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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01627496
Other study ID # NSQLOP
Secondary ID
Status Completed
Phase N/A
First received June 15, 2012
Last updated July 3, 2012
Start date September 2010
Est. completion date December 2011

Study information

Verified date July 2012
Source University of Surrey
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics CommitteeUnited Kingdom: National Health Service
Study type Observational

Clinical Trial Summary

The aim of this study is to determine the nutritional status, and factors affecting malnutrition in older people staying in hospitals.

Objectives:

- To recruit a sample of older people in hospital

- To collect information on nutritional status, satisfaction with food-related life and experience with access to food in hospital.

- To assess the staffing attitudes to nutritional care of the older adult

- To undertake an audit of therapeutic ('special') diets served in hospitals, with respect to their nutritional adequacy and wastage

- To investigate predictors and correlates of malnutrition within the hospital setting and compare these relationships with those previously identified in care homes and the community.

- To make recommendations for practice to improve the nutritional status of hospitalised older adults.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2011
Est. primary completion date January 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 75 Years and older
Eligibility Inclusion Criteria:

- Aged = 75 years old

- Male or female

- Duration of stay is more than 24hrs

- Able to eat normally

- Able to read and write English

- Able to be weighed standing or sitting OR accurate weight available since admission

Exclusion Criteria:

- Age below 75 years old

- Newly admitted patient (less than 24hrs)

- Certain medical conditions likely to affect digestion/ absorption of nutrients (researchers will assess)

- Unable to provide informed written consent

- Patients on gastric surgical wards or suffering from gastritis

- Patients currently taking laxatives

- Unable to be weighed and no measured weight available (self report weight is not adequate)

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Royal Surrey County Hospital Guildford Surrey

Sponsors (1)

Lead Sponsor Collaborator
University of Surrey

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nutritional status Using MNA baseline No
Primary Satisfaction with food related quality of life baseline No
Primary Dietary intake 3 x 24hr recalls baseline No
Secondary Food Access in Hospital baseline No
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