NCT07018219

Brief Summary

detect accuracy of that procedure in identification the seventh cervical vertebra, we aimed to determine accuracy of identification of the seventh cervical vertebra by palpation with neck rotation and side bending in patients with neck pain.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
25

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

May 3, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 4, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 12, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2025

Completed
Last Updated

June 12, 2025

Status Verified

April 1, 2025

Enrollment Period

3 months

First QC Date

June 4, 2025

Last Update Submit

June 4, 2025

Conditions

Keywords

Seventh Cervical vertebra

Outcome Measures

Primary Outcomes (1)

  • The accuracy of palpation technique

    The accuracy of palpation technique will be calculated as the proportion of patients in which the palpated vertebral level corresponded to the radiographic vertebral level.

    2 month

Study Arms (1)

one expermental group:

EXPERIMENTAL

The researcher will detect the seventh cervical vertebrae by palpation with neck Rotation and side bending in patients with neck pain , then patients will be refereed to perform X ray which is the gold standard for detecting C7

Device: X ray device

Interventions

X ray macjine : shimadzo corporation ( japan)

one expermental group:

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • neck pain, age (18- 60) male and female

You may not qualify if:

  • with suspected ankylosing spondylitis, previous surgery on the cervical spine or congenital malformation of the cervical region.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Al ahrar teaching hospital

Zagazig, 44511, Egypt

RECRUITING

Central Study Contacts

Eslam Elsayed Shohda, phd, pt

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Physical therapy teaching fellow

Study Record Dates

First Submitted

June 4, 2025

First Posted

June 12, 2025

Study Start

May 3, 2025

Primary Completion

July 20, 2025

Study Completion

July 20, 2025

Last Updated

June 12, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

undetected

Locations