Skip to main content
OpenTrials
Completed

NCT Number: NCT04136574

Hand Dermatitis in the Care and Hospital Staff

Study of the prevalence and risk factors of occupational dermatitis in the hands of caregivers and hospital staff of the Brest CHRU.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU Brest

Brest, 29609, France

About this study

Monocentric cross-sectional descriptive study by anonymous self-questionnaire designed to evaluate among caregivers and agents hospitals of the CHRU de Brest:

  • the prevalence of occupational hands dermatitis
  • the risk factors for hands dermatitis
  • the clinical description of the hands dermatitis
  • the rates of dermatitis according to hand hygiene practices (soap, hydro-alcoholic solution, associations of the two, wearing gloves ...)
  • the changes in the hygiene practices of caregivers and hospital staff of the University Hospital caused by hand dermatitis.
  • the professional and socio-economic impact of these hands dermatitis
  • the evaluation of the use of care for these hands dermatitis.
  • the assessment of the association of hand dermatitis with a personal or family atopic history.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any caregiver, hospital staff or staff involved incare or stretchering of CHU patients returning tosocioprofessional categories cited in the questionnaire.
  • Major person
  • Participation Agreement

Exclusion criteria

  • Minor person.
  • Administrative Services Staff, Restaurant Staff,technical staff
  • Refusal to participate

Treatment and study plan

Primary outcomes

  1. prevalence of occupational hands dermatitis

    Time frame: Three months (at the end of study)

    prevalence of occupational hands dermatitis among the staff of the Brest CHRU.

Secondary outcomes

  1. Risk Factors for Hand Dermatitis

    Time frame: Three months (at the end of study)

    Risk Factors for Hand Dermatitis in Caregivers and Hospital Workers of the Brest Hospital

  2. Clinical description of the dermatitis of the hands

    Time frame: Three months (at the end of study)

    Clinical description of the dermatitis of the hands of the caregivers and the hospital agents of the CHRU of Brest.

  3. rate of dermatitis according to the hygiene practices

    Time frame: Three months (at the end of study)

    rate of dermatitis according to the hygiene practices of the hands (soap, SHA, combinations of both, wearing gloves ...)

  4. changes in hygiene practices

    Time frame: Three months (at the end of study)

    changes in hygiene practices caregivers and hospital staff of the hospital induced by hands dermatitis

  5. Assessment of the professional and socio-economic impact of hand dermatitis

    Time frame: Three months (at the end of study)

    Assessment of the professional and socio-economic impact of hand dermatitis in the care and hospital staff of the Hospital.

  6. Assessment of the use of care for these hand dermatitis

    Time frame: Three months (at the end of study)

    Assessment of the use of care for these hand dermatitis

  7. atopic status

    Time frame: Three months (at the end of study)

    atopic status

  8. Percentage, means, and standard deviations of responses to quantitative and qualitative questions that appeal to the primary and secondary objectives.

    Time frame: Three months (at the end of study)

    Percentage, means, and standard deviations of responses to quantitative and

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Hand Dermatitis in the Care and Hospital Staff of the Brest CHRU: State of Play

Acronym: MANUS-PRO

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Oct 23, 2019
Registry last updated
Sep 11, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.