NCT07258537

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2024

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 22, 2024

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

July 22, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

December 2, 2025

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 22, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 22, 2025

Completed
Last Updated

December 2, 2025

Status Verified

September 1, 2025

Enrollment Period

1.3 years

First QC Date

July 22, 2025

Last Update Submit

November 28, 2025

Conditions

Sacroiliac Joint Dysfunction

Outcome Measures

Primary Outcomes (1)

  • numeric pain rating scale

    Numeric pain rating scale: ranging from 0 ("no pain") to 10 ("worst possible pain")

    6 weeks

Study Arms (1)

1

EXPERIMENTAL

modified SIM

Other: modified SIM manipulation

Interventions

modified SIM manipulationOTHER

manipulation

1

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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.)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rasool Medical Complex

Gujrat, Punjab Province, 52000, Pakistan

Location

Study Officials

  • Prof. Dr. Ashfaq Ahmed, PHD PT

    University of Lahore

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 22, 2025

First Posted

December 2, 2025

Study Start

August 22, 2024

Primary Completion

December 22, 2025

Study Completion

December 22, 2025

Last Updated

December 2, 2025

Record last verified: 2025-09

Locations

PA(1)