MedPath

Touch and Feel Evaluation of Two Foam Hand Sanitizers

Phase 4
Completed
Conditions
Hand Hygiene
Interventions
Drug: Post-market foam alcohol-based hand sanitizer #1
Drug: Post-market foam alcohol-based hand sanitizer #2
Registration Number
NCT05755282
Lead Sponsor
Medline Industries
Brief Summary

Hand sanitizers are a standard of hygiene requirements. Hand sanitizers must be effective at reducing germ count on the hands while ideally providing emollients to moisturize the skin after use. To improve compliance with hand sanitizing protocols, hand sanitizers should provide a pleasant touch and feel experience for end users, especially for healthcare worker (HCW) users, who use these products frequently.

Detailed Description

Hand sanitizers are a standard of hygiene requirements. Hand sanitizers are a standard tool frequently used in hospital settings by healthcare (HCWs) for hand disinfection. The Centers for Disease Control and Prevention (CDC) states that HCWs should use an alcohol-based hand rub, such as a hand sanitizer, or wash their hands with soap and water immediately before and after patient contact, during aseptic tasks, after contact with blood, bodily fluids, or contaminated surfaces, and immediately after glove removal. 1 Additionally, the World Health Organization (WHO) guidelines on hand hygiene state that alcohol-based handrubs rapidly and effectively inactivate a wide array of potentially harmful microorganisms on hands. 2 Hand sanitizers must be effective at reducing germ count on the hands while ideally providing emollients to moisturize the skin after use. To improve compliance with hand sanitizing protocols, hand sanitizers should provide a pleasant touch and feel experience for users, especially for healthcare worker (HCW) users.

The goal of this study is to evaluate the user touch and feel experience of two hand sanitizer foam products produced by Medline and GOJO when the products are used by HCWs.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
46
Inclusion Criteria
  • Healthcare workers ≥ 18 years of age
Exclusion Criteria
  • Individual has a skin condition that might result in irritation from the hand sanitizers.
  • Individual has a known allergy to the ingredients in the test products.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
A: spectrum first then PurellPost-market foam alcohol-based hand sanitizer #1Half of participants will apply Spectrum Advanced (#1) Hand Sanitizer Foam followed by Purell Advanced (#2) Hand Sanitizer Foam
A: spectrum first then PurellPost-market foam alcohol-based hand sanitizer #2Half of participants will apply Spectrum Advanced (#1) Hand Sanitizer Foam followed by Purell Advanced (#2) Hand Sanitizer Foam
B: Purell first then spectrumPost-market foam alcohol-based hand sanitizer #1Half of participants will apply hand Purell Advanced (#2) Hand Sanitizer Foam followed by Spectrum Advanced (#1) Hand Sanitizer
B: Purell first then spectrumPost-market foam alcohol-based hand sanitizer #2Half of participants will apply hand Purell Advanced (#2) Hand Sanitizer Foam followed by Spectrum Advanced (#1) Hand Sanitizer
Primary Outcome Measures
NameTimeMethod
Primary Objective Foam Sanitizer User Touch and Feel Experienceup to 30 mins to complete on a single day; Directly after participants hands have dried after application of each hand sanitizer product

The user touch and feel experience of the foam hand sanitizer products evaluated by visual analog scale assessments (VAS) ranging from 0 to 100, with higher scores indicating a more favorable outcome, of healthcare workers overall satisfaction and moisturization.

Primary Objective Foam Sanitizer User Preferenceup to 30 mins to complete on a single day; Directly after both products had been applied and washed off.

Healthcare workers' assessment of foam product preference via questionnaire, this was asked "and this question was asked after both \*products\* had been applied and washed off"

Primary Objective Foam Sanitizer User Preference 2up to 30 mins to complete on a single day; Directly after both products had been applied and washed off.

Participants were asked "If the other product was chosen by the facility, I would object". this was asked in the time window after both products had already been applied and washed off and therefore this question has a different arms grouping than the first set of questions. It was not asked when a given product was on the skin. The participants were blinded to the product being tested at a given time -- so there was no intent to connect this question to the product testing. The facility had clearly labeled wall units with hand sanitizer and all nurses were aware of what brand of product hand sanitizer the facility used.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

NorthShore University HealthSystem

🇺🇸

Evanston, Illinois, United States

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