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Contribution of Actigraphy for the Evaluation of Elbow Range of Motion in the Joint Assessment in Gerontology

Contribution of Actigraphy for the Evaluation of Elbow Range of Motion in the Joint Assessment in Gerontology

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01462760
Acronym
BIOVAL
Enrollment
85
Registered
2011-10-31
Start date
2011-10-31
Completion date
2012-08-31
Last updated
2011-10-31

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

Conditions

Geriatric Disorder

Brief summary

In this study, the investigators will measure range of motion of the elbow in a geriatric assessment in 85 subjects aged 65 years or over. These measures will be made by an actigraph and the software analysis BioVal. This technique will be compared with the standard technique (inclinometer). It will also be evaluated during this study, the ease of use and feedback.

Detailed description

The deterioration of the musculoskeletal system occurring in aging is a major cause of loss of autonomy and directly affects the quality of life of the individual. Support and appropriate rehabilitation for the patient's return home is essential. It requires physiotherapy assessment, which includes, among other things, a joint assessment with a measure passive range of motion. Physical therapists have different techniques to achieve these measures for each of them, the benefits (time, reliability) and disadvantages. Among them, the goniometer and inclinometer are technical references The main objective of the study is to validate the MotionPod and the software BioVal as valid tool for measuring range of motion of the elbow in a joint geriatric assessment. Secondary objectives are the study of the reproducibility of the measurement time and ease of use The measurement range of motion in the elbow in degree, estimated by actigraphy and software BioVal will be compared to those obtained with an inclinometer. The movements are examined successively flexion, extension, pronation and supination. The proportion of valid measurements will be calculated for each movement. The confidence interval 95% partner will also be calculated. Moreover, in order to judge the validity of actigraphy in all of these measures, the investigators will calculate the proportion of patients for which the measures are valid for all four movements and the confidence interval 95% partner. 85 patients aged 65 years or more will be recruited at the Cimiez hospital the CHU of Nice, in the services of short, medium and long geriatric stay

Interventions

DEVICEAssessment with inclinometer

joint assessment with inclinometer. The inclinometer used in this trial is Baseline® Bubble Inclinometer

DEVICEAssessment with actigraph

joint assessment with actigraph The actigraph used in this trial is the Motion Pod. It's an analysis and reeducation systems by biofeedback. The manufacturer is Movea.

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Prescription of physiotherapy . * Prescription of a passive joint assessment * Consent to participate in the study signed * person with a social security system

Exclusion criteria

* person with a pacemeker * patient with the inability to position the wrist straightness * patient with the inability to position the shoulder in neutral * metal prosthesis or osteosynthesis * patient with a joint debate \<20 ° * contraindicated warm up

Design outcomes

Primary

MeasureTime frameDescription
Inclinometer and actigraph assessmentelbow joint measures are done just at one time point, during the visitElbow joint measures by the inclinometer and the actigraph

Secondary

MeasureTime frameDescription
Assessment of easily useAssessment are done just at one time point, during the visitAssessment of easily use
Assessment comfort and utility of useAssessment are done just at one time point, during the visitAssessment of comfort and utility of use
measurement timeAssessment are done just at one time point, during the visitmeasurement time

Countries

France

Contacts

Primary ContactPhilippe ROBERT, PhD
robert.p@chu-nice.fr

Outcome results

None listed

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