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POS Mobilization by 3-DRT Affect Functional Outcome in Layered Syndrome

16. juli 2026 opdateret af: Riphah International University

Effects of Posterior Oblique Sling Mobilization by 3-D Release Technique on Pain, Range of Motion and Functional Disability in Layered Syndrome

I aim to study the effects of posterior oblique sling mobilization by 3-D release technique on pain, range of motion and functional disability in layered syndrome

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

In previous literature a placebo randomized control trial was conducted. To examine how 3D MFR affects lumbar range of motion and a lumbar lordosis angle in people with asymptomatic hyperlordosis. 30 participants with hyperlordosis who met the inclusion criteria were selected. Using a lottery approach, these individuals were randomly assigned to either the experiemental group or control group, keeping a 1:1 ratio. The experimental group received 3D MFR and the control group received sham 3D MFR for six sessions (3 alternate days for 2 weeks). Lumbar range of motion was assessed using modified-modified Schober's test and the lumbar lordosis angle was measured using x-ray and flexicurve.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

44

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Pakistan
    • Punjab Province
      • Sialkot, Punjab Province, Pakistan, 51310
        • Imran Idrees teachingHospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • + Craniocervical flexion test
  • + Fleshe test (Occiput to wall distance)
  • + Thomas test
  • + Straight leg raise (SLR)
  • +Push Up test
  • +Trunk Curl Up test

Exclusion Criteria:

  • Other conditions involving the shoulder (eg. rheumatoid arthritis, osteoarthritis, damage of the glenohumeral cartilage, Hill-Sachs lesion, osteoporosis, or malignancies in the shoulder region).
  • Presence of medical conditions such as cardiac disease, infections, coagulation disorder.
  • The participants with any musculoskeletal injuries in the past 6 months
  • Cervical dysfunctions affecting upper limbs
  • Lumbar Dysfunctions
  • Any fracture or other injury
  • Any systemic illness
  • Any neurological disease

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: POS mobilization
Posterior oblique sling mobilization by 3-D release technique along with conventional physiotherapy treatment for Upper cross and lower cross syndrome
Andet: POS Mobilization

In experimental group, POS mobilization was done along with cervical and lumbar isometrics and stretching.

POS mobilization by 3-D release technique along with Cervical isometrics and lumbar isometrics 10 repitionsx 1 set, 3 days/week and targeted sustained muscle stretching (pectoralis, upper trapezius, levator scapulae, iliopsoas, rectus femoris and lumbar erector spinae) for 20-30 seconds 10 repititions x 1 set 3 days/week 12 sessions were given in total
Aktiv komparator: Coventional Physical therapy
Cervical isometrics and stretching, Lumbar isometrics and stretching
Andet: Conventional Physical Therapy
Cervical isometrics and lumbar isometrics 10 repitionsx 1 set, 3 days/week and targeted sustained muscle stretching (pectoralis, upper trapezius, levator scapulae, iliopsoas, rectus femoris and lumbar erector spinae) for 20-30 seconds 10 repititions x 1 set 3 days/week 12 sessions were given in total

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Neck disability Index
Tidsramme: 4rth week
Changes from the baseline NDI is a 10-item questionnaire created by Vernon and Mior in 1991 to assess how neck pain affects daily activities such as lifting, reading, driving, personal care, sleeping, recreation, and concentration. On a scale of 0 to 5, each item has a score; higher scores correspond to more disability.
4rth week
Oswestry Disability Index
Tidsramme: 4rth week
Changes from the baseline Oswestry Disability Index (ODI) is regarded as the gold standard for assessing adults with low back pain (LBP) in terms of both disability and quality of life (QOL). The questionnaire is designed to be a self-reported survey, where patients suffering from LBP come across limitations in Activities of Daily Living (ADL's) in several health constructs like personal care, lifting, walking, sitting, standing, sleeping, sexual life, social life, and traveling. The patients indicated the effect of pain on activities. The questions having a score range from 0 to 5, giving a maximum total score of 50. Oswestry Disability Index (ODI).
4rth week
Shoulder Pain and Disability Index
Tidsramme: 4rth week
Changes from the baseline SPADI is a self-administered questionnaire designed to evaluate pain and functional impairment related to shoulder disorders. It consists of 13 items, divided into pain and disability subscales, and is often used in both clinical practice and research.
4rth week

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Numeric Pain rating sclae (NPRS)
Tidsramme: 4rth week
Changes from the baseline NPRS consists of an 11-point scale ranging from 0 to 10, where 0 represents "no pain" and 10 indicates the "worst imaginable pain."
4rth week
ROM Cervical Spine (Flexion)
Tidsramme: 4rth week
Changes from the baseline ROM range of cervical spine flexion was taken
4rth week
ROM Cervical Spine (Extension)
Tidsramme: 4rth
Changes from the baseline ROM range of cervical spine extension was taken
4rth
ROM Cervical Spine (Lateral Flexion)
Tidsramme: 4rth
Changes from the baseline ROM range of cervical spine lateral flexion was taken
4rth
ROM Lumbar Spine (Flexion)
Tidsramme: 4rth
Changes from the baseline ROM range of lumbar spine flexion was taken
4rth
ROM Lumbar Spine (Extension)
Tidsramme: 4rth
Changes from the baseline ROM range of lumbar spine extension was taken
4rth
ROM Shoulder joint (Flexion)
Tidsramme: 4rth
Changes from the baseline ROM range of shoulder joint flexion was taken
4rth
ROM Shoulder joint (Abduction)
Tidsramme: 4rth
Changes from the baseline ROM range of shoulder joint abduction was taken
4rth
ROM Shoulder joint (External Rotation)
Tidsramme: 4rth
Changes from the baseline ROM range of shoulder joint external rotation was taken
4rth

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Riphah International University

Efterforskere

  • Ledende efterforsker: Saba Rafique, Phd*, Riphah International University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. december 2025

Primær færdiggørelse (Faktiske)

1. maj 2026

Studieafslutning (Faktiske)

1. maj 2026

Datoer for studieregistrering

Først indsendt

17. juni 2026

Først indsendt, der opfyldte QC-kriterier

16. juli 2026

Først opslået (Faktiske)

17. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

17. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • REC/RCR&AHS/25/0127

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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Kliniske forsøg med Lændesmerter

Kliniske forsøg med POS Mobilization

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