Feasibility of Nutritional Telemonitoring in Elderly Home Care Patients

NCT03211845 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-07-07

No results posted yet for this study

Summary

An optimal nutritional status is essential for healthy ageing. Telemonitoring might contribute to maintaining or improving nutritional status in elderly people.The objectives of this pilot study are to test the feasibility, acceptability and implementation fidelity of telemonitoring of nutritional parameters in community-dwelling older adults; to test the study procedures for effect evaluation; and to determine the likelihood of achieving desired impact on the primary and secondary outcomes.

Conditions

  • Undernutrition
  • Aging

Interventions

OTHER

Nutritional telemonitoring

Participants receive a weighing scale, pedometer and television channel in order to perform self-measurements and receive guidance on nutrition and physical activity. Nurses use a website in order to receive telemonitoring measurements and decide about proper follow-up. In case of risk of undernutrition, nurses provide personal advice to optimize nutritional status of the participant.

Sponsors & Collaborators

  • European Union

    collaborator OTHER
  • Consorci Sanitari de Terrassa

    collaborator OTHER
  • Viveris Technologies SA

    collaborator UNKNOWN
  • STMicroelectronics Grenoble 2 SAS

    collaborator UNKNOWN
  • Sirlan Technologies SAS

    collaborator UNKNOWN
  • Habitat Health Environment

    collaborator OTHER
  • Universite Paris 13

    collaborator UNKNOWN
  • Meditecnologia SA

    collaborator UNKNOWN
  • Cybermoor Ltd

    collaborator OTHER
  • Telecom Sante

    collaborator UNKNOWN
  • Zorggroep Noordwest-Veluwe

    collaborator OTHER
  • Wageningen University

    lead OTHER

Principal Investigators

  • Lisette de Groot, Professor · Wageningen University and Research

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-27
Primary Completion
2015-11-20
Completion
2015-11-20

Countries

  • Netherlands

Study Locations

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Entities

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 NCT03211845 on ClinicalTrials.gov