Skip to main content
Clinical Trials/NCT03133364
NCT03133364
Completed
Not Applicable

Developing and Testing Delicious and Nutritious for the Old People

University of Copenhagen1 site in 1 country52 target enrollmentStarted: May 17, 2017Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
1
Primary Endpoint
Health related quality of life (EQ-5D-3L)

Overview

Brief Summary

Meals-on wheels may play a major role in contributing to better nourishment and quality of life in older people, thus delaying costly hospitalisation. Still, dwelling, old adults who receive meals-on-wheels are a population at risk of undernutrition leading to a decreased quality of life.

Hypothesis Offering nutritious ELDORADO meals as meals-on-wheels to nursing home residents in 3 months is an effective way to increase quality of life.

Aim To improve quality of life and functional abilities in nursing home residents by offering nutritious ELDORADO meals.

Detailed Description

Intervention The intervention group (n=50) will receive an optimized menu (in both sensory and nutritious aspects) for 12 weeks. In cooperation with the Copenhagen house of food and sensory staff, 19 main meals and 12 between-meals have been optimized based on nursing home residents' evaluations of sensory aspects. On a daily basis the menu will consist of 1 optimized main meal and 1 optimized between-meal, served for dinner. There will be no selective choice for the elderly. If a participant does not want the daily meal, he will receive another meal from the ordinary menu from the kitchen.

Control In comparison, the control group (n=50) will receive the same menu as the intervention group, however, the meals are not optimized on sensory and nutritious aspects. On a daily basis this menu also includes 1 main meal and 1 between-meal in 12 weeks. If a participant does not want the daily meal, he will receive another meal from the ordinary menu from the kitchen.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Care Provider, Investigator)

Masking Description

Participants are randomized to the control group (C) and intervention group (I) using the programme "Research randomizer". The main supervisor will manage the randomization.

Participants are blinded to whether they receive the control or intervention menu. Each menu will daily consist of a main meal and a between-meal.

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Living at Skovhuset, nursing home in Hillerød municipality, Denmark.
  • Collecting the "energy-dense diet" "ældrekost" with 40 % fat, with a main meal and a dessert/starter.
  • Able to understand and follow instructions for the procedures of the study.
  • Above 65 years.

Exclusion Criteria

  • Have chewing or swallowing difficulties.
  • Have acute disease or acute change in chronic disease.
  • Living after special nutritional standards e.g. vegetarian, have any food allergies, or if a participant is excluding common foods from their diet because of other reasons.
  • Not able or willing to give informed consent.

Outcomes

Primary Outcomes

Health related quality of life (EQ-5D-3L)

Time Frame: 12 weeks

(EQ-5D-3L) is a standardized instrument for use as a measure of health outcome. The EQ-5D-3L descriptive system comprises the following 5 dimensions (5D): mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels (3L): no problems (1 point), some problems (2 points), extreme problems (3 points). This gives a total of 245 different health states, adding unconscious and dead.

Secondary Outcomes

  • MMSE (mini mental status)(12 weeks)
  • Height(12 weeks)
  • Chair stand(12 weeks)
  • EVS(12 weeks)
  • Liking(One month in the middle of the intervention)
  • Compliance(12 weeks)
  • Hand grip strenght(12 weeks)
  • Diet registration(4 days)
  • Satisfaction with food related life (SWFL)(12 weeks)
  • Observations of meals(One month in the middle of the intervention)
  • Weight(12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Arne Astrup

Head of institute (Nutrition Exercise and Sports)

University of Copenhagen

Study Sites (1)

Loading locations...

Similar Trials