Intercultural Adaptation and Validation of the "Orebro Musculoskeletal Pain Questionnaire"
- Conditions
- Neck Pain
- Interventions
- Other: questionnaires
- Registration Number
- NCT02540343
- Lead Sponsor
- Balgrist University Hospital
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 90
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
- Does not speak, read and write German
- "Red Flags" e.g. acute trauma
- Medical knowledge
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description acute neck pain patients questionnaires Participant recently received the diagnosis of neck pain (\< 30 days) \>18 years old able to speak, read and write German, questionnaires chronic neck apin patients questionnaires Participant has neck pain for a longer period of time (\> 90 days) \> 18 years old able to speak, read and write German, questionnaires test persons questionnaires no neck pain \> 18 years old able to speak, read and write German, questionnaires
- Primary Outcome Measures
Name Time Method Pain, on the German Version of the Orebro Musculoskeletal Pain Screening Questionnaire 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 Outcome Measures
Name Time Method 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.
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.
Trial Locations
- Locations (1)
Balgrist University Hospital
🇨ðŸ‡Zurich, Switzerland