Occupational Hand Eczema - Testing of a Prevention-concept

Sponsor
National Allergy Research Center, Denmark (Other)
Overall Status
Recruiting
CT.gov ID
NCT04790799
Collaborator
Arbejdsmiljøforskningsfonden (Other), Bispebjerg Hospital (Other), Frederiksberg University Hospital (Other), National Research Centre for the Working Environment, Denmark (Other), University of Osnabrueck (Other)
250
1
2
30
8.3

Study Details

Study Description

Brief Summary

Randomised controlled trial examining the effect of decreased waiting time for the first doctors' appointment, patient education, glove counselling and counselling at departments of social or occupational medicine on severity of hand eczema, quality of life, use of corticosteroids, and jobsituation 3-12 months after intervention in patients with suspected occupational contact dermatitis of the hands.

Condition or Disease Intervention/Treatment Phase
  • Other: Treatment at the skin department at Gentofte Hospital
N/A

Detailed Description

Patients with suspected occupational hand eczema are recruited to the study on basis of their referral from general practitioner to dermatologist. Patients are randomised to either control or intervention group. The control group is treated and followed-up by the dermatologist they have been referred to, while the intervention group is treated and followed-up at Gentofte Hospital skin department with a maximum waiting time of 3 weeks. At the skin department at Gentofte Hospital, the patients in the intervention group receive patient education in prevention and treatment of hand eczema, glove counselling, personal product screening by a chemistry engineer, extended allergy testing and the standard treatment of hand eczema. Patients in both the control and intervention group are asked to fill out a questionnaire at 3, 6, 9 and 12 months after inclusion in the study. The questionnaire contains questions about quality of life, severity of hand exzema, jobsituation, use of healthcare service and use of medicine. Furthermore, prescriptions of medicine are registered in both control and intervention group at 3, 6, 9 and 12 months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
250 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Occupational Hand Eczema - Establishment and Testing of a Prevention-concept With Focus on the Young Workforce
Actual Study Start Date :
Jul 2, 2020
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Treatment in a hospital setting at Gentofte Hospital skin department with patient education, glove counselling, personal product screening by a chemistry engineer, extended allergy testing and the standard treatment of hand eczema.

Other: Treatment at the skin department at Gentofte Hospital
Treatment in a hospital setting at Gentofte Hospital skin department

No Intervention: Control group

Treatment as usual (at a dermatologist office).

Outcome Measures

Primary Outcome Measures

  1. Change in severity of handeczema assessed by the hand eczema severity index (HECSI) 0-360 points (0 best, 360 worst) [Change between baseline and 3 months]

    The hand eczema severity index (HECSI)

  2. Change in severity of handeczema assessed by the photographic guide for severity of handeczema [Change between baseline and 3 months]

    Self-assessed photographic guide

  3. Change in severity of handeczema assessed by the photographic guide for severity of handeczema [Change between baseline and 6 months]

    Self-assessed photographic guide

  4. Change in severity of handeczema assessed by the photographic guide for severity of handeczema [Change between baseline and 9 months]

    Self-assessed photographic guide

  5. Change in severity of handeczema assessed by the photographic guide for severity of handeczema [Change between baseline and 12 months]

    Self-assessed photographic guide

  6. Change in severity of handeczema assessed by a visual analog score 0-100 (0 best, 100 worst) [Change between baseline and 3 months]

    Visual analog Score for severity of handeczema

  7. Change in severity of handeczema assessed by a visual analog score 0-100 (0 best, 100 worst) [Change between baseline and 6 months]

    Visual analog Score for severity of handeczema

  8. Change in severity of handeczema assessed by a visual analog score 0-100 (0 best, 100 worst) [Change between baseline and 9 months]

    Visual analog Score for severity of handeczema

  9. Change in severity of handeczema assessed by a visual analog score 0-100 (0 best, 100 worst) [Change between baseline and 12 months]

    Visual analog Score for severity of handeczema

  10. Amount of corticosteroids prescribed within the last year [Baseline]

    Amount of corticosteroids prescribed wihtin the last year

  11. Amount of corticosteroids prescribed within the last 3 months [3 months]

    Amount of corticosteroids prescribed within the last 3 months

  12. Amount of corticosteroids prescribed within the last 3 months [6 months]

    Amount of corticosteroids prescribed within the last 3 months

  13. Amount of corticosteroids prescribed within the last 3 months [9 months]

    Amount of corticosteroids prescribed within the last 3 months

  14. Amount of corticosteroids prescribed within the last 3 months [12 months]

    Amount of corticosteroids prescribed within the last 3 months

  15. Health-Related Quality of Life assessed by Skindex-29, scale ranging from 0-100 points (higher score = higher impact of skin disease on quality of life) [Baseline]

    Skindex-29

  16. Health-Related Quality of Life assessed by Skindex-29, scale ranging from 0-100 points (higher score = higher impact of skin disease on quality of life) [3 months]

    Skindex-29

  17. Health-Related Quality of Life assessed by Skindex-29, scale ranging from 0-100 points (higher score = higher impact of skin disease on quality of life) [6 months]

    Skindex-29

  18. Health-Related Quality of Life assessed by Skindex-29, scale ranging from 0-100 points (higher score = higher impact of skin disease on quality of life) [9 months]

    Skindex-29

  19. Health-Related Quality of Life assessed by Skindex-29, scale ranging from 0-100 points (higher score = higher impact of skin disease on quality of life) [12 months]

    Skindex-29

  20. Health-Related Quality of Life assessed by "European Quality of Life - 5 Dimensions" (EQ-5D) [Baseline]

    "European Quality of Life - 5 Dimensions" (EQ-5D)

  21. Health-Related Quality of Life assessed by "European Quality of Life - 5 Dimensions" (EQ-5D) [3 months]

    "European Quality of Life - 5 Dimensions" (EQ-5D)

  22. Health-Related Quality of Life assessed by "European Quality of Life - 5 Dimensions" (EQ-5D) [6 months]

    "European Quality of Life - 5 Dimensions" (EQ-5D)

  23. Health-Related Quality of Life assessed by "European Quality of Life - 5 Dimensions" (EQ-5D) [9 months]

    "European Quality of Life - 5 Dimensions" (EQ-5D)

  24. Health-Related Quality of Life assessed by "European Quality of Life - 5 Dimensions" (EQ-5D) [12 months]

    "European Quality of Life - 5 Dimensions" (EQ-5D)

  25. Health-Related Quality of Life assessed by Dermatology life quality index (DLQI) 0-30 (higher score = higher impact of skin disease on quality of life) [Baseline]

    Dermatology life quality index (DLQI)

  26. Health-Related Quality of Life assessed by Dermatology life quality index (DLQI) 0-30 (higher score = higher impact of skin disease on quality of life) [3 months]

    Dermatology life quality index (DLQI)

  27. Health-Related Quality of Life assessed by Dermatology life quality index (DLQI) 0-30 (higher score = higher impact of skin disease on quality of life) [6 months]

    Dermatology life quality index (DLQI)

  28. Health-Related Quality of Life assessed by Dermatology life quality index (DLQI) 0-30 (higher score = higher impact of skin disease on quality of life) [9 months]

    Dermatology life quality index (DLQI)

  29. Health-Related Quality of Life assessed by Dermatology life quality index (DLQI) 0-30 (higher score = higher impact of skin disease on quality of life) [12 months]

    Dermatology life quality index (DLQI)

  30. Number of participants with loss of job within the last year [Baseline]

    Self-repported loss of job wihtin the last year

  31. Number of participants with loss of job within the last 3 months [Baseline]

    Self-repported loss of job within the last 3 months

  32. Number of participants with loss of job within the last 3 months [3 months]

    Self-repported loss of job within the last 3 months

  33. Number of participants with loss of job within the last 3 months [6 months]

    Self-repported loss of job within the last 3 months

  34. Number of participants with loss of job within the last 3 months [9 months]

    Self-repported loss of job within the last 3 months

  35. Number of participants with loss of job within the last 3 months [12 months]

    Self-repported loss of job within the last 3 months

  36. Amount of sick leave within the last year [Baseline]

    Self-repported amount of sick leave within the last year

  37. Amount of sick leave within the last 3 months [3 months]

    Self-repported amount of sick leave within the last 3 months

  38. Amount of sick leave within the last 3 months [6 months]

    Self-repported amount of sick leave within the last 3 months

  39. Amount of sick leave within the last 3 months [9 months]

    Self-repported amount of sick leave within the last 3 months

  40. Amount of sick leave within the last 3 months [12 months]

    Self-repported amount of sick leave within the last 3 months

  41. Number of participants with change of occupation due to occupational contact dermatitis within the last year [Baseline]

    Change of occupation due to occupational contact dermatitis within the last year

  42. Number of participants with change of occupation due to occupational contact dermatitis within the last 3 months [3 months]

    Change of occupation due to occupational contact dermatitis within the last 3 months

  43. Number of participants with change of occupation due to occupational contact dermatitis within the last 3 months [6 months]

    Change of occupation due to occupational contact dermatitis within the last 3 months

  44. Number of participants with change of occupation due to occupational contact dermatitis within the last 3 months [9 months]

    Change of occupation due to occupational contact dermatitis within the last 3 months

  45. Number of participants with change of occupation due to occupational contact dermatitis within the last 3 months [12 months]

    Change of occupation due to occupational contact dermatitis within the last 3 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Referred from a general practitioner to a dermatologist

  • Hand eczema within the last 3 months

  • Suspicion that the hand eczema is work-related (either patient and/or doctors suspicion)

Exclusion Criteria:
  • Does not read and write danish

  • Severe psychiatric illness

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gentofte Hospital, Skin department Hellerup Denmark 2900

Sponsors and Collaborators

  • National Allergy Research Center, Denmark
  • Arbejdsmiljøforskningsfonden
  • Bispebjerg Hospital
  • Frederiksberg University Hospital
  • National Research Centre for the Working Environment, Denmark
  • University of Osnabrueck

Investigators

  • Study Director: Jeanne D Johansen, Professor, National Allergy Research Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jojo Biel-Nielsen Dietz, Medical doctor, Ph.d.-student, National Allergy Research Center, Denmark
ClinicalTrials.gov Identifier:
NCT04790799
Other Study ID Numbers:
  • P-2019-650
First Posted:
Mar 10, 2021
Last Update Posted:
Mar 12, 2021
Last Verified:
Mar 1, 2021
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 12, 2021