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Clinical Trials in Egypt / NCT07786415
Recruiting Not applicable

Beyond Osteopathic Therapy: Functional Performance Following the Addition of Ujjayi Pranayama in College Students With Upper Cross Syndrome

NCT07786415 · tracked via the Priya Life Science Egypt tracker
Sponsor
Al-Zaytoonah University of Jordan
Phase
Not applicable
Started
2026-08-25
Last updated
2026-10-16

Condition(s) studied

Upper Cross SyndromeSpinal AlignmentFunctional Performance

Investigational drug(s) / intervention(s)

The experimental group will perform ujjayi pranayama and osteopathic manipulative tratmentcontrol group will perform osteopathic manipulative treatment only

The experimental group will perform ujjayi pranayama and osteopathic manipulative tratment: The experimental group will perform ujjayi pranayama and osteopathic manipulative treatment for 45 min sessions, 5 times a week for 8 weeks

control group will perform osteopathic manipulative treatment only: control group will perform osteopathic manipulative treatment only for 45 min sessions, 5 times a week for 8 weeks

Study summary

This study aims to explore the relationship between spinal alignment and functional performance in individuals with upper cross syndrome following a combined breathing and manual therapy program. It is designed as a secondary analysis of data obtained from a previously conducted randomized controlled trial, with the addition of objective spinal measurements using the Spinal Mouse device. Functional performance will be assessed using standardized tests such as the 6-minute walk test and the timed up and go test. Statistical analysis will include correlation and regression models to determine whether spinal alignment parameters can predict functional outcomes. The findings are expected to provide insight into the biomechanical role of posture in functional recovery among individuals with upper cross syndrome.

Eligibility

Sex
MALE
Min age
20 Years
Max age
29 Years
Healthy volunteers
No
Inclusion Criteria: * 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. Exclusion Criteria: * 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

Primary outcome measure(s)

  • Spinal Alignment: Thoracic kyphosis — Pre and post 8 weeks
    Kyphosis is the forward curvature of the thoracic spine.It will be measured by The Spinal Mouse ( a hand-held, computer-assisted medical device used to measure spinal curvature, posture, and segmental mobility without radiation )
  • Spinal Alignment: Lumbar lordosis — Pre and post 8 weeks
    inward curvature of the spine when this curve becomes excessive or diminished, it can lead to discomfort and postural issues.It will be measured by The Spinal Mouse ( a hand-held, computer-assisted medical device used to measure spinal curvature, posture, and segmental mobility without radiation )

Trial sites (1)

FacilityCityRegionStatus
Mohamed Saied Zidan Cairo Egypt Recruiting

More Al-Zaytoonah University of Jordan trials in Egypt

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Clinical Effect of Swedish Massage Versus Adjuvant Yoga on Blood Glucose Level in Children With Type 1 Diabetes Mellitus Active, not recruiting
Water Based Burpee Exercises on Functional Capacity in Poste-menopausal Women After Thyroidectomy Recruiting

Other trials for the same condition

Effect of Respiratory Trainer on Cardiopulmonary Functions in Patients with Upper Cross Syndrome Post-Cardiac Surgery Recruiting
AI Training Program vs Standard Correction for Forward Head and Rounded Shoulder in Neck Pain Active, not recruiting
Dynamic Neuromuscular Stabilization Versus Corrective Exercises in Upper Cross Syndrome Starting soon
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07786415 on ClinicalTrials.gov ↗ ← All trials in Egypt