POS Mobilization by 3-DRT Affect Functional Outcome in Layered Syndrome
16 juli 2026 uppdaterad av: 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
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Faktisk)
44
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Punjab Province
-
Sialkot, Punjab Province, Pakistan, 51310
- Imran Idrees teachingHospital
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Nej
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: POS mobilization
Posterior oblique sling mobilization by 3-D release technique along with conventional physiotherapy treatment for Upper cross and lower cross syndrome
|
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
|
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
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Neck disability Index
Tidsram: 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
Tidsram: 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
Tidsram: 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
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Numeric Pain rating sclae (NPRS)
Tidsram: 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)
Tidsram: 4rth week
|
Changes from the baseline ROM range of cervical spine flexion was taken
|
4rth week
|
|
ROM Cervical Spine (Extension)
Tidsram: 4rth
|
Changes from the baseline ROM range of cervical spine extension was taken
|
4rth
|
|
ROM Cervical Spine (Lateral Flexion)
Tidsram: 4rth
|
Changes from the baseline ROM range of cervical spine lateral flexion was taken
|
4rth
|
|
ROM Lumbar Spine (Flexion)
Tidsram: 4rth
|
Changes from the baseline ROM range of lumbar spine flexion was taken
|
4rth
|
|
ROM Lumbar Spine (Extension)
Tidsram: 4rth
|
Changes from the baseline ROM range of lumbar spine extension was taken
|
4rth
|
|
ROM Shoulder joint (Flexion)
Tidsram: 4rth
|
Changes from the baseline ROM range of shoulder joint flexion was taken
|
4rth
|
|
ROM Shoulder joint (Abduction)
Tidsram: 4rth
|
Changes from the baseline ROM range of shoulder joint abduction was taken
|
4rth
|
|
ROM Shoulder joint (External Rotation)
Tidsram: 4rth
|
Changes from the baseline ROM range of shoulder joint external rotation was taken
|
4rth
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Saba Rafique, Phd*, Riphah International University
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
1 december 2025
Primärt slutförande (Faktisk)
1 maj 2026
Avslutad studie (Faktisk)
1 maj 2026
Studieregistreringsdatum
Först inskickad
17 juni 2026
Först inskickad som uppfyllde QC-kriterierna
16 juli 2026
Första postat (Faktisk)
17 juli 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
17 juli 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
16 juli 2026
Senast verifierad
1 juli 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- REC/RCR&AHS/25/0127
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .