Improving pathways for wrist injury treatment
Improving Wrist Injury Pathways (I-WIP): a Qualitative Study
This study is looking to see if getting MRI scans sooner for people with wrist injuries that look normal on x-rays can help them recover faster and make better use of NHS resources.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 70 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Oxford Academic / other |
| Locations | 1 site (Oxford, Oxon) |
| Trial ID | NCT05835440 on ClinicalTrials.gov |
What this trial studies
This observational study aims to address the implementation gap in the use of MRI scans for patients with wrist injuries that appear normal on x-rays. It highlights the importance of early MRI scans as recommended by NICE guidelines, which can lead to quicker recovery for patients and more efficient use of NHS resources. The study will investigate the reasons behind the underutilization of MRI scans in clinical practice and seek to develop effective interventions to improve adherence to these guidelines. By engaging both patients and NHS staff, the study aims to gather insights that could enhance the management of wrist injuries.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old who are being treated for a traumatic wrist injury with a normal initial x-ray.
Not a fit: Patients with learning difficulties may not benefit from this study due to challenges in providing informed consent.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment pathways for patients with wrist injuries, ensuring they receive timely and appropriate care.
How similar studies have performed: While the study addresses a known gap in clinical practice, it is based on established guidelines and aims to improve adherence rather than testing a novel treatment approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria - All participants are willing and able to give informed consent for participation in the study (including audio recording of interview). Where possible we shall use translation services to enable those who might not adequately understand various forms of information to take part For staff stakeholders (NHS staff) - Any staff member involved in regular delivery or management of Wrist Injury Pathways (e.g. manager, nurse practitioner, physiotherapist, surgeon, administrative staff, radiologist, radiographer, emergency department clinician). This staff member must be deemed to be integral in the day to day running and/or overall management of the pathway. For patients: * Male or female aged over 18 years of age * Being treated for a traumatic wrist injury with a normal initial X-ray Exclusion Criteria - Learning difficulty
Where this trial is running
Oxford, Oxon
- OUH NHS TRust — Oxford, Oxon, United Kingdom (Recruiting)
Study contacts
- Study coordinator: Gail Lang
- Email: gail.lang@ndorms.ox.ac.uk
- Phone: 01865741155
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.