Neck Pain Clinical Trial
Official title:
Cervical Range of Motion in Neck Pain Patients: A Mixed Methods Study
Verified date | May 2017 |
Source | Balgrist University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study there are any associations between objective and subjective outcome measures, measuring the cervical range of motion and if the restriction matter to the patient.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 2017 |
Est. primary completion date | April 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with any duration of neck pain - Men and women older than 18 years - Signed informed consent Exclusion Criteria: - Disc herniation of the cervical spine - Spinal canal stenosis - Acute accidents - Surgery of the cervical spine - Pacemaker and / or defibrillator |
Country | Name | City | State |
---|---|---|---|
Switzerland | Balgrist University Hospital | Zurich |
Lead Sponsor | Collaborator |
---|---|
Balgrist University Hospital | Maastricht University |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cervical Range of Motion (CROM) | The cervical range of motion will be measured using the CROM device | Baseline | |
Secondary | Neck Disability Index | Questionnaire, measuring the subjective restriction of the participant during activities of daily living | Baseline | |
Secondary | S-ROM-Neck | Questionnaire, the participants will be asked to assess their ability to move there neck and if they feel restricted. | Baseline | |
Secondary | Interviews (personal,semi-structured guided, open-ended questions) in a one-to-one Setting. Recorded with a voice-recorder. | 10 of the participants will be asked to also take part in an interview. | Baseline |
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