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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03038139
Other study ID # IRB? pGS- 2016-03- 144
Secondary ID
Status Enrolling by invitation
Phase N/A
First received January 23, 2017
Last updated October 2, 2017
Start date November 2016
Est. completion date June 2018

Study information

Verified date October 2017
Source Dammam University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the changes of spinal muscle activation in cervical, thoracic and lumbar segments for subjects with forward head posture (FHP) after application of two correction programs; a conventional one including cervical and thoracic spine, and a second program involving lumbosacral segment.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 60
Est. completion date June 2018
Est. primary completion date February 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 28 Years
Eligibility Inclusion Criteria:

- adults with craniovertebral angle less than 50?

Exclusion Criteria:

- Participants will be excluded if they have

- congenital spinal deformity such as scoliosis

- spinal conditions such as cervical trauma, fracture, instability of cervical spine, inflammation, infection, or neurological deficit

- a history of surgery at cervical spine or shoulder

- pregnant woman

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cervical exercises
Cervical correction program consist of 3 strengthening and 2 stretching exercises for neck and scapula Lumbosacral correction program consist of strengthening and stretching exercises for lumbar and sacral regions
Lumosacral exercises
Cervical and Lumbosacral correction program Lumbosacral program consist of 2 strengthening and 4 stretching exercises

Locations

Country Name City State
Saudi Arabia Dammam University Dammam Eastern Province
Saudi Arabia Dammam University Dammam

Sponsors (1)

Lead Sponsor Collaborator
Dammam University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of Craniovertebral angle The craniovertebral angle will be measure before and after 4 weeks of applying an exercise program. 4 weeks
Secondary Electromyography The Electromyography will be measure before and after 4 weeks of applying an exercise program. 4 weeks
Secondary Neck Disability Index The neck disability index will be measure before and after 4 weeks of applying an exercise program. 4 weeks
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