Blue Light Emergency Services Wellbeing Feasibility Study

Wellbeing Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04749966
• Other study ID #: 19_20_029
• Secondary ID: IRAS 278059
• Status: Completed
• Start date: February 15, 2021
• Est. completion date: October 27, 2021

Study information

• Verified date: October 2021
• Source: Anglia Ruskin University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: October 27, 2021
• Est. primary completion date: October 27, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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).

Exclusion Criteria:

• off-duty or on leave during the study period

• part-time (or on-call) employees

• not working shift patterns

• currently taking part in research that may impact on results, design or scientific value of this study (or other studies)

• not able to read or understand the English Language as it will not be possible to provide translation services for the study

In addition, the results from the heart rate monitor may be unreliable with certain medical conditions and, as such, staff will not be able to take part if they have had a heart transplant or if they have a pacemaker, heart disease, atrial fibrillation, atrial flutter or uncontrolled thyroid disorder.

Related Conditions & MeSH terms

• Emergencies
• Wellbeing

Intervention

Other:
• This is an observational study, there are no interventions
This is an observational study, there are no interventions

Locations

Country	Name	City	State
United Kingdom	Carmel Moore	Chelmsford	East Of England

Sponsors (1)

Lead Sponsor	Collaborator
Anglia Ruskin University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of study recruitment - the number of staff volunteering to take part	The number of staff volunteering to take part	From the start to the end of recruitment at each participating site, approximately 4 weeks
Primary	Feasibility of study recruitment - the proportion of staff targeted through study advertising who volunteer to take part	The proportion of staff estimated to have been targeted through study advertising who volunteer to take part	From the start to the end of recruitment at each participating site, approximately 4 weeks
Primary	Feasibility of study recruitment - the proportion of staff volunteering to take part in the study who are eligible	The proportion of staff volunteering to take part in the study who are eligible	From the start to the end of recruitment at each participating site, approximately 4 weeks
Primary	Adherence to heart rate monitoring during 3-day lifestyle assessment	The proportion of time the heart rate monitor was worn by participants measured using data collected by the monitor	At Day 3 of the lifestyle assessment
Primary	Adherence to completion of online journal during 3-day lifestyle assessment	The proportion of participants completing the journal	At Day 3 of the lifestyle assessment
Primary	Feasibility of conducting interviews	The proportion of participants in whom an interview is arranged and completed	On completion of interviews i.e. at approximately 8 weeks
Secondary	Heart rate variance	Heart 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.	Measured during lifestyle assessment over a period of 3 days - at approximately 3 weeks post-recruitment
Secondary	Subjective mediators of stress	Subjective 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.	On completion of interviews i.e. at approximately 8 weeks