NCT07052552

Brief Summary

With the advent of the Internet, mobile phones and other electronic devices have become an integral component in everyone's lives, especially students, whether it is to attend classes, make purchases, conduct transactions, or have social interactions . The continuous use of these electronic devices can easily result in abnormal postures . Upper crossed syndrome (UCS) is one of the most frequently cited complications with modern technological life, which is characterized by weakened middle and lower trapezius, scalenes, deep cervical flexors and serratus anterior at the same time as the rhomboids, as well as tightness in the upper trapezius, pectoralis minor and major and levator scapulae muscles . It mainly leads to muscle imbalances, which eventually manifest in both tonic and phasic muscles

Trial Health

87
On Track

Trial Health Score

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

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 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

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 4, 2025

Completed
28 days until next milestone

Study Start

First participant enrolled

August 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

November 19, 2025

Status Verified

November 1, 2025

Enrollment Period

2 months

First QC Date

June 26, 2025

Last Update Submit

November 15, 2025

Conditions

Keywords

Ujjayi pranayamaOsteopathic ManipulationUpper cross syndrome

Outcome Measures

Primary Outcomes (7)

  • FVC ( liters )

    Forced vital capacity (FVC) is the total amount of air exhaled during the FEV test. Forced expiratory volume and forced vital capacity are lung function tests , using portable spirometer ( SP 80B , China )

    Pre and post 8 weeks

  • FEV1 ( liters )

    Forced expiratory volume in 1 second that can reflect pulmonary function , using portable spirometer ( SP 80B,China)

    Pre and post 8 weeks

  • FEV1/FVC ( % )

    The ratio of the forced expiratory volume in the first one second to the forced vital capacity of the lungs. That can reflect pulmonary function , using portable spirometer ( SP 80B,China)

    pre and post 8 weeks

  • PEF ( liters / minute )

    Peak expiratory flow (PEF), a key indicator of lung function,using portable spirometer ( SP 80B,China)

    pre and post 8 weeks

  • Expiratory reserve volume ( ERV ) ( Liters )

    is the maximum amount of air that can be forcefully exhaled after a normal, tidal exhalation

    pre and post 8 weeks

  • maximum voluntary ventilation (MVV) ( liters/minute )

    is a pulmonary function test that measures the maximum amount of air a person can breathe in and out of their lungs in one minute

    Pre and post 8 weeks

  • The inspiratory reserve volume (IRV) ( Liters )

    It represents the maximum amount of air that can be inhaled after a normal inhalation

    Pre and post 8 weeks

Secondary Outcomes (3)

  • 6MWDT ( meters )

    Pre and post 8 weeks

  • Timed up and go test ( seconds )

    Pre and post 8 weeks

  • Berg Balance Scale (BBS) to test dynamic balance

    Pre and post 8 weeks

Study Arms (2)

Control group

SHAM COMPARATOR

control group will perform osteopathic manipulative tratment only

Other: osteopathic manipulative tratment only

Experimental group

EXPERIMENTAL

experimental group will perform ujjayi pranayama and osteopathic manipulative treatment

Other: ujjayi pranayama and osteopathic manipulative treatment

Interventions

focuses on restoring proper muscle balance and joint mechanics through techniques that address the shortened, tight muscles and the lengthened, weak muscles characteristic of the syndrome

Control group

Ujjayi pranayama, often called "ocean breath," can be a helpful practice for individuals with Upper Cross Syndrome (UCS) by promoting relaxation and improving breath control. While not a direct cure, it can alleviate some symptoms and improve overall posture and body awareness. Osteopathic manipulative treatment focuses on restoring proper muscle balance and joint mechanics through techniques that address the shortened, tight muscles and the lengthened, weak muscles characteristic of the syndrome

Experimental group

Eligibility Criteria

Age20 Years - 29 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Full time college students of age 20-29 years.
  • Subjects who have upper cross syndrome according to REEDCO posture assessment.
  • Subjects who not receiving medical treatment for respiratory diseases .
  • Subjects who have clean family medical history

You may not qualify if:

  • Subjects who engaged in additional exercise in two weeks, which was likely to affect the results of the research .
  • Individuals with a history of spine, shoulder fractures, surgery, or other disease.
  • Individuals with severe cardia-cerebrovascular disease.
  • Individuals who will have difficulty to follow-up testing).
  • Neurologic and psychiatric disorders (who can not understand the research project ).
  • Individuals with congenital deformities

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mohamed Saied Zidan

Cairo, 11571, Egypt

Location

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Interventions

Manipulation, Osteopathic

Intervention Hierarchy (Ancestors)

Musculoskeletal ManipulationsComplementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor doctor

Study Record Dates

First Submitted

June 26, 2025

First Posted

July 4, 2025

Study Start

August 1, 2025

Primary Completion

September 30, 2025

Study Completion

October 1, 2025

Last Updated

November 19, 2025

Record last verified: 2025-11

Locations