Treatment of Incontinence Associated Dermatitis - Automated

Dermatitis Clinical Trial

— TRIAD-A  

Official title:

Treatment of Incontinence Associated Dermatitis - Automated

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03046810
• Other study ID #: SC-01
• Status: Recruiting
• Phase: N/A
• Start date: April 1, 2017
• Est. completion date: September 2019

Study information

• Verified date: May 2018
• Source: SchwabCare
• Contact: Jacqueline Silvia
• Phone: +1 (855) 239-2106
• Email: jsilvia[@]schwabcare.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Incontinence and the skin irritation (dermatitis) associated with it are common problems. Treatment of dermatitis is effective, but requires effective cleaning and application of a barrier substance to prevent further contact between urine or feces and the skin. Water based cleansing with the addition of a pH balanced cleanser is more effective than standard abrasive cleansing with paper or a cloth, and is better tolerated by those with skin irritation. Zinc oxide based barriers effectively promote healing and prevent further skin damage. Spray forms are less cumbersome and generally preferred, but are difficult to for the patient to apply independently given the challenge of accessing the perineum.

40 patients, recruited from 3 specialty pelvic floor centers and 1 assisted living center will be provided a device that cleans, dries, and applies zinc oxide barrier spray with each use of the toilet. Dermatitis will be evaluated at the beginning of the study, and at weeks 1, 2 and 6 by medical staff using a standard scale (The Kennedy Scale).Quality of life will be measured using a visual analog scale derived from the quality of life in incontinence scale.

The investigators hypothesize that the device will 1) effectively treat incontinence associated dermatitis, 2) prevent recurrence, and 3) be preferred over standard treatment.

Description:

Incontinence and incontinence associated dermatitis (IAD) are common problems. A recent CDC study noted that up to 50% of noninstitutionalized patients aged 65 and older experienced episodes of incontinence at least monthly, and that 40% of those with incontinence develop secondary IAD The treatment of IAD is focused on effective cleaning and prevention of further exposure to irritant liquids and solids through barrier creams. Enzymatic washes have proven efficacy over soap and water, and zinc oxide is the standard of care for barrier function. Combined, effective cleansing and barrier use treats IAD in as little as 6 days, and effectively prevents recurrent skin damage. In one study, an effective preventive regimen of regularly applied skin therapy reduced the incidence of IAD in an at risk population from 25% to 5%. The combination of enzymatic skin cleanser and barrier protection is the standard of care for maintenance of skin integrity in patients with chronic urinary and fecal incontinence.

Adherence to prescribed regimens is a major barrier to regular use of substances applied to the perineum. Difficulty in accessing the perineum make adherence challenging to those with both full and limited mobility, often requiring assistance from a caregiver. The associated loss of independence and dignity are major detriments to quality of life. Novel formulations of zinc oxide, using aerosol based spray application, facilitate use and improve patient acceptance. In a 2014 nursing home based industry study, spray based zinc oxide was preferred by 80% of patients and caregivers, and improved treatment and prevention of IAD in 70% of the study participants.

Adequate cleansing and drying prior to the application of barrier products is key to effective prevention of skin breakdown. Water-based cleaning of the perineum after toileting has been demonstrated to improve hygiene over standard mechanical, paper-based cleansing, especially in those with limited mobility or incontinence. Evidence further demonstrates that the addition of pH balanced cleansers, applied without mechanical abrasion from cloths or wipes, advances hygiene and minimizes risk of secondary infection.

Study Aims

The aims of this study are to evaluate the efficacy of an automated delivery system for cleansing the perineum, and applying zinc oxide barrier spray to effectively treat and prevent incontinence associated dermatitis in a population with active or recurrent IAD. Secondary aims will be to assess preference for the automated delivery system over standard wash and manually applied barrier sprays.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: September 2019
• Est. primary completion date: July 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Ability to give informed consent.

• Active functional urinary or fecal incontinence

• Kennedy Scale Grade >2 with active incontinence associated dermatitis

• Willingness to have device installed in home/care center

Exclusion Criteria:

• Active perineal infection

• Prior pelvic radiation

• Perineal surgery within the prior 6 months

• Known allergy or sensitivity to applied agents

• Treatment for dermatitis within the prior 2 weeks.

• Pre-existing pressure ulcer stage 2-4

• Weight exceeding 300 pounds

• Known allergy or hypersensitivity to cleanser or zinc oxide barrier spray

• Home bathroom needs excessive upgrades, or needs ownership authorization

Related Conditions & MeSH terms

• Dermatitis
• Enuresis
• Fecal Incontinence
• Incontinence, Fecal
• Incontinence, Urinary
• Urinary Incontinence

Intervention

Device:
• Wellness toileting system
This group will use the wash, dry, cleanse, and apply zinc oxide barrier spray routinely for all toileting.

Locations

Country	Name	City	State
United States	Skyline Urology	Torrance	California

Sponsors (1)

Lead Sponsor	Collaborator
SchwabCare

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Treatment of dermatitis	Improvement in the Kennedy Score for Dermatitis	6 weeks
Secondary	Prevention of recurrent dermatitis	prevention of recurrent dermatitis by clinical criteria	12 weeks
Secondary	Improvement in quality of life	Assessed by visual analog scale derived from quality of life in incontinence scale	12 weeks