Hydration and Outcome in Older Patients (HOOP)
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|ClinicalTrials.gov Identifier: NCT01703715|
Recruitment Status : Completed
First Posted : October 10, 2012
Last Update Posted : July 15, 2014
Dehydration is recognised as a major issue in healthcare. Recovery after illness, extended length of stay, pressure sores and slow tissue recovery can all be impacted by dehydration. One of the biggest problems for many people with regard to getting a drink is easy, independent access - if they can't reach the jug/cup without a struggle then they often will go thirsty and potentially become dehydrated.
The purpose of this study is to investigate the impact of dehydration on outcome in patients 65 years and over. Furthermore we aim to assess the impact of providing easy, 24 hour, independently accessible fluids on reducing dehydration as well as improving patient experience.
We hypothesise that patients who are dehydration will take longer to recover from illness and stay in hospital for longer periods.
|Condition or disease||Intervention/treatment|
|Dehydration||Device: The Hydrant|
|Study Type :||Observational|
|Actual Enrollment :||200 participants|
|Official Title:||Hydration and Outcome in Older Patients|
|Study Start Date :||August 2012|
|Primary Completion Date :||April 2014|
|Study Completion Date :||May 2014|
Patients aged 65 years and over
All patients aged 65 years and over admitted to acutely to medical wards
Device: The Hydrant
The Hydrant is a new form of "drinking system" that may be used to provide continuous access to hydration will be given to 20 patients. 10 of the patients will have mild cognitive impairment with Mini Mental State Examination less than 24 and 10 with normal cognitive function. Patients and staff will be interviewed to assess the feasibility of the hydrant.
- Serum Osmolality [ Time Frame: At admission and 48hrs post admission to hospital ]
Biospecimen Retention: Samples With DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01703715
|Queens Medical Centre|
|Nottingham, Nottinghamshire, United Kingdom, NG7 2UH|
|Principal Investigator:||Dileep N Lobo, MD, FRCS||University of Nottingham|