Correlation Between Forward Head Posture and Cervical Radiculopathy

NCT ID: NCT07031310

Last Updated: 2025-08-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-07-01

Study Completion Date

2025-12-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The progression rate of forward head posture has increased because of the increase in postural loads, to which individuals are subjected because of developed technologies including mobile phones, computers, and televisions. Postural abnormality in the upper cervical region has the potential to lead to nerve irritation and cervical radiculopathy. so the purpose of study is to investigate if there is a relationship between forward head posture and cervical radiculopathy in smart phone users.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Cross-sectional observational study . 120 Participants will be recruited from students and employees of Nahda university (smart phone users) from both genders with age ranged between (18-35) years old.

outcomes measurement

1. Photogrammetric method to assess CVA by smart phone application FHP
2. Smartphone application for measuring cervical range of motion
3. Numerical Pain Rating Scale to assess pain intensity
4. Arabic neck disability index for measuring cervical function

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Smart Phone Users

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

smart phone users

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

\- 1. Adult subjects aged from 18-35 years old, with FHP using smart phone more than 4 hours per day.

2\. Subjects with FHP (craniovertebral angle) \[CVA\] \< 49° 3. Normal body mass index (BMI \<25).

Exclusion Criteria

\- 1- Signs of serious pathology (e.g., malignancy, inflammatory disorders, infection).

2- History of cervical spine surgery. 3- History of trauma or fractures in cervical spine. 4- Vascular syndrome such as vertebrobasilar insufficiency.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Doaa Rafat

Assistant professor of physical therapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Soheir Shehata Rizkalla, Professor

Role: STUDY_CHAIR

Department of Basic sciences for physical therapy, Faculty of Physical Therapy , Cairo university, Cairo, Egypt

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of Physical Therapy, Nahda University.

Bani-Suef, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

P.T.REC/025/00087

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Upper Cross Syndrome and Neck Proprioception
NCT06801613 NOT_YET_RECRUITING