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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02230774
Other study ID # 12118
Secondary ID
Status Completed
Phase N/A
First received July 14, 2014
Last updated September 2, 2014
Start date March 2013
Est. completion date July 2014

Study information

Verified date September 2014
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

The main purpose of this study is to assess and compare the hydration status of medical and nursing staff and to investigate the relationship between the hydration status, cognitive function and serum cortisol (marker of stress).

We hypothesise that a significant proportion of doctors and nurses will be dehydrated at the end of their working day. Some, as in other occupations, may be dehydrated at the start of their working day. This is likely to be associated with impairment in cognitive performance at the end of the working day compared to the beginning and expected to be more pronounced after a night shift. There may be less noticeable difference amongst nursing staff given the protected break time. Dehydration and associated impairment in cognition is of important clinical value as it can impact patient care. participants will be involved in the study for two shifts (one day and one night), aiming at 15 medical and 15 surgical nurses as well as 15 medical (total 15 day and 15 night shifts from each group) and surgical doctors (total 15 day and 15 night shifts from each group). Those that do not work both day and night shifts will participate for only one shift and a new participant will be recruited until target number of shifts is achieved.


Description:

End points

1. To assess the hydration status of hospital staff nurses and doctors oncall at work by measuring the following:

1. Urine and serum osmolality

2. Urine mass produced during the shift

3. Kidney function (U &Es)

4. Bioimpedance measures

2- To assess the effect of hydration on status of cognitive function and subjective feelings.

3- To assess the association between hydration status on stress hormone (cortisol) levels.

Inclusion criteria All medical and nursing staff working on acute medical and surgical admissions at the Queens Medical Centre Nottingham.

Exclusion Criteria:

Pregnancy Pre-existing kidney disease Patients on diuretics Unwell in the past 6 week with acute illness that warrants hospital admission or prescribed medication.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- All medical and nursing staff working on acute medical and surgical admissions at the Queens Medical Centre Nottingham

Exclusion Criteria:

- Pregnancy Pre-existing kidney disease Patients on diuretics Unwell in the past 6 week with acute illness that warrants hospital admission or prescribed medication.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Queens Medical Centre Nottingham Nottinghamshire

Sponsors (3)

Lead Sponsor Collaborator
University of Nottingham European Hydration Institute, Loughborough University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess the prevalence of dehydration in nurses and doctors oncall. Using urine osmolality as a marker of hydration we aim to assess the prevalence of dehydration in health care professionals before and after day and night shifts. Comparing nurses and doctors oncall, day and night as well diffrence between those working in medical and surgical admissions. Participants will be followed up for the duration of their shift, approximately 12- 14 hours. No
Secondary Impact of hydration status on cognitive function We aim to assess the impact of hydration on key executive cognitive before and after day and night shifts, comparing day and night using the following tests:
Visual search
Stroop
Sternberg
Corsi
Participants will be followed up for the duration of their shift, approximately 12- 14 hours. No
Secondary The impact of hydration status on serum cortisol concentrations The impact of hydration status on serum cortisol concentrations as a surrogate marker of stress will be assessed before and after day and night shifts. with day and night shifts assessed separately given the diurnal variations in cortisol. Participants will be followed up for the duration of their shift, approximately 12- 14 hours. No
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