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

C

Centre Hospitalier Universitaire de Nice

Status

Unknown

Conditions

Geriatric Disorder

Treatments

Device: Assessment with inclinometer
Device: Assessment with actigraph

Study type

Interventional

Funder types

Other

Identifiers

NCT01462760
11-PP-11

Details and patient eligibility

About

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.

Full 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

Enrollment

85 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

85 participants in 2 patient groups

First assessment: inclinometer
Other group
Description:
First assessment: inclinometer Second assessment: actigraph and inclinometer
Treatment:
Device: Assessment with inclinometer
first: Inclinometer and actigraph
Other group
Description:
first: Inclinometer and actigraph second: inclinometer
Treatment:
Device: Assessment with inclinometer
Device: Assessment with actigraph

Trial contacts and locations

1

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Central trial contact

Philippe ROBERT, PhD

Data sourced from clinicaltrials.gov

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