Intercultural Adaptation and Validation of the "Orebro Musculoskeletal Pain Questionnaire" (Orebro-G)

November 3, 2016 updated by: Swanenburg, Balgrist University Hospital

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

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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.

Study Type

Observational

Enrollment (Actual)

90

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

  • Switzerland
      • Zurich, Switzerland, 8008
        • Balgrist University Hospital

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

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Acute and chronic neck pain patients Healthy volunteers

Description

Inclusion Criteria:

Acute:

  • Recently diagnosed with neck pain (< 30 days)
  • Must be able to speak, read and write German

Chronic:

  • 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

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?

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
acute neck pain patients
Participant recently received the diagnosis of neck pain (< 30 days) >18 years old able to speak, read and write German, questionnaires
Other: questionnaires
fill out all questionnaires twice
chronic neck apin patients
Participant has neck pain for a longer period of time (> 90 days) > 18 years old able to speak, read and write German, questionnaires
Other: questionnaires
fill out all questionnaires twice
test persons
no neck pain > 18 years old able to speak, read and write German, questionnaires
Other: questionnaires
fill out all questionnaires twice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
For every patient the average study length is one week.

Secondary Outcome Measures

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

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Voice Handicap, on the Voice Handicap Index (VHI-9)
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.
For every patient the average study length is one week.
Movement restriction, on self-reported measurements of the Range of motion of the cervical spine
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.
For every patient the average study length is one week.

Collaborators and Investigators

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

Sponsor

Balgrist University Hospital

Collaborators

Maastricht University

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.

General Publications

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)

October 1, 2016

Study Completion (Actual)

October 1, 2016

Study Registration Dates

First Submitted

August 21, 2015

First Submitted That Met QC Criteria

September 1, 2015

First Posted (Estimate)

September 3, 2015

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

  • Balgrist 2013-0394

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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