Exploring pain relief methods for changing dressings on chronic wounds
Pain Relief Strategies for Dressing Change in Chronic Wounds: Qualitative Interview Stage
This study is talking to patients and caregivers to see what pain relief methods work best for changing dressings on chronic wounds like pressure ulcers and diabetic foot ulcers.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 25 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Sheffield Academic / other |
| Locations | 2 sites (Goole, Yorkshire and 1 other locations) |
| Trial ID | NCT05414916 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather qualitative data through interviews with patients, caregivers, and healthcare professionals regarding their experiences with pain relief strategies during dressing changes for chronic wounds. Chronic wounds, which include pressure ulcers and diabetic foot ulcers, often cause significant pain, particularly during dressing changes. The study seeks to identify current practices and the effectiveness of various pain relief methods used in the UK, highlighting the need for better strategies to manage pain associated with wound care. By understanding these experiences, the research aims to inform future practices and improve patient care.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and over who are living with chronic wounds or are involved in caring for someone with a chronic wound.
Not a fit: Patients who are unable to provide informed consent or communicate in English, as well as those under 18 or with severe mental health issues, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing dressing changes for chronic wounds.
How similar studies have performed: While there is limited recent evidence on pain relief strategies for dressing changes in chronic wounds, previous studies have indicated the importance of addressing pain management in wound care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Living with a chronic wound, informally or privately caring for someone with a chronic wound or providing medical care (e.g. dressing change) for someone with a chronic wound * Ability to give informed consent * Aged aged 18 years or above Exclusion Criteria: * Vulnerable patients (e.g. severe mental illness, learning difficulties, dementia, care home residents) * Inability to provide informed consent * Inability to communicate in English * Not living with a chronic wound, informally or privately caring for someone with a chronic wound or providing medical care (e.g. dressing change) for someone with a chronic wound * Under 18 years of age
Where this trial is running
Goole, Yorkshire and 1 other locations
- Goole Health Centre — Goole, Yorkshire, United Kingdom (Recruiting)
- Clifton Medical Centre — Rotherham, Yorkshire, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Richard Cooper, PhD — University of Sheffield
- Study coordinator: Richard Cooper, PhD
- Email: richard.cooper@sheffield.ac.uk
- Phone: +44 114 222 0768
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.