Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
48 participants
OBSERVATIONAL
2015-09-22
2016-08-03
Brief Summary
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Before designing a food intervention study, there is a need to, firstly:
1. describe hospital food intake, eating habits and preferences in elderly inpatients during hospitalization
2. describe predictors of hospital food intake in elderly during hospitalisation
3. compare energy and protein intake in elderly inpatients during hospitalisation with the United Kingdom Dietary Reference Values (DRVs)
This study is a hospital based observational study. Eligible participants will be 125 patients (aged ≥ 65 years old) admitted to the geriatric wards of 2 hospitals in the West of Scotland. Eligible participants will be seen 96 hours after admission in order to explain the study process and to obtain written consent. The researcher will record basic body size measurements and will ask the patient questions about living conditions, feelings, memory, health, eating habits, opinions about the hospital food service. Nursing staff will be asked about patient's functional activity. The researcher will also take pictures of a subset of patients' main meals (breakfast, lunch and dinner) on a single day, prior to and after eating. The researcher will meet each patient three times in total. The first time 4 days after admission; a second time, during the hospital stay and, finally, around the time of discharge to repeat some measurements including weight, BMI, skinfold, mid upper arm circumference, grip strength and calf circumference.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Study cohort
Patients aged 65 years or over admitted to a geriatric ward in 2 hospitals for more than 3 days
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Duration of hospital admission expected to be more than 3 days
* Able to provide consent or consent obtainable from their legal representative
Exclusion Criteria
65 Years
ALL
No
Sponsors
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University of Glasgow
OTHER
NHS Greater Glasgow and Clyde
OTHER
Responsible Party
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Principal Investigators
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Konstantinos Gerasimidis, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Glasgow
Other Identifiers
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GN15HN293
Identifier Type: -
Identifier Source: org_study_id
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