Intercultural Adaptation and Validation of the "Orebro Musculoskeletal Pain Questionnaire"

Neck Pain Clinical Trial

— Orebro-G  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02540343
• Other study ID #: Balgrist 2013-0394
• Status: Completed
• Phase: N/A
• First received: August 21, 2015
• Last updated: November 3, 2016
• Start date: November 2014
• Est. completion date: October 2016

Study information

• Verified date: November 2016
• Source: Balgrist University Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Ethikkommission
• Study type: Observational

Clinical Trial Summary

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

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 information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: October 2016
• Est. primary completion date: October 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

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 Design

N/A

Related Conditions & MeSH terms

• Musculoskeletal Pain
• Neck Pain

Intervention

Other:
• questionnaires
fill out all questionnaires twice

Locations

Country	Name	City	State
Switzerland	Balgrist University Hospital	Zurich

Sponsors (2)

Lead Sponsor	Collaborator
Balgrist University Hospital	Maastricht University

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Voice Handicap, on the Voice Handicap Index (VHI-9)	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.	No
Other	Movement restriction, on self-reported measurements of the Range of motion of the cervical spine	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.	No
Primary	Pain, on the German Version of the Orebro Musculoskeletal Pain Screening Questionnaire	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.	No
Secondary	Disability, on the Neck Disability Index (NDI-G)	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.	No
Secondary	Pain, on Visual Analogue Pain Rating Scale (VAS)	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.	No