- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02754934
Development of a Self-administered Neck Mobility Assessment Tool in Chronic Neck Pain Patients.
November 3, 2016 updated by: Swanenburg, Balgrist University Hospital
This study evaluates, if the movement of the cervical spine, assessed via a specific questionnaire by the patient, is a valid and reliable tool and could be used in daily clinical routine.
Study Overview
Detailed Description
Cervical range of motion is a frequently used assessment methods in patients with neck pain.
Although it seems to be used frequently, clinicians still prefer hands-on assessment. Furthermore it is interesting, if cervical range of motion,self-assessed by the patient is a valid and reliable tool.
Study Type
Observational
Enrollment (Actual)
50
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
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-
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Zurich, Switzerland, 8008
- Balgrist University Hospital
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Investigators will include 50 participants with chronic neck pain
Description
Inclusion Criteria:
- Neck pain > 90 days
- Able to speak, read and write German
Exclusion Criteria:
- Red Flags e.g. Fracture of the cervical spine
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 |
Measure Description |
Time Frame |
---|---|---|
Cervical Spine Mobility
Time Frame: Day one of the study
|
Patients will fill out the questionnaire once, at the beginning of the study.
|
Day one of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Visual Analogue Pain Rating Scale
Time Frame: Day one of the study
|
Patients will fill out the questionnaire once, at the beginning of the study.
|
Day one of the study
|
Disability on Neck Disability Index
Time Frame: Day one of the study
|
Patients will fill out the questionnaire once, at the beginning of the study.
|
Day one of the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jaap Swanenburg, PhD, Balgrist University Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 Major Dates
Study Start
November 1, 2014
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
November 1, 2016
Study Registration Dates
First Submitted
April 25, 2016
First Submitted That Met QC Criteria
April 27, 2016
First Posted (Estimate)
April 28, 2016
Study Record Updates
Last Update Posted (Estimate)
November 4, 2016
Last Update Submitted That Met QC Criteria
November 3, 2016
Last Verified
November 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016-00164
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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