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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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04749966
Enrollment
30
Registered
2021-02-11
Start date
2021-02-15
Completion date
2021-10-27
Last updated
2022-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wellbeing

Keywords

Emergency services, wellbeing, stress, physiological responses, subjective mediators

Brief 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.

Interventions

OTHERThis is an observational study, there are no interventions

This is an observational study, there are no interventions

Sponsors

Anglia Ruskin University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* are aged 18 or older * full-time employees * work shift patterns and will be on-duty during the study period * are able to take part in and contribute to the study (see

Exclusion criteria

below).

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of conducting interviewsOn completion of interviews i.e. at approximately 8 weeksThe proportion of participants in whom an interview is arranged and completed
Adherence to heart rate monitoring during 3-day lifestyle assessmentAt Day 3 of the lifestyle assessmentThe proportion of time the heart rate monitor was worn by participants measured using data collected by the monitor
Adherence to completion of online journal during 3-day lifestyle assessmentAt Day 3 of the lifestyle assessmentThe proportion of participants completing the journal
Feasibility of study recruitment - the number of staff volunteering to take partFrom the start to the end of recruitment at each participating site, approximately 4 weeksThe number of staff volunteering to take part
Feasibility of study recruitment - the proportion of staff targeted through study advertising who volunteer to take partFrom the start to the end of recruitment at each participating site, approximately 4 weeksThe proportion of staff estimated to have been targeted through study advertising who volunteer to take part
Feasibility of study recruitment - the proportion of staff volunteering to take part in the study who are eligibleFrom the start to the end of recruitment at each participating site, approximately 4 weeksThe proportion of staff volunteering to take part in the study who are eligible

Secondary

MeasureTime frameDescription
Subjective mediators of stressOn completion of interviews i.e. at approximately 8 weeksSubjective mediators include personal, social and organisational factors identified through semi-structured interviews. Qualitative thematic analysis techniques will be used to identify individual and group characteristics and subjective mediators associated with periods of stress.
Heart rate varianceMeasured during lifestyle assessment over a period of 3 days - at approximately 3 weeks post-recruitmentHeart rate variance will be measured as a physiological indicator of stress via a heart rate monitoring device worn by each participant over a 3-day period.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026