Developing and testing a way to correctly identify people with chronic pain from their primary care records
- Conditions
- Chronic painMusculoskeletal Diseases
- Registration Number
- ISRCTN37628569
- Lead Sponsor
- niversity of Dundee
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 3264
Phase A. Selection of medical records for review from SPIRE participants
1. 18 years of age or over
2. Electronic medical record held by SPIRE-enabled GP practice
Phase B. Invited to complete pain questionnaires
1. 18 years of age or over
2. Capable of providing informed consent
3. Able to communicate in English
4. Person registered with participating GP practice
Phase C. Invitation to a semi-structured interview or focus group discussion(s)
1. 18 years of age or over
2. Capable of providing informed consent
3. Able to communicate in English
4. Patient of a participating GP practice (and who has returned a survey with consent for contact) or practice staff responsible for coding
Phase D: SIRE Report
1. 18 years of age or over
2. Registered with one of the 6 GP practices involved in the study.
3. Patient has not opted out of SPIRE
Phase A. Selection of medical records for review
1. Under 18 years of age
2. Patient has opted out of SPIRE
Phase B. Invited to complete pain questionnaires
1. Under 18 years of age
2. Not capable of providing informed consent
3. Unable to communicate in English
4. GP does not deem patient suitable for inclusion
5. Patient has opted out of SPIRE
Phase C. Invitation to a semi-structured interview or focus group discussion
1. Under 18 years of age
2. Not capable of providing informed consent
3. Unable to communicate in English
4. GP does not deem patient suitable for inclusion
5. Patient has opted out of SPIRE
6. Not patient of a participating GP practice or not a member of staff in a GP practice
Phase D:
1. Under 18 years of age
2. Patient has opted out of SPIRE
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method