Pain Relief Strategies for Dressing Change in Chronic Wounds
1 other identifier
observational
25
1 country
2
Brief Summary
A small-scale study using interviews to explore patients', carers' and health care professionals' experience of pain relief strategies currently used in UK practice for dressing change in chronic wounds.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2022
Typical duration for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 5, 2022
CompletedFirst Submitted
Initial submission to the registry
May 25, 2022
CompletedFirst Posted
Study publicly available on registry
June 10, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2024
CompletedDecember 4, 2023
June 1, 2023
2.5 years
May 25, 2022
December 1, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To identify what strategies have been used by patients, carers and healthcare professionals to reduce or remove pain associated with dressing changes in chronic wounds.
experiences and strategies will be explored and captured from qualitative data collected from semi-structured interviews
6 months
Eligibility Criteria
Patients registered with a GP practice in England who are living with a chronic wound, informal or private carers for people living with a chronic wound and health care professionals (staff nurses, tissue viability specialists) providing primary or secondary medical care for someone with a chronic wound.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Goole Health Centre
Goole, Yorkshire, DN14 6RU, United Kingdom
Clifton Medical Centre
Rotherham, Yorkshire, S65 1DA, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Richard Cooper, PhD
University of Sheffield
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 25, 2022
First Posted
June 10, 2022
Study Start
April 5, 2022
Primary Completion
September 30, 2024
Study Completion
September 30, 2024
Last Updated
December 4, 2023
Record last verified: 2023-06
Data Sharing
- IPD Sharing
- Will not share