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Intercultural Adaptation and Validation of the Orebro Musculoskeletal Pain Questionnaire

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02540343
Acronym
Orebro-G
Enrollment
90
Registered
2015-09-03
Start date
2014-11-30
Completion date
2016-10-31
Last updated
2016-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

Translation, Validation, Orebro-G

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.

Interventions

OTHERquestionnaires

fill out all questionnaires twice

Sponsors

Maastricht University
CollaboratorOTHER
Balgrist University Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Pain, on the German Version of the Orebro Musculoskeletal Pain Screening QuestionnaireFor 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

MeasureTime frameDescription
Disability, on the Neck Disability Index (NDI-G)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.
Pain, on Visual Analogue Pain Rating Scale (VAS)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.

Other

MeasureTime frameDescription
Voice Handicap, on the Voice Handicap Index (VHI-9)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.
Movement restriction, on self-reported measurements of the Range of motion of the cervical spineFor 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.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026