PREVENTion and treatment of incontinence-associated dermatitis through a codesigned manual (PREVENT-IAD): a study protocol for a feasibility cluster randomised controlled trial with a nested process evaluationShow others and affiliations
2024 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 14, no 12, article id e092338
Article in journal (Refereed) Published
Abstract [en]
INTRODUCTION: Incontinence is commonly experienced by adults who receive care support in a residential facility or in their own home. These individuals are at risk of developing incontinence-associated dermatitis (IAD), which is caused by prolonged and repeated exposure of the skin to urine or faeces. An IAD manual was developed providing an evidence-based clinical algorithm and an e-learning training programme for the prevention and treatment of IAD. The aim of the study is to establish the feasibility of conducting a definitive trial to examine the clinical and cost-effectiveness of the IAD manual. The objectives are to assess recruitment and attrition rates, acceptability of the IAD manual and intervention fidelity.
METHODS AND ANALYSIS: A feasibility cluster randomised controlled trial will be conducted in residential nursing homes and in the homes of people receiving formal care support in London and Hampshire, England. A total of six clusters including n=248 participants who are incontinent of urine, or faeces will be included. At each intervention site, care staff will be trained to implement the IAD manual over a 6-month period. Quantitative outcomes include IAD incidence and severity, IAD-related pain, satisfaction with care and mental health. A qualitative evaluation of care staff and care receivers' experiences of participation will be conducted. Rates and proportions of each feasibility outcome will be described informing the sample size estimation for a definitive cluster randomised controlled trial. A thematic analysis of the qualitative data will be guided by a logic model detailing potential factors impacting on both the study methodology and adoption of the IAD manual into routine care.
ETHICS AND DISSEMINATION: The study received the approval of the Queens Square Ethics Committee Health Research Authority 23/LO/036, (Project ID 296167). Results will be disseminated through peer-reviewed open-access journals and international conferences
TRIAL REGISTRATION NUMBER: ISRCTN70866724.
Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2024. Vol. 14, no 12, article id e092338
Keywords [en]
Clinical Trial, DERMATOLOGY, Feasibility Studies, Urinary incontinences, WOUND MANAGEMENT
National Category
Nursing
Identifiers
URN: urn:nbn:se:oru:diva-118157DOI: 10.1136/bmjopen-2024-092338ISI: 001383220600001PubMedID: 39719286Scopus ID: 2-s2.0-85213932498OAI: oai:DiVA.org:oru-118157DiVA, id: diva2:1925697
Note
Study protocol
This study is funded by the NIHR Health Technology Assessment Programme (NIHR128865).
2025-01-092025-01-092025-01-15Bibliographically approved