An Objective Measurement Method With The Leap Motion Sensor For Hand And Wrist's Range Of Motion

Developing An Objective Measurement Method With The Leap Motion Sensor For Hand And Wrist's Range Of Motion: Validity And Reliability Study

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03622645

Enrollment

Registered

2018-08-09

Start date

2017-01-13

Completion date

2018-09-01

Last updated

2018-11-06

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

Conditions

Range of Motion

Keywords

Range of motion, Wrist, Hand, Finger, Measurement

Brief summary

The aim of the study was to develop a low cost, clinically easy to use measurement method with the Leap motion sensor for objectively evaluating range of motion (ROM), and to investigate the validity and reliability of this application.

Detailed description

. Wrist flexion / extension, radial / ulnar deviation, supination / pronation, 1.-5. of the fingers DIP, PIP and MCP flexion / extension ROM measurements will be made with universal goniometer and developed Leap motion sensor (LMC) based measurement method. The study consists of two basic steps: 1. Development of measurement method with LMC Identification of normROM measurement procedure Identification of ROM measurement reporting Establishing the precursor version of the software of the measurement method Checking ROM measurement performance criteria and providing feedback Measuring the movement defined on 5 persons and providing feedback Creation of the last available version of the measurement method 2. Validity and reliability study Measurements of hand and wrist ROM with developed measurement method with LMC and universal goniometer for three times and calculation mean of three measurement for two methods

Interventions

DEVICEAssessment of Range of Motion with Leap Motion sensor

An ROM measurement method called as HandROM by us will be developed with leap motion sensor

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 40 Years

Healthy volunteers

Yes

Inclusion criteria

* Healthy individuals

Exclusion criteria

* Have any hand/wrist problems between the ages of 18-40 years.

Design outcomes

Primary

Measure	Time frame	Description
Range of Motion	Baseline	Wrist flexion / extension, radial / ulnar deviation, supination / pronation, 1. -5. DIP, PIP and MCP flexion / extension EHA measurements of the fingers will be made with universal goniometer and developed Leap motion sensor based measurement method.

Outcome results

None listed

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