Clinical Trials Directory

Trials / Completed

CompletedNCT04749966

Blue Light Emergency Services Wellbeing Feasibility Study

Understanding Wellbeing Among Emergency Service Staff by Mapping Physiological Indicators and Subjective Mediators of Stress: An Observational Feasibility Study

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Anglia Ruskin University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Emergency Service teams operate in some of the most challenging workplaces and experience higher rates of mental ill health than the general population. Effective interventions are required to enhance wellbeing, but as a first step it is crucial to understand the context through which to develop these initiatives. This preliminary study will test the feasibility of implementing a larger study to map the relationship between physical responses associated with levels of stress (heart rate variability) and personal, social and organisational factors that mediate these responses. In doing so, it is hoped to provide an insight into factors that shape emergency staff members' response to stress to help develop and personalise wellbeing initiatives.

Detailed description

The study team is proposing a large study in the Essex Emergency Services to map the relationship between physiological indicators of stress and subjective mediators and, in doing, provide insight into factors that shape a staff members' response to stress, which could help to develop and personalise wellbeing initiatives. However, before undertaking a large study it is proposed to establish operational feasibility. This feasibility study will enrol ten shift-working staff from each of three emergency services (Essex Police, Essex County Fire and Rescue Service and East of England Ambulance Service Trust). Over a 3-day period, we will evaluate participants' physiological response to stressors by measuring HRV (using Firstbeat Bodyguard 2 beat-to-beat heart rate monitor). During the same period, participants will keep a personal online journal of events during the day. As part of the lifestyle assessment, data from the heart rate monitor and journal will be analysed and participants will receive a Summary Report including information on their body's reaction to stress and how this may be managed. Following the lifestyle assessment, the research team will facilitate semi-structured interviews; they will use participants' lifestyle assessment Summary Reports to inform appropriate questions. The team will discuss subjective experiences with participants as well as their overall experience with the data collection process. The objectives of the feasibility study are to: 1. Evaluate feasibility of undertaking a larger definitive study in terms of: * Willingness and eligibility of emergency services' staff to take part in the study * Recruitment timeframe * Participant adherence to lifestyle assessment protocols (including wearing a heart rate monitor and completing an online journal over a 3-day period) * Proportion of participants in whom an interview is arranged and completed * Feasibility of other operational aspects not included above. 2. Undertake an initial evaluation of physiological indicators and subjective mediators of stress and identify any i) associations between them and ii) patterns that emerge between individual participants.

Conditions

Interventions

TypeNameDescription
OTHERThis is an observational study, there are no interventionsThis is an observational study, there are no interventions

Timeline

Start date
2021-02-15
Primary completion
2021-10-27
Completion
2021-10-27
First posted
2021-02-11
Last updated
2022-02-09

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT04749966. Inclusion in this directory is not an endorsement.