NCT04865627

Brief Summary

The focus of this study will be to determine the accuracy of the MOX, the Axivity and Fitbit, Empatica and Chill+ activity monitors (with both custom-made and available algorithms) for the classification of lying, sitting, standing, walking and climbing stairs in hospitalized older people in Acute Care for the elderly (ACE) and geriatric rehabilitation units. In addition, the feasibility of the use of the activity monitors as a measurement tool in daily practice during hospitalization in the geriatric department will be investigated.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 22, 2021

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 21, 2021

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 29, 2021

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2022

Completed
Last Updated

July 30, 2025

Status Verified

July 1, 2025

Enrollment Period

1.1 years

First QC Date

April 21, 2021

Last Update Submit

July 25, 2025

Conditions

Keywords

geriatric inhospital rehabilitationelderlyactivity monitors

Outcome Measures

Primary Outcomes (1)

  • accuracy of the activity monitors compared to the observation

    accuracy of the activity monitors during the observation moment, second by second

    30 minutes

Secondary Outcomes (1)

  • usability of an activity monitor in daily practice on the ward

    one week

Study Arms (2)

independent walking with walking aid

the participant is able to walk with a walking aid and does not need further assistance.

Device: activity monitor

dependent walking with walking aid

the participant is able to walk with assistance and a walking aid

Device: activity monitor

Interventions

Both groups will wear three different activity monitors for one week. There is one observation moment which consists of four minutes lying, sitting, standing, walking and taking stairs. Participants will be filmed during this moment.

Also known as: accelerometer, activity sensor
dependent walking with walking aidindependent walking with walking aid

Eligibility Criteria

Age70 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodProbability Sample
Study Population

Participant are admitted to a geriatric ward in UZ Leuven, Belgium and use a walkingaid.

You may qualify if:

  • admitted to the rehabilitation or acute ward of UZ Leuven
  • walking with the use of a walkingaid
  • a signed informed consent form
  • an expected stay of at least 7 days

You may not qualify if:

  • medically unstable

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universitaire Ziekenhuizen Leuven

Leuven, 3000, Belgium

Location

Related Publications (1)

  • van Dijk M, Bijnens W, Van Driessche C, Van Meerbeek T, Allegaert P, Van Cleynenbreugel H, Verschueren S, Verheyden G, Tournoy J, Flamaing J. Accuracy of an Activity Monitor in Assessing Physical Activity of Hospitalized Geriatric Rehabilitation Patients With Slow Walking Speed Using a Walking Aid. J Aging Phys Act. 2024 Nov 20;33(3):243-250. doi: 10.1123/japa.2023-0319. Print 2025 Jun 1.

MeSH Terms

Conditions

Hip FracturesStrokeAbdominal Injuries

Interventions

Fitness Trackers

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg InjuriesCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Diagnostic EquipmentEquipment and SuppliesWearable Electronic DevicesElectrical Equipment and Supplies

Study Officials

  • Johan Flamaing, MD, PhD

    UZ Leuven, KU Leuven

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist

Study Record Dates

First Submitted

April 21, 2021

First Posted

April 29, 2021

Study Start

March 22, 2021

Primary Completion

May 1, 2022

Study Completion

May 1, 2022

Last Updated

July 30, 2025

Record last verified: 2025-07

Locations