MACHO: Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT03987178
Collaborator
(none)
36
1
2
10
3.6

Study Details

Study Description

Brief Summary

The purpose of this study is to determine if there are microbiologic alterations of the ocular surface after hot tub exposure. The study will evaluate the number of microbes before and after hot tub use in order to find out whether hot tub exposure has any change on the organisms present on the ocular surface. Participants will be randomized to dunk or not to dunk their head during their time in the hot tub.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Dunk
  • Other: Exposure to Hot Tub
N/A

Detailed Description

Keratitis is a rare destructive cause of blindness. It typically affects young and healthy individuals, is excruciatingly painful, and difficult to treat. With 60% of cases mis-diagnosed at presentation, acanthamoeba keratitis carries a far worse visual prognosis compared to other cornea infections. Exposure to hot tubs is a widely accepted risk factor. However, the mechanism of infection and prediction of who is at risk is unknown as the vast majority of hot tub users do not become infected.In vivo changes to ocular microbiology after hot tub exposure has never been described.

Changes to ocular microbiology after exposure to hot tubs have not been described. The purpose of this study is to investigate whether there are significant alterations in the microbiology of the conjunctiva after hot tub exposure that may contribute to these changes.

This study will recruit at least 34 subjects, who will be randomized to head submersion versus no head submersion, using at least three different hot tubs. A conjunctival swab, a minimal-risk test performed routinely in the eye clinic, will be performed before and after 15 minutes of hot tub exposure on one eye (randomized) per subject. The swabs will be plated on blood agar (bacterial cultures) and non-nutrient agar (acanthamoeba cultures).

In this prospective study, healthy subjects will be recruited. The study will be Health Insurance Portability and Accountability Act compliant and approved by the Institutional Review Board. All subjects will review and sign an informed consent form.

Each patient will have the conjunctiva of one eye (randomized) cultured. This practically no-risk technique entails touching a polyester-tip swab to the lining of the lower eyelid. Each subject will be randomized to head submersion or no head submersion; this exposure will be masked by the study coordinator. After 15 minutes of hot tub exposure, the subject will have the same eye swabbed for cultures.

Each sample (pre- and post-hot tub) will be randomly assigned a study number. One study coordinator will record and mask data. Water from each tub will be cultured.

The culture plates will be sent to our microbiology facility at UCSF and identification of organisms on the blood agar plates will be performed on our MALDI (mass spectrometry to identify bacteria and fungi). Non-nutrient agar plates will be plated with E. coli overlay and incubated for up to 7 days. The plates will be randomized and the microbiologists will be masked to exposures.

Study Design

Study Type:
Interventional
Actual Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
A provider is assigned to perform conjunctival swabs; this person is completely masked to exposure. The culture plates, which are randomized, are sent to a microbiology lab and the technicians are completely masked to exposures when reading the plates.
Primary Purpose:
Prevention
Official Title:
Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists
Actual Study Start Date :
May 27, 2019
Actual Primary Completion Date :
Mar 26, 2020
Actual Study Completion Date :
Mar 26, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Head Dunk

Subjects who are assigned to be in this arm are asked to sit in a hot tub for 15 minutes and instructed to submerge his or her head in the hot tub at least once and at least up to the eyebrows during his or her time in the hot tub.

Behavioral: Dunk
If randomized to "Dunk," the subject is asked to submerge his or her head in the hot tub at least up to brow level.

Other: Exposure to Hot Tub
Subjects will be asked to sit in a hot tub for 15 minutes (with an individual timer).

Placebo Comparator: No Head Dunk

Subjects assigned to this arm are asked to sit in a hot tub for 15 minutes but to keep his or her chin above water during the entire time.

Other: Exposure to Hot Tub
Subjects will be asked to sit in a hot tub for 15 minutes (with an individual timer).

Outcome Measures

Primary Outcome Measures

  1. Quantity of organisms [1 year]

    Genus-species will be identified for each sample, and quantified with an ordinal scale (0-4). The total of this score will be the quantity for that person-time. The primary analyses will be a Wilcoxon Rank Sum test (Mann-Whitney) between the two arms at the follow-up time point (randomized comparison of dunk vs no-dunk), and a Wilcoxon Signed Rank test between pre-hot-tub and post-hot-tub (longitudinal comparison of all cases). We estimate that a total of 20 subjects will provide 80% power to detect a 1.25 SD difference in the total quantity score between randomization arms at the post (f/u) time point. We estimate 80% power to detect a .9 SD difference between pre (baseline) and post (f/u) time points in a paired longitudinal analysis.

Secondary Outcome Measures

  1. Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (post-test comparison) [1 year]

    The investigators will assess whether organism diversity (richness) changes between arms (post-test comparison) using Simpson's Diversity, expressed in units of effective number (see Jost). We will also assess using Shannon's Diversity.

  2. Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (pre versus post) [1 year]

    The investigators will assess whether organism diversity (richness) changes longitudinally (pre vs post-test comparison).

  3. Difference in organism profile with hot tub use (pre versus post) [1 year]

    The investigators will determine whether the organism profile differs longitudinally (pre vs post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)

  4. Difference in organism profile with hot tub use (between arms) [1 year]

    The investigators will determine whether the organism profile differs between arms (post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)

  5. Quantity comparing pre-hot tub and post-hot tub swabs [1 year]

    We will compare quantity of organisms (amount and type) before and after hot tub use in both arms. We will used a paired t-test for analysis.

  6. Specific organisms found in the conjunctiva with hot tub use [1 year]

    The investigators will compare specific organisms (Staphylococcus epidermidis, Corynebacterium species) between arms (post-test only) and longitudinally between time points (pre vs post-test) with Bonferroni correction

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion criteria:
  • greater of 18 years of age

  • a willing participant

  • healthy

Exclusion criteria:
  • pregnancy

  • high or low blood pressure

  • active diarrhea

  • lymphedema

  • heart disease

  • seizure disorder.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCSF San Francisco California United States 94122

Sponsors and Collaborators

  • University of California, San Francisco

Investigators

  • Principal Investigator: Gerami D Seitzman, MD, UCSF/Proctor Foundation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT03987178
Other Study ID Numbers:
  • 18-26141
First Posted:
Jun 14, 2019
Last Update Posted:
Sep 10, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of California, San Francisco
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 10, 2020