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Intrinsic Capacity and Functional Ability Monitoring With an Integrated Data Eco-System for Healthy Ageing.

NCT06270979 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2024-02-21

No results posted yet for this study

Summary

In this study, 120 older adults (aged 65 years or older) either patients undergoing rehabilitation or older nursing home residents will be provided with an Eforto® device and the eco-System for Healthy Ageing (ISHA) mobile application to self-monitor intrinsic capacity for 4 months (if needed with assistance by an (in)formal caregiver). Preferably, the participants will use their own smartphone because mitigating smartphone-use-related issues.

The aims of the study are:

1. to evaluate the usability and feasibility of self-monitoring intrinsic capacity by using the ISHA system in rehabilitation and nursing home settings.
2. to investigate if changes and variability in intrinsic capacity as measured with ISHA are related to changes in functional ability and quality of life.
3. to explore individual trajectories of intrinsic capacity with the ISHA system.

Conditions

Interventions

DEVICE

ISHA

Participants will be provided with an Eforto® device and ISHA mobile application to self-monitor intrinsic capacity for 4 months (if needed with assistance by an (in)formal caregiver).

Sponsors & Collaborators

  • Leiehome vzw

    collaborator UNKNOWN

  • University Hospital, Antwerp

    collaborator OTHER

  • Universiteit Antwerpen

    collaborator OTHER

  • INNOVIRIS

    collaborator UNKNOWN

  • AAL

    collaborator UNKNOWN

  • Prof. Ivan Bautmans

    lead OTHER

Principal Investigators

  • Ivan Bautmans, Prof. Dr. · VUB

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-04-01
Primary Completion
2025-04-01
Completion
2025-04-01

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Entities

Diseases

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 NCT06270979 on ClinicalTrials.gov