Work Ability-Productivity Among Clinical Health Workers Endometriosis Study

NCT ID: NCT05770843

Last Updated: 2023-03-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-03-31

Study Completion Date

2023-11-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Endometriosis

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Birkbeck, University of London

OTHER

Sponsor Role lead

Responsible Party

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Krystle Thomas Vedat

Doctoral student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Birkbeck, University of London

London, , United Kingdom

Site Status

Countries

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United Kingdom

Facility Contacts

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Krystle Thomas Vedat

Role: primary

Other Identifiers

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50727

Identifier Type: -

Identifier Source: org_study_id

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