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FoodnGo-Empower: A Feasibility Study of Physical Activities and Nutrition of Older Patients by the Use of Technology

FoodnGo - Empower: A Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02703441
Enrollment
38
Registered
2016-03-09
Start date
2015-05-31
Completion date
2016-07-31
Last updated
2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malnutrition, Physical Activity

Brief summary

The research and innovation programme Food´n´Go - Empower aims to develop, test and implement health technology solutions for active involvement and increased empowerment of elderly patients and their relatives solving well-known problem areas as malnutrition and inactivity. The prototype was developed in 2013. The project is a collaboration between departement of internal medicine in Copenhagen University Hospital, one local municipality and a private it-company. The technology is a tablet computer, used by elderly patients to order and register food intake during hospitalization. The tablet is also used to get inspiration for physical activities during hospital admission and after discharge and for registration of physical activities. The aim of this study is to test if an adjusted version of the Food´n´Go technology through active involvement of the elderly patient can prevent weightloss and loss of muscle strength during hospitalization and after discharge.

Detailed description

Welfare and health technology are often directed at solving problems and meeting the needs of societies' most vulnerable groups often not familiar with computers. The research and innovation programme Food´n´Go - Empower aims to develop, test and implement health technology solutions for involvement and increased empowerment of elderly patients and their relatives. The focus is on frequent issues for this group of patients, in this phase focusing on nutrition and physical activity. Later, the solution will include pain management, management of sleep problems, medication management, prevention of confusion and coordination of the treatment and care course across sectorial borders. The technology is a tablet- computer, operated by the patient by means of a number of app-like software applications. In the summer 2013 the programme received a grant from the Capitol Region's Public-Private-Innovation (OPI) pool for design and development of the prototype. In 2014 the prototype for nutrition was tested in a feasibility study. Usability and acceptability was tested in the patients' own home, as well as the effect of the nutrition intervention, after discharge from hospital (see protocol 10/16/2014). The results were promising, and the aim is now to test the technology for supporting both nutrition and physical activity across sectorial boundaries. The elderly patient will operate the tablet during admission and after discharge, continuing the efforts aimed at nutrition and physical activity during the stay at a rehabilitation centre 5 to 6 weeks after discharge. The working hypothesis is: Functional ability and nutritional status will be stabilized or improved, and readmissions and dependency of municipal services will be reduced. The aim of this study is: 1. to test if an adjusted version of the Food´n´Go technology through active involvement of the elderly patient can prevent weight loss and loss of muscle strength during hospitalization and after discharge 2. to develop and test the technology in relation to stability, applicability and acceptability

Interventions

Patients randomized to the intervention group will receive a tablet computer with an app-like software solution supporting nutrition and physical activity. The patients operate the computer and order their meals from the hospital menu; register dietary intake, and receive feedback informing about their current status for protein and energy intake. Likewise, the patients use small series of brief videos instructing in daily life activities for strengthening their muscles. After this, they register their performed activities and will receive informing and motivating feedback. Nudging and prompting is part of the solution.

Sponsors

Tachista
CollaboratorUNKNOWN
Herlev Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ≥ 65 years old admitted to Department of Internal Medicine * Planned to be discharged to a temporary stay at the municipality training centre * Body Mass Index ≤ 20 * Patient experienced problems with solving daily physical activities * Minimal Mental State Examination (MMSE) ≥24 * Able to operate the computer * Able to collaborate in the physical activities * Has a relative who is willing to be supportive

Exclusion criteria

* Terminal patients * Patients who are not able to communicate or do not understand danish

Design outcomes

Primary

MeasureTime frameDescription
Change in lean body-massBaseline, 6 weeks and 12 weeksDEXA scanning,

Secondary

MeasureTime frameDescription
Change in weightbaseline, 6 and 12 weeks
Change in BMIbaseline, 6 and 12 weeks
Change in Health related Quality of Lifebaseline, 6 and 12 weeksEQ5D (European Quality 5Dimensions Scale)
Change in signs of depressionBaseline, 6 and 12 weeksGeriatric Depression Scale 5 (GDS5)
Number of days to first readmission24 weeksDanish National Patient Register
Mortality24 weeksDanish National Patient Register
Change in muscle strengthbaseline, 6 and 12 weekshandgrip strength

Other

MeasureTime frameDescription
Physical activity12 weeksRegistered by the patient at the computer
Dietary intake12 weeksRegistered by the patient at the computer
Technology functionality12 weeksResearch assistant observes and registers problems
Technology acceptability12 weeksQualitative interviews with patients and relatives
Technology stability12 weeksResearch assistant observes and registers problems

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026