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Adhesive Tape Placement on Patients' Masks in the Emergency Department Increases Compliance of Proper Face Mask Use

Adhesive Tape Placement on Patients' Masks in the Emergency Department Increases Compliance of Proper Face Mask Use

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04812184
Enrollment
123
Registered
2021-03-23
Start date
2020-04-01
Completion date
2020-10-30
Last updated
2022-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Brief summary

Methods 123 patients were enrolled in a randomized controlled trial at Eskenazi Hospital from April 2020 until October 2020. We permitted patients to either use their own mask (due to low resources institutionally) or we provided a surgical/cloth mask (early on relied on donated cloth masks for patients). Patients were randomized to a control (no tape over the mask/nose) or to the intervention (placing tape over the bridge of the nose of the face mask). Patients were evaluated at 30- and 60- minute intervals to assess for proper mask usage.

Detailed description

Study Design and Setting: This study is a randomized control trial at Eskenazi Hospital ED from April 2020 until October 2020. Eskenazi Hospital is a busy, urban, academic hospital, level 1 trauma center, in downtown Indianapolis. Here we serve a racially diverse, underserved population, with over 100,000 annual ED visits. This work was approved by the Indiana University Institutional Review Board (protocol #2004425945). Selection of Participants: All patients presenting to the ED were screened for enrollment in this study by trained research personnel. All patients are required to wear facial coverings while in the ED, and after screening patients based on the exclusion criteria provided below, patients were offered enrollment in the study. Patients were randomly identified by their bed location in the ED via a random number generator. Patients were excluded from the study for: (1) pregnant; (2) prisoner; (3) not English or Spanish speaking (currently a large cohort of ethnic Latino/Latina/Hispanic are utilizing the ED and we can use interpreters to interpret for enrollment); (4) intoxicated or decompensated psychiatric illness; (5) presenting to the ED with a life-threatening condition; (6) allergic to standard tape and/or tegaderm. Patient consent was obtained if an individual agreed to participate in the study. Interventions: All patients included in this study were approached and offered enrollment in a study for addressing PPE. The control arm consisted of no active intervention, with the treatment arm placing standard surgical tape over the bridge of the nose to adhere the top of the mask to the bridge of the nose, thereby creating a physical barrier from removing the mask from the face. Patients were reevaluated at 30 minutes and 60 minutes after enrollment to assess for proper mask compliance. Measurements: Assuming 50% current compliance, 58 patients per arm were needed to have an 80% power to detect a 25% difference assuming a two-sided chi-square test and alpha = 0.05. Outcomes: The primary outcome of this trial is proper mask utilization upon reevaluation at 30 and 60 minutes, with the mask at/under the chin, meanwhile completely covering the mouth and nose). Secondary outcomes of this trial were comparing the primary demographic and visit related covariates on initial screening, including age, sex, race/ethnicity, past medical history, social history, chief complaint, and disposition (admission vs. discharge). Analysis: Patient demographics and characteristics were compared between the control and treatment groups. To test for differences between groups, Microsoft excel statistical package was utilized, and the Chi-square test was used for categorical variables and the Wilcoxon test for continuous variables.

Interventions

DEVICETape Face Mask

Adding tape to face mask

Sponsors

Indiana University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* presenting to the emergency department during the covid-19 pandemic * older than 18 years of age

Exclusion criteria

* pregnant * prisoner * not english speaking * not intoxicated or decompensated psychiatric illness * not critically ill * not allergic to standard tape and/or tegaderm

Design outcomes

Primary

MeasureTime frameDescription
Proper Face Mask Use up to 60 Minutes60 minutes on Day 1The primary outcome of this trial is proper mask utilization upon reevaluation up to 60 minutes (with the mask at/under the chin, meanwhile completely covering the mouth and nose). At these time point a trained observer enters the room and observes the patient's face covering and its location on the face (correct, chin exposed, nose exposed, not on at all).

Countries

United States

Participant flow

Recruitment details

Patients presenting to the ED were screened for enrollment by trained research personnel when one of the study authors was working. This study was an open-label randomized control trial at Eskenazi Hospital ED from April 2020 to October 2020.

Participants by arm

ArmCount
Surgical Tape to Bridge of Nose
placed a piece of tape to the bridge of the nose, adhering a face mask to the patient's face Tape Face Mask: Adding tape to face mask
60
Standard of Care
Patients given a mask with no intervention to the mask, unless they had their own mask
63
Total123

Baseline characteristics

CharacteristicStandard of CareSurgical Tape to Bridge of NoseTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
58 Participants3 Participants61 Participants
Age, Categorical
Between 18 and 65 years
5 Participants57 Participants62 Participants
Age, Continuous42 years41 years41 years
mask type
Home mask
46 Participants35 Participants81 Participants
mask type
Provided mask
17 Participants25 Participants42 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
1 Participants2 Participants3 Participants
Race (NIH/OMB)
Black or African American
35 Participants32 Participants67 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants0 Participants3 Participants
Race (NIH/OMB)
White
24 Participants26 Participants50 Participants
Region of Enrollment
United States
63 participants60 participants123 participants
Sex: Female, Male
Female
36 Participants25 Participants61 Participants
Sex: Female, Male
Male
27 Participants35 Participants62 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 600 / 63
other
Total, other adverse events
0 / 600 / 63
serious
Total, serious adverse events
0 / 600 / 63

Outcome results

Primary

Proper Face Mask Use up to 60 Minutes

The primary outcome of this trial is proper mask utilization upon reevaluation up to 60 minutes (with the mask at/under the chin, meanwhile completely covering the mouth and nose). At these time point a trained observer enters the room and observes the patient's face covering and its location on the face (correct, chin exposed, nose exposed, not on at all).

Time frame: 60 minutes on Day 1

Population: Overall number of participants analyzed less than total 123. 2 patients were discharged prior to the 60 minute reevaluation from the standard of care group.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Surgical Tape to Bridge of NoseProper Face Mask Use up to 60 Minutes58 Participants
Standard of CareProper Face Mask Use up to 60 Minutes52 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026