0 (no pain) to 10 (worst possible pain)

Countries

Pakistan

Outcome results

None listed

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