NCT07710079

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

December 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 17, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 17, 2026

Completed
Last Updated

July 17, 2026

Status Verified

July 1, 2026

Enrollment Period

5 months

First QC Date

June 17, 2026

Last Update Submit

July 16, 2026

Conditions

Keywords

DisabilityPainRange of motion

Outcome Measures

Primary Outcomes (3)

  • Neck disability Index

    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

    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

    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

Secondary Outcomes (9)

  • Numeric Pain rating sclae (NPRS)

    4rth week

  • ROM Cervical Spine (Flexion)

    4rth week

  • ROM Cervical Spine (Extension)

    4rth

  • ROM Cervical Spine (Lateral Flexion)

    4rth

  • ROM Lumbar Spine (Flexion)

    4rth

  • +4 more secondary outcomes

Study Arms (2)

POS mobilization

EXPERIMENTAL

Posterior oblique sling mobilization by 3-D release technique along with conventional physiotherapy treatment for Upper cross and lower cross syndrome

Other: POS Mobilization

Coventional Physical therapy

ACTIVE COMPARATOR

Cervical isometrics and stretching, Lumbar isometrics and stretching

Other: Conventional Physical Therapy

Interventions

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

Coventional Physical therapy

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

POS mobilization

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Imran Idrees teachingHospital

Sialkot, Punjab Province, 51310, Pakistan

Location

Related Publications (1)

  • Welling A, Patil A, Gunjal P, Naik P, Hubli R. Effectiveness of Three-Dimensional Myofascial Release on Lumbar Lordosis in Individuals with Asymptomatic Hyperlordosis: A Placebo Randomized Controlled Trial. Int J Ther Massage Bodywork. 2024 Jun 13;17(2):20-31. doi: 10.3822/ijtmb.v17i2.957. eCollection 2024 Jun.

    PMID: 38873188BACKGROUND

MeSH Terms

Conditions

Shoulder PainNeck PainLow Back PainPain

Condition Hierarchy (Ancestors)

ArthralgiaJoint DiseasesMusculoskeletal DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBack Pain

Study Officials

  • Saba Rafique, Phd*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

June 17, 2026

First Posted

July 17, 2026

Study Start

December 1, 2025

Primary Completion

May 1, 2026

Study Completion

May 1, 2026

Last Updated

July 17, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations