Skip to main content
Clinical Trials/NCT02540343
NCT02540343
Completed
N/A

Intercultural Adaptation and Validation of the "Orebro Musculoskeletal Pain Questionnaire"-Translation and Validation of a Questionnaire

Balgrist University Hospital1 site in 1 country90 target enrollmentNovember 2014
ConditionsNeck Pain

Overview

Phase
N/A
Intervention
Not specified
Conditions
Neck Pain
Sponsor
Balgrist University Hospital
Enrollment
90
Locations
1
Primary Endpoint
Pain, on the German Version of the Orebro Musculoskeletal Pain Screening Questionnaire
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The aim of this study is to adapt and translate the Orebro Musculoskeletal Pain Questionnaire into German.

Detailed Description

Participants will fill out all questionnaires at baseline and again after three days. If the questionnaires have not been returned by day four the participant receives a reminder telephone call. Patients that do not return the questionnaires by day seven are dismissed. The baseline measurement is done at the practice the second measurement will be done by the patient at home. To send the questionnaire back the participant receives a prepaid envelope.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
October 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Balgrist University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Swanenburg

PhD

Balgrist University Hospital

Eligibility Criteria

Inclusion Criteria

  • Recently diagnosed with neck pain (\< 30 days)
  • Must be able to speak, read and write German
  • Neck problems for a longer period of time (\> 90 days)
  • Must be able to speak, read and write German
  • Healthy volunteers:
  • No neck pain
  • Must be able to speak, read and write German

Exclusion Criteria

  • Does not speak, read and write German
  • "Red Flags" e.g. acute trauma
  • Medical knowledge

Outcomes

Primary Outcomes

Pain, on the German Version of the Orebro Musculoskeletal Pain Screening Questionnaire

Time Frame: For every patient the average study length is one week.

Participants are asked to fill out the questionnaire twice. At the start and three to seven days after the first time.

Secondary Outcomes

  • Pain, on Visual Analogue Pain Rating Scale (VAS)(For every patient the average study length is one week.)
  • Disability, on the Neck Disability Index (NDI-G)(For every patient the average study length is one week.)

Study Sites (1)

Loading locations...

Similar Trials