Validation of Two Acitivity Monitors in Three Inpatient Populations.

NCT ID: NCT04120740

Last Updated: 2019-11-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

36 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-10

Study Completion Date

2019-11-18

Brief Summary

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The aim of this study is to investigate the validity of Sens Motion and ActivPAL acitivity monitors. Thirthy-six patients from three different patient populations will be included: 12 acute high-risk abdominal surgery patients (+18 years), 12 hip fracture patients (+65) and 12 older medical patients (+65).

Each patient will be asked to wear two sets of activity monitors while performing a predefined researcher-supervised protocol consisting of a range of positions and activities including lying down, sitting, standing and walking.

Observations measured by time in each position will be used as a golden standard for physical activity and thus compared with the data produced by the acitivity monitors.

Detailed Description

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The study will investigate the association between activity measured by Sens Motion and ActivPAL acitivity monitors, respectively, and direct observation in order to investigate to which degree the two types of activity monitors are able to classify activity (i.e. lying, sitting, standing, walking, up/down transitions and steps).

Thirty-six patients from three different patient populations will be included: 12 acute high-risk abdominal surgery patients (+18 years), 12 hip fracture patients (+65) and 12 older medical patients (+65). Inclusion criteria to be fullfilled: 1) admission from own home. Patients will be excluded for the following reasons: inability to walk independently with or without a walking aid; inability to transfer from lying to sitting, inability to transfer from sitting to standing, inability to cooperate, and inability to speak or understand Danish.

Each patient will be asked to wear two sets of activity monitors (on the right thigh and on the chest) while performing a predefined, supervised protocol consisting of a range of positions and activities including lying down, sitting, standing and walking.

Conditions

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Hip Fractures Abdominal Surgery Medical Patients

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* older medical patient (+65)
* older hip fracture patient (+65)
* acute high-risk abdominal surgery patient (+18)
* admitted from own home

Exclusion Criteria

* inability to walk independently with or without a walking aid
* inability to transfer from lying to sitting and sitting to standing
* inability to cooperate
* inability to understand or speak Danish.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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SENS Innovation Aps

UNKNOWN

Sponsor Role collaborator

Mette Merete Pedersen

OTHER

Sponsor Role lead

Responsible Party

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Mette Merete Pedersen

Postdoctoral fellow

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Mette M Pedersen, Postdoc

Role: STUDY_CHAIR

Hvidovre University Hospital

Locations

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Copenhagen University Hospital, Hvidovre

Hvidovre, , Denmark

Site Status

Countries

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Denmark

References

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Pedersen BS, Kristensen MT, Josefsen CO, Lykkegaard KL, Jonsson LR, Pedersen MM. Validation of Two Activity Monitors in Slow and Fast Walking Hospitalized Patients. Rehabil Res Pract. 2022 May 16;2022:9230081. doi: 10.1155/2022/9230081. eCollection 2022.

Reference Type DERIVED
PMID: 35615755 (View on PubMed)

Other Identifiers

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HH-SENS-FYS-01

Identifier Type: -

Identifier Source: org_study_id

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