Biomechanical Risk Factors of Cervical Pain in Pregnant Women

NCT ID: NCT06741605

Last Updated: 2024-12-19

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

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

116 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-20

Study Completion Date

2025-03-01

Brief Summary

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The purpose of the study is to assess the biomechanical risk factors for neck pain in pregnant women.

Detailed Description

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Neck pain during pregnancy has significant physical, psychological, and social impacts on women's lives. Moreover, the economic burden of neck pain is remarkable and includes treatment costs, reduced productivity, and job-related problems. Untreated neck pain during pregnancy can potentially lead to chronic musculoskeletal problems postpartum.

The significance of the study is based on the concept of "early prediction for early mitigation of the risk and prevention of the onset or progression".

Studies have investigated risk factors for neck pain. However, there is a notable gap in research regarding these factors in pregnant women, especially physical (biomechanical) risk factors, despite the significant biomechanical changes they undergo during pregnancy. This study aims to fill this gap by investigating the relationship between biomechanical risk factors and neck pain in pregnant women.

To our knowledge, this is the first study in which this relationship will be assessed to provide evidence about the biomechanical risk factors for neck pain in pregnant women.

Conditions

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Cervical Pain

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Pregnant women with cervical pain

Pregnant women with cervical pain in their third trimester will be assessed to investigate the relationship between biomechanical risk factors and neck pain in pregnant women.

Intervention Type OTHER

Interventions

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Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Pregnant women in their third trimester suffering from cervical pain.
* They have experienced cervical pain starting during pregnancy.
* They reported no neck pain or neck-related disorders during the previous year and were screened for the absence of cervical pathology during a physical examination.

Exclusion Criteria

* Objective signs of structural pathology on physical examination, including but not limited to shoulder bursitis, impingement, tendonitis, fracture, cervical nerve or disc impairment, radiculopathy, or loss of upper extremity sensory or motor function.
* Acute injury of the neck or shoulders (\<12 weeks before the study).
* History of fibromyalgia or musculoskeletal pain present in more than 4 body regions concurrently.
* Self-reported systemic illness, including cancer, rheumatic, cardiovascular, or neurological disease
* Untreated psychiatric condition
* Previous surgery involving the cervical spine or shoulders
* Uncontrolled hypertension (resting systolic blood pressure \>150 mm Hg, or diastolic blood pressure \>90 mm Hg).
Minimum Eligible Age

20 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Doaa Ahmed Ibrahim Fadel

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hossam Hussien, Professor

Role: STUDY_DIRECTOR

Al-Azhar University

Doaa Osman, Professor

Role: STUDY_CHAIR

Cairo University

Locations

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Doaa Ahmed Fadel

Zagazig, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Doaa Fadel, Master

Role: CONTACT

Phone: +201013791440

Email: [email protected]

Amira Nagy, PHD

Role: CONTACT

Phone: +201021177871

Email: [email protected]

Other Identifiers

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P.T.REC/012/005381

Identifier Type: -

Identifier Source: org_study_id