Unilateral Blindness/ Unilateral Deafness-relation to Neck Pain

March 21, 2013 updated by: Lemberg Hadas, Hadassah Medical Organization

Neck pain is a common complaint in the general population affecting 10-15% of the general population. females more than men. Known risk factors are: Trauma, Repetitive lifting of heavy objects at work, driving vibrating vehicles, frequents diving from boards and smoking. No study dealt with the possible role of unilateral loss of vision or hearing as a risk factor for the development of neck pain. Intuitively, one might suspect that unilateral blindness or deafness will lead to a tilted position of the head, in order to cover a better visual/audio field. This position, in time, might lead to the development of neck pain.

Our hypothesis is that patients with unilateral blindness/deafness will suffer from neck pain more frequently than the general population.

Study Overview

Status

Terminated

Study Type

Observational

Enrollment (Anticipated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Jerusalem, Israel
        • Hadassah Medical Organization.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 year to 65 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

study group: patients with unilateral blindness and unilateral deafness as the control group: patients attending the eye ENT clinics for other reasons as control

Description

Inclusion criteria:

  • Men and women suffering from unilateral blindness or deafness
  • Men and women visiting the ophthalmology or ENT clinics (general population) for reasons other than unilateral blindness/deafness and agreeing to participate in the study.
  • Over 18 years of age
  • Signed informed consent

Exclusion criteria:

  • Subjects suffering from neck pain as a result of fractures, infection, or metastatic disease.
  • Inability to understand or fill out the questionnaire/informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
neck pain
Time Frame: two weeks
two weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yair Barzilay, Hadassah Medical Organization

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted

December 23, 2007

First Submitted That Met QC Criteria

December 23, 2007

First Posted (Estimate)

January 9, 2008

Study Record Updates

Last Update Posted (Estimate)

March 22, 2013

Last Update Submitted That Met QC Criteria

March 21, 2013

Last Verified

March 1, 2013

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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