Optimisation of Nutrition and Medication for Acutely Admitted Older Medical Patients

NCT03741283 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 193

Last updated 2021-08-25

No results posted yet for this study

Summary

Malnutrition and inappropriate medication prescribing are highly prevalent among acutely admitted older medical patients leading to re-admissions, frailty, poor physical, performance compromised quality of life and mortality. Thus, the aim of this study is to optimise the nutrition and medication in older medical patients admitted to an acute care department at admission and up to 16 weeks after discharge. Participants in the intervention group receives a medication review and participants with malnutrition or risk of malnutrition additionally receive a transitional multimodal intervention. The control group receives standard care.

Conditions

  • Aging
  • Malnutrition
  • Drug Prescribing

Interventions

OTHER

Optimisation of nutrition and medication

1. Inter-professional optimisation of medication prescribing: Study participants in the intervention group receives optimisation of medication prescribing at admission day (baseline) regardless of nutritional state. The intervention is performed in cooperation between a clinical pharmacist and a medical physician. 2. Nutritional intervention: If positive screening for malnutrition or risk of malnutrition a dietetic intervention is initiated and if positive screening below interventions are initiated: * Dysphagia: occupational therapy intervention. * Oral cavity problems: odontological intervention. * Depression: geriatric intervention. * Low ADL: occupational therapy intervention and if positive screening for poor muscle strength: physiotherapeutic intervention.

Sponsors & Collaborators

  • Clinical Research Centre

    collaborator UNKNOWN
  • Region Hovedstadens Apotek

    collaborator OTHER_GOV
  • Udviklings- og forskningspuljen, Danske Regioner og Sundhedskartellet

    collaborator UNKNOWN
  • Region Capital Denmark

    collaborator OTHER
  • Regionernes Lægemiddelorganisation

    collaborator UNKNOWN
  • Hvidovre University Hospital

    lead OTHER

Principal Investigators

  • Ove Andersen, MD, PhD · Hvidovre University Hospital

  • Aino L. Andersen, MSc · Hvidovre University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-15
Primary Completion
2022-07-15
Completion
2022-07-15

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03741283 on ClinicalTrials.gov