Work ACHES: Work Ability-Productivity Among Clinical Health Workers Endometriosis Study

Sponsor
Birkbeck, University of London (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05770843
Collaborator
(none)
20
1
8
2.5

Study Details

Study Description

Brief Summary

A qualitative multicentre study protocol. The prospective research explores clinical health workers with a diagnosis of endometriosis, experiencing regular pain and their perceptions of work ability-productivity.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Endometriosis has a significant impact on women at work physically, psychologically, and socially. Notably, pain is the most common reported concern, and considerably reduces work ability and productivity. However, previous research has principally focused on general workers, discounting the varied nature of work roles. Health workers appear to have an increased occupational risk of developing the condition, when compared with other shift workers and the general working population. Taking these findings into account, the prospective WORK ACHES study explores the relationship between clinical health workers' regular endometriosis pain, and their perceptions of work ability-productivity during such events.

    This multicentre qualitative study will invite employees with a diagnosis of endometriosis and working in clinical settings, to participate in the study. Recruitment will be carried out through study posters displayed in staff areas and occupational health departments, as well as snowballing methods. Semi-structured interviews will take place via Microsoft Teams to discuss participants' experiences of endometriosis pain at work and their work ability-productivity while symptomatic. Thematic analysis will be performed to interpret the data.

    The study has sought ethical approval from Birkbeck University of London's ethics Committee, the Integrated Research Application System and the Health Research Authority. Following the completion of the study, a summary of findings will be shared with participants and agreed hospitals. The full study report will also be disseminated to all parties involved and accessed through the University of London's library thesis collection and published in relevant specialty journals.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    20 participants
    Observational Model:
    Other
    Time Perspective:
    Other
    Official Title:
    Work Ability-Productivity Among Clinical Health Workers Endometriosis Study (Work ACHES): Protocol
    Anticipated Study Start Date :
    Mar 1, 2023
    Anticipated Primary Completion Date :
    Oct 1, 2023
    Anticipated Study Completion Date :
    Nov 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Perception of work ability-productivity during endometriosis associated pain [Up to 45 minutes]

      Semi-structured interviews will be used to examine clinical health workers' perceived work ability-productivity during episodes of endometriosis associated pain.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Women aged between 18-65 years.

    • Employed working within a clinical setting health role.

    • English speaking.

    • Currently working full or part time hours.

    • Diagnosis of endometriosis (as reported by participant, as medical records will not be accessed for the purpose of this study).

    • Experiences regular endometriosis associated pain.

    Exclusion Criteria:
    • Painful comorbidities.

    • Unemployed women.

    • Pregnant women.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Birkbeck, University of London London United Kingdom

    Sponsors and Collaborators

    • Birkbeck, University of London

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Krystle Thomas Vedat, Doctoral student, Birkbeck, University of London
    ClinicalTrials.gov Identifier:
    NCT05770843
    Other Study ID Numbers:
    • 50727
    First Posted:
    Mar 16, 2023
    Last Update Posted:
    Mar 17, 2023
    Last Verified:
    Mar 1, 2023
    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 Krystle Thomas Vedat, Doctoral student, Birkbeck, University of London
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2023