Dehydration Clinical Trial
— HANDsOnOfficial title:
Hydration Amongst Nurses and Doctors Oncall
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 |
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.
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. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United Kingdom | Queens Medical Centre | Nottingham | Nottinghamshire |
Lead Sponsor | Collaborator |
---|---|
University of Nottingham | European Hydration Institute, Loughborough University |
United Kingdom,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT04079543 -
NPO and Patient Satisfaction in the Cath Lab
|
N/A | |
Recruiting |
NCT06063655 -
Effects of Two Novel Hydration Beverage Formulas on Rehydration in Adults
|
N/A | |
Completed |
NCT05111392 -
Hydration Dynamics and Influence of Beverage Composition
|
Phase 1/Phase 2 | |
Terminated |
NCT02486224 -
Metabolomic Analysis of the Impacts of Hydration Status on Exercise Performance
|
N/A | |
Recruiting |
NCT02249845 -
Comparing the Diagnostic Accuracy of Clinical Dehydration Scales Among Small Children
|
N/A | |
Completed |
NCT01285713 -
IV Glucose for Dehydration Treatment
|
Phase 2 | |
Withdrawn |
NCT00691275 -
Efficacy Study of IV Fluids Only vs Ondansetron to Treat Dehydration
|
N/A | |
Completed |
NCT00360204 -
Improving Health Outcomes for New Mothers and Babies
|
Phase 3 | |
Completed |
NCT00370968 -
Zinc-ORS in Severe and Complicated Acute Diarrhea
|
Phase 2/Phase 3 | |
Completed |
NCT04076995 -
INDIGO-2: The Effect of High Water Intake on Glucose Regulation in Low-drinkers
|
N/A | |
Recruiting |
NCT05768789 -
Buoy Electrolyte Study on Hydration Status of Active Men and Women
|
N/A | |
Not yet recruiting |
NCT05428228 -
Clinical Study to Evaluate the Effects of Two Novel Hydration Beverage Formulas on Rehydration in Healthy Adults
|
N/A | |
Completed |
NCT04997031 -
Tap Water Intake and Perceptions in US Latinx Adults
|
||
Completed |
NCT04536324 -
The Absorption Rate of Subcutaneous Infused Fluid
|
||
Completed |
NCT02926989 -
Intravenous Fluids in Hospitalised Children
|
Phase 4 | |
Completed |
NCT04874584 -
Culturally Tailored Nurse Coaching Study for Cancer Symptom Management
|
N/A | |
Completed |
NCT02265575 -
Hylenex-Assisted Resuscitation in Kenya (HARK) Trial for the Management of Dehydration
|
Phase 2 | |
Completed |
NCT02206581 -
Using Hydration Monitor to Detect Changes in the Hydration Status Athletes
|
N/A | |
Completed |
NCT01893853 -
Fluid Balance During Exercise in the Heat With Water, Flavored Placebo, or a Carbohydrate-electrolyte Beverage Intake (The APEX Study)
|
N/A | |
Completed |
NCT01503996 -
Drinking Habits of Glaucoma Patients and Age Matched Controls
|
N/A |