The National Musculoskeletal Audit and Research Database

Musculoskeletal Diseases Clinical Trial

Official title:

Developing and Testing a Musculoskeletal National Audit in Community/Primary Care

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05842915
• Other study ID #: RG-0359-22
• Status: Recruiting
• Start date: July 7, 2023
• Est. completion date: July 7, 2025

Study information

• Verified date: October 2023
• Source: Keele University
• Contact: Roanna Burgess, Dr
• Phone: 01782733900
• Email: r.m.burgess[@]keele.ac.uk
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Developing and testing a musculoskeletal national audit in community/primary care

Description:

This project aims to develop, setup and test an MSK national audit which will use patient and clinician inputted data to measure the quality of care for patients presenting in community MSK services and general practice with common MSK conditions. Secondly this project aims to use the national MSK audit information to understand and improve the quality and consistency of care for MSK patients.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 22000
• Est. completion date: July 7, 2025
• Est. primary completion date: July 7, 2024
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

(MSK Services)

• MSK service seeing adult (+18 years) set in community care
• MSK service with at least 10 WTE HCPs
• System in place for digital collection of PROM/PREM data (FCP Services)
• FCP service seeing adult (+18 years) in primary care
• FCP service with at least 1 WTE FCP seeing MSK patients
• Use of EMIS or SYSTMONE
• Able to implement Midlands FCP template
• System in place for digital collection of PROM/PREM data (For patients)
• +18 years
• Active phone number or verified email address to participate in the patient questionnaire
• Able to provide informed consent Exclusion Criteria: (MSK Services)
• Secondary care MSK services (For patients)
• Has declined for data to be part of research as part of consent process
• Unable to complete surveys due to health issues including severe or terminal illness, severe learning difficulties or psychological disorders

Related Conditions & MeSH terms

• Musculoskeletal Diseases

Intervention

Behavioral:
• Questionnaire
Baseline and 3 month questionnaire

Locations

Country	Name	City	State
United Kingdom	Keele University	Keele	Staffordshire

Sponsors (1)

Lead Sponsor	Collaborator
Keele University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To provide a secure national MSK research database for participating MSK providers to upload their routinely collected data.		12 months
Secondary	To develop a standard dashboard and reporting system that supports an ongoing automated process to analyse and present the data for quality improvement purposes.		12 months