CompletedNot Applicable

Effect of Neural Mobilization in Upper Cross Syndrome

Egypt60 participantsStarted 2025-06-10

Plain-language summary

The purpose of this study is to investigate the effect of Neural Mobilization in patients with Upper Cross Syndrome.

Who can participate

Age range

20 Years – 50 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age ranged from 20 to 50 years. * Body Mass Index ≤30 kg/m². * All participants have a forward head, craniovertebral angle \< 50°. * All participants have round back (kyphosis angle ≥ 42°). * All participants have rounded shoulders of ≥ 52°. * The subjects were chosen from both genders based on an assessment of upper cross syndrome by photogrammetric analysis. * All participants have pain intensity level measured by visual analogue scale (4-8). * All participants tested positive for upper limb tension test of median nerve. Exclusion Criteria: * History of trauma or surgery in the cervical region. * Bone fractures or acute soft tissue injuries. * Osteoporosis. * Pregnant women. * Cancer. * Neurological conditions affecting cervical and thoracic spine. * Connective tissue disease: This includes diseases such as osteomyelitis, lupus, and scleroderma.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Forward head angle

Timeframe: 6 weeks

Rounded shoulder angle

Timeframe: 6 weeks

Kyphosis angle

Timeframe: 6 weeks

Trial details

NCT IDNCT07017738

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-10

View on ClinicalTrials.gov More Upper Cross Syndrome trials

Who can participate

Age range

20 Years – 50 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.