ClinicalTrials.Veeva

Menu

KinectROM Application for Assessing Range of Motion in Upper and Lower Extremity: A Development and Validation Study

S

Saime Nilay Arman

Status

Completed

Conditions

Range of Motion

Treatments

Device: Assessment of Range of Motion with Kinect Controller

Study type

Interventional

Funder types

Other

Identifiers

NCT03731507
IstanbulUC

Details and patient eligibility

About

The aim of the study is to investigate the validity and reliability of KinectROM application for objectively evaluating range of motion (ROM)

Full description

The application KinectROM called has been developed for assessing ROM with Kinect controller by our team. So, shoulder, elbow, knee, hip and ankle ROM measurements will be made with universal goniometer and developed KinectROM application.

Enrollment

45 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

inclusion Criteria: -Healthy individuals with 18-40 years

Exclusion Criteria:

-Have any limited extremity between the ages of 18-40 years.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 1 patient group

Range of motion in upper extremity
Experimental group
Description:
Assessment of shoulder: flexion/extension, abduction/adduction, internal/external rotation, elbow flexion/extension, hip: flexion/extension, abduction/adduction, internal/external rotation, knee: flexion/extension, ankle: dorsal flexion/plantar flexion
Treatment:
Device: Assessment of Range of Motion with Kinect Controller

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems