Functional Performance, Spinal Alignment, Upper Cross Syndrome
Conditions
Keywords
upper cross syndrome, Spinal alignment, Functional performance
Brief 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.
Interventions
OTHERThe 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
OTHERcontrol 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
Sponsors
Al-Zaytoonah University of Jordan
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
MALE
Age
20 Years to 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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 ) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Functional Performance: 6-Minute Walk Test (6MWT) | Pre and post 8 weeks | a clinical exercise test that measures the total distance an individual can walk on a flat, hard surface over a period of 6 minutes |
| Functional Performance: Timed Up and Go Test (TUG) | Pre and post 8 weeks | measures functional mobility and fall risk. It records the seconds it takes a person to stand up from a standard armchair, walk 3 meters (10 feet), turn around, walk back, and sit down again |
Outcome results
None listed