NCT07642713

Brief Summary

The study aims to determine whether lumbopelvic manipulation yields superior improvements in pain, pelvic alignment, and functional ability when combined with METs compared to the treatment provided through METs solely.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 8, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 11, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

June 15, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 10, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 10, 2026

Last Updated

June 11, 2026

Status Verified

June 1, 2026

Enrollment Period

4 months

First QC Date

June 8, 2026

Last Update Submit

June 8, 2026

Conditions

Keywords

ManipulationDisabilityGirdle painMuscle Stretching

Outcome Measures

Primary Outcomes (3)

  • Numeric Pain Rating Scale (NPRS) for pain

    This instrument is commonly used to rate the severity of pain. A scale of 0 to 10 is used by patients to rate their present level of pain, with 0 indicate "no pain" and 10 indicate the "worst possible pain. The patient verbally report number between 0 to 10. NPRS demonstrate strong measurement properties in patients with low back pain

    4 weeks

  • Oswestry Disability Index (ODI) for functional disability

    ODI version 2 was used in this study assess functional disability associated with low back pain and sacroilliac joint dysfunction. ODI is standardized and widely used self-reported questionnaire evaluate impact of pain on activities of daily living and functional status. It consists of 10 sections including pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sex life, social life, and traveling. Each domain consists of six items that are ranked from 0 to 5, with 0 being no disability and 5 being maximum disability.

    4 weeks

  • Clinometer:

    Smart Phone based inclinometer is a digital tool to measure body segmental angel when placed on Anatomical landmark Such as ASIS and PSIS and estimate pelvic tilt angel in standing and sitting position and align them using tape. This smart phone-based measurement tool has Reliability intra-rater: ICC = 0.87 and inter-rater: ICC = 0.82 in standing and in sitting intra-rater: ICC = 0.91 and inter-rater: ICC = 0.88 show excellent reproducibility and consistency of measurement.

    4 weeks

Study Arms (2)

lumbopelvic manipulation and METs

EXPERIMENTAL

Group A will receive baseline treatment with lumbopelvic manipulation and METs

Other: Lumbopelvic manipulation and METs

METs

ACTIVE COMPARATOR

Group B will receive baseline treatment with METs

Other: METs

Interventions

METsOTHER

Group A will undergo METs

METs

Group A will undergo Lumbopelvic manipulation and METs

lumbopelvic manipulation and METs

Eligibility Criteria

Age25 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsAnterior tilt more common in females
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Participants' age range 25\_40 years.
  • Females
  • Have subacute (4-12 weeks) pain close to PSIS
  • Have ≥3/4 positive test PSIS height, standing flexion, prone knee flexion, supine to long sitting
  • Two out of four positive tests of pain provocation Distraction, compression, thigh thrust, and sacral thrust test)
  • Patients have moderate pain on the NPRS

You may not qualify if:

  • Participants with True leg length Differences
  • Systemic illnesses, such as ankylosing spondylitis or RA, or pregnancy
  • Individuals with anticoagulation or bleeding disorders, acute muscle trauma, infections, lumbar disc herniation, spinal deformities, or a history of spinal surgery or anticoagulation medication
  • No history of fracture

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rehab Cure

Lahore, Punjab Province, 54000, Pakistan

Location

Related Publications (4)

  • Bibrowicz K, Ogrodzka-Ciechanowicz K, Hudakova Z, Szurmik T, Bibrowicz B, Kurzeja P. Pelvic Asymmetry and Stiffness of the Muscles Stabilizing the Lumbo-Pelvic-Hip Complex (LPHC) in Tensiomyography Examination. J Clin Med. 2025 Mar 25;14(7):2229. doi: 10.3390/jcm14072229.

    PMID: 40217684BACKGROUND
  • Chu ECP, Wong AYL. Change in Pelvic Incidence Associated With Sacroiliac Joint Dysfunction: A Case Report. J Med Cases. 2022 Jan;13(1):31-35. doi: 10.14740/jmc3816. Epub 2022 Jan 17.

    PMID: 35211233BACKGROUND
  • Fiani B, Sekhon M, Doan T, Bowers B, Covarrubias C, Barthelmass M, De Stefano F, Kondilis A. Sacroiliac Joint and Pelvic Dysfunction Due to Symphysiolysis in Postpartum Women. Cureus. 2021 Oct 9;13(10):e18619. doi: 10.7759/cureus.18619. eCollection 2021 Oct.

    PMID: 34786225BACKGROUND
  • Akram H, Bashir MS, Zia A, Noor R, Shakeel A. Comparison of muscle energy technique and mobilization with movement to reduce pain and improve functional status in subjects with anterior innominate ilio-sacral dysfunction. J Bodyw Mov Ther. 2024 Oct;40:1336-1341. doi: 10.1016/j.jbmt.2022.11.003. Epub 2022 Dec 5.

    PMID: 39593454BACKGROUND

MeSH Terms

Interventions

ETV3 protein, human

Study Officials

  • Hira Shaukat, Mphill

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 8, 2026

First Posted

June 11, 2026

Study Start

June 15, 2026

Primary Completion (Estimated)

October 10, 2026

Study Completion (Estimated)

November 10, 2026

Last Updated

June 11, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations