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Efficacy of A multi-modal Approach in Management of Patients with Upper Crossed Syndrome: A randomized Controlled Trial

Efficacy of A multi-modal Approach in Management of Patients with Upper Crossed Syndrome: A randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202001862833093
Enrollment
40
Registered
2020-01-14
Start date
2019-12-20
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases

Interventions

Group A multimodal approach group
Group B muscle energy technique group

Sponsors

Faculty of physical Therapy Cairo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age ranging from 30 to 60 years old. 2. Male and female. 3. subjects who have weakness in deep neck flexors, serratus anterior, middle and lower trapezius and rhomboid muscles and tightness in upper trapezius, levator scapulae, scallenii, posterior neck and subocciptal muscles, pectoralis major and minor and sternocleidomastoid muscles according to the specialized tests that will be conducted. 4. Subjects complaining of this syndrome for more than 3 months. 5. All participants who will be conscious and cooperative. 6. Subjects who are not receiving medications.

Exclusion criteria

Exclusion criteria: 1. BMI more than 40. 2. age older than 60 or younger than 30 years. 3. History of congenital deformity or surgery in spine or shoulder. 4. Participants will be excluded if their cervical and shoulder angles will be =48°and =52°, respectively as above these values are considered normal. 5. Recent cervical whiplash injury and recent spinal fracture. 6. Osteoporotic subjects and compressive fractures caused by osteoporosis. 7. Marked limitation in shoulder ROM. 8. Leg length discrepancy and functional or structural scoliosis. 9. visual deficits and balance disorders. 10. Pregnancy and subjects with sever comorbid diseases. 11. psychosocial problem and cognitive impairment or inability to understand the scale. 12. Systemic inflammatory diseases. 13. Spinal Tumor and stenosis.

Design outcomes

Primary

MeasureTime frame
craniovertebral angle CVA;Sagittal shoulder angle SSA

Secondary

MeasureTime frame
Pain intensity ;Functional status

Countries

Egypt

Contacts

Public Contacthanaa Kenawy Atta

Lecturer of Basic Science Department Faculty of Physical Therapy Cairo University

h_k90girl@yahoo.com+2001008320656

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026