NCT07215819

Brief Summary

This observational, cross-sectional study investigates the relationship between cervical sagittal alignment parameters, pain-related disability, and body awareness in patients with chronic neck pain. Adult patients aged 18-50 years who present with neck pain lasting at least 3 months and who have undergone a lateral cervical X-ray within the past 3 months will be included. Cervical sagittal parameters will be measured on radiographs, and participants will complete the Neck Disability Index (NDI) and the Fremantle Neck Awareness Questionnaire to evaluate disability and altered body perception.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
76

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 17, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 11, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 2, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

October 14, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2025

Completed
Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

4 months

First QC Date

October 2, 2025

Last Update Submit

March 17, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Neck Disability Index (NDI)

    At baseline

  • Fremantle Neck Awareness Questionnaire (FreNAQ-Neck)

    At baseline

Study Arms (1)

Neck Pain Group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Adults aged 18-60 years with chronic neck pain of at least 3 months' duration will be recruited. Eligible participants must have undergone lateral cervical X-ray imaging within the past 3 months. Both male and female participants will be included. Exclusion criteria are: prior history of cervical trauma or surgery; cervical radiculopathy or previous cervical spine operations; systemic conditions such as diabetes mellitus, inflammatory rheumatic disease, familial hyperlipidemia, malignancy, or fibromyalgia; and presence of known neurological or psychiatric disorders.

You may qualify if:

  • Adults aged 18-600 years (inclusive), women and men
  • Chronic neck pain ≥3 months in duration
  • Lateral cervical X-ray performed within the past 3 months

You may not qualify if:

  • History of cervical spine trauma or surgery
  • Cervical radiculopathy (history or current radicular neck/arm pain)
  • Systemic conditions: diabetes mellitus, inflammatory rheumatic disease, familial hyperlipidemia, malignancy, or fibromyalgia
  • Known neurological or psychiatric disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Prof. Dr. Cemil Taşçıoğlu Şehir Hastanesi

Istanbul, Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor

Study Record Dates

First Submitted

October 2, 2025

First Posted

October 14, 2025

Study Start

February 17, 2025

Primary Completion

June 11, 2025

Study Completion

November 20, 2025

Last Updated

March 19, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared. Only aggregated and anonymized results will be disseminated through scientific publications.

Locations