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Search / Trial NCT06978751

Development of a Risk Assessment Tool for Incontinence-associated Dermatitis (IAD): a Cohort Study on the Predictive Performance of Risk Factors for IAD

Launched by ÖREBRO UNIVERSITY, SWEDEN · May 16, 2025

Trial Information

Current as of July 09, 2025

Enrolling by invitation

Keywords

Dermatitis Risk Factors Urinary Incontinence Fecal Incontinence Prognosis

ClinConnect Summary

Problem Statement:

Incontinence-Associated Dermatitis (IAD) is a type of irritant contact dermatitis caused by prolonged skin exposure to urine and/or feces. It commonly affects individuals with incontinence. IAD is associated with decreased quality of life, increased care burden, loss of independence, and higher susceptibility to secondary infections and pressure ulcers. These complications lead to prolonged hospital stays and increased healthcare costs.

Despite its clinical relevance, there is insufficient consensus regarding the most critical risk factors for IAD. Existing literature p...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • The patient or their legally authorized representative signed informed consent.
  • The patient is aged 18 years or older.
  • The patient suffers from incontinence\* (urinary, faecal, double incontinence).
  • The patient is free of IAD at inclusion. \*Incontinence is defined as involuntary loss of urine and/or stool.
  • Exclusion Criteria:
  • Patients admitted to emergency departments, paediatric units, maternity units, psychiatric units, and palliative care units.
  • Patients who are receiving end-of-life care.

About örebro University, Sweden

Örebro University, located in Sweden, is a prominent academic institution dedicated to advancing research and education in various fields, including health sciences. The university actively engages in clinical trials to enhance medical knowledge and improve patient outcomes. With a strong focus on interdisciplinary collaboration, Örebro University fosters innovative research initiatives that align with ethical standards and regulatory requirements. Its commitment to excellence in clinical research is supported by a team of experienced researchers and state-of-the-art facilities, making it a key player in the global medical research community.

Locations

Uppsala, , Sweden

Kortrijk, , Belgium

Ghent, , Belgium

Ghent, , Belgium

Izegem, , Belgium

Rumbeke, , Belgium

Veurne, , Belgium

Patients applied

0 patients applied

Trial Officials

Dimitri Beeckman, Professor, PhD, MSc, RN

Principal Investigator

Swedish Centre for Skin and Wound Research (SCENTR), School of Health Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported