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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age20-29
SponsorAl-Zaytoonah University of Jordan

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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).

Trial design

Design model

Parallel

Treatments tested in this trial

  • The experimental group will perform ujjayi pranayama and osteopathic manipulative tratment

    Other intervention

    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

    Other intervention

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

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Experimental groupExperimental treatment 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Spinal Alignment: Thoracic kyphosis

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 )

Time frame
Pre and post 8 weeks
2

Spinal Alignment: Lumbar lordosis

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 )

Time frame
Pre and post 8 weeks

Secondary outcomes

1

Functional Performance: 6-Minute Walk Test (6MWT)

a clinical exercise test that measures the total distance an individual can walk on a flat, hard surface over a period of 6 minutes

Time frame
Pre and post 8 weeks
2

Functional Performance: Timed Up and Go Test (TUG)

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

Time frame
Pre and post 8 weeks

Other outcomes

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