Carmel Moore
Chelmsford, East of England, CM1 1SQ, United Kingdom
NCT Number: NCT04749966
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Chelmsford, East of England, CM1 1SQ, United Kingdom
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:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
This is an observational study, there are no interventions
Time frame: From the start to the end of recruitment at each participating site, approximately 4 weeks
The number of staff volunteering to take part
Time frame: From the start to the end of recruitment at each participating site, approximately 4 weeks
The proportion of staff estimated to have been targeted through study advertising who volunteer to take part
Time frame: From the start to the end of recruitment at each participating site, approximately 4 weeks
The proportion of staff volunteering to take part in the study who are eligible
Time frame: At Day 3 of the lifestyle assessment
The proportion of time the heart rate monitor was worn by participants measured using data collected by the monitor
Time frame: At Day 3 of the lifestyle assessment
The proportion of participants completing the journal
Time frame: On completion of interviews i.e. at approximately 8 weeks
The proportion of participants in whom an interview is arranged and completed
Time frame: Measured during lifestyle assessment over a period of 3 days - at approximately 3 weeks post-recruitment
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.
Time frame: On completion of interviews i.e. at approximately 8 weeks
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.
Anglia Ruskin University
Other
Understanding Wellbeing Among Emergency Service Staff by Mapping Physiological Indicators and Subjective Mediators of Stress: An Observational Feasibility Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07109050
Palliative Care, Virtual Reality
Lincoln, United Kingdom
View Trial DetailsNCT07364383
Microbiome, Probiotic
Sofia, Bulgaria
View Trial DetailsNCT06845059
Attitude, Behavior
Wroclaw, Lower Silesian Voivodeship, Poland
View Trial DetailsNCT07480018
Anaerobic Power, Behavior
Greeley, Colorado, United States
View Trial Details