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Hydration and Outcome in Older Patients (HOOP)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01703715
First Posted: October 10, 2012
Last Update Posted: July 15, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Nottingham
  Purpose

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 Intervention
Dehydration Device: The Hydrant

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Hydration and Outcome in Older Patients

Resource links provided by NLM:


Further study details as provided by University of Nottingham:

Primary Outcome Measures:
  • Serum Osmolality [ Time Frame: At admission and 48hrs post admission to hospital ]

Biospecimen Retention:   Samples With DNA
Participants provide 5mls of whole blood on admission, at 48 hours post admission and at 3 month following discharge. This blood is to be analysed for urea, creatinine, sodium, potassium, osmolality, full blood count as well as renin and aldosterone.

Enrollment: 200
Study Start Date: August 2012
Study Completion Date: May 2014
Primary Completion Date: April 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
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.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   65 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
All patients admitted acutely to medical wards who are aged 65 years and over.
Criteria

Inclusion Criteria:

  1. - All patients of 65 years and over that are admitted acutely to medical wards
  2. - Ward staff who have been working in the clinical area for the duration of the trial (The Hydrant part of the study).

Exclusion Criteria:

  1. - Patients who are moribund
  2. - Patients who are doubly incontinent
  3. - Patients on the end of life pathway
  4. - Patients with terminal illness with a known life expectancy less than 3 months
  Contacts and Locations
Information from the National Library of Medicine

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


Locations
United Kingdom
Queens Medical Centre
Nottingham, Nottinghamshire, United Kingdom, NG7 2UH
Sponsors and Collaborators
University of Nottingham
Investigators
Principal Investigator: Dileep N Lobo, MD, FRCS University of Nottingham
  More Information

Responsible Party: University of Nottingham
ClinicalTrials.gov Identifier: NCT01703715     History of Changes
Other Study ID Numbers: 12029
First Submitted: October 5, 2012
First Posted: October 10, 2012
Last Update Posted: July 15, 2014
Last Verified: July 2014

Keywords provided by University of Nottingham:
Hydration
Elderly patients
Age 65 years and over
Admitted acutely to medical admissions ward

Additional relevant MeSH terms:
Dehydration
Water-Electrolyte Imbalance
Metabolic Diseases
Pathologic Processes