Modified Sims Versus Lumbar Roll Manipulation in Patients With Sacroiliac Joint Dysfunction
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: modified SIM manipulation.
- Who it may be relevant to
- Registry conditions: Sacroiliac Joint Dysfunction. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Pakistan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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
- Other modified SIM manipulation
manipulation
Primary outcome measures
- numeric pain rating scale [Time frame: 6 weeks]
Eligibility criteria
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.)
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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Pakistan · 1 center
- Rasool Medical Complex — Gujrat
Identifiers
NCT: NCT07258537 · DPTH02193002