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Clinical Trials/NCT01851928
NCT01851928
Completed
Not Applicable

The Validation of Two Inpatient Adult Nutrition Screening Tools in Cancer Care - a Prospective Study

Royal Marsden NHS Foundation Trust1 site in 1 country128 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adenocarcinoma of the Gastroesophageal Junction
Sponsor
Royal Marsden NHS Foundation Trust
Enrollment
128
Locations
1
Primary Endpoint
Sensitivity of Screening Tool
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The objective of this study is to evaluate the sensitivity and specificity of two nutrition screening tools to identify inpatients with malnutrition or at risk of malnutrition. The two tools are the Royal Marsden Abridged Adult Nutrition Screening Tool (AANST) and the Malnutrition Screening Tool (MST)[10] The tools will be compared with the currently accepted gold standard, Patient Generated Subjective Global Assessment (PG-SGA). Both screening tools are in the form of scored questionnaires and are suitable for electronic input.

The ultimate objective is to select an adult inpatient nutrition screening tool with the highest sensitivity for future use in the oncology inpatient setting in order to allow prompt commencement of an appropriate nutrition care plan.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
March 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All adult inpatients, over the age of 18, admitted to RMH for whom a measured weight and height can be obtained
  • Exclusion Criteria
  • Patients for whom it is not possible to obtain a measured height and weight
  • People with a definitive diagnosis of dementia
  • People who lack capacity to understand the purpose of the study and to consent
  • Patients who are unable to understand and speak English

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Sensitivity of Screening Tool

Time Frame: 24 hrs

The primary endpoint of the study is the sensitivity of each screening tool as compared to the gold standard of PG-SGA when completed by a trained dietitian.

Secondary Outcomes

  • Specificity of the Tool(24 hrs)

Study Sites (1)

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