UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000062973
Receipt number R000071974
Scientific Title Comparison of the Kinematic Characteristics of Real Dart Throwing and Dart-like Movements in a Virtual Reality Environment: An Exploratory Crossover Study Using Markerless Three-Dimensional Motion Analysis
Date of disclosure of the study information 2026/09/18
Last modified on 2026/09/18 12:16:38

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

A study comparing how people move when throwing a real dart and when throwing a dart in virtual reality

Acronym

A study examining differences between throwing a real dart and making a dart-throwing movement in virtual reality

Scientific Title

Comparison of the Kinematic Characteristics of Real Dart Throwing and Dart-like Movements in a Virtual Reality Environment:
An Exploratory Crossover Study Using Markerless Three-Dimensional Motion Analysis

Scientific Title:Acronym

Comparison of the Kinematic Characteristics of Real Dart Throwing and Dart-like Movements in a Virtual Reality Environment:
An Exploratory Crossover Study Using Markerless Three-Dimensional Motion Analysis

Region

Japan


Condition

Condition

Adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study will compare the kinematic characteristics of real-world dart-throwing movements and dart-like movements performed in a Virtual Reality (VR) environment among able-bodied adult university students, using markerless three-dimensional motion analysis, to explore to what extent movements performed in the VR environment reflect those involving actual objects. Furthermore, as a secondary objective, the study will examine the relationship between performance on the dart task under real-world conditions and kinematic indicators.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Differences in the range of motion of the elbow joint during the throwing phase between real-world darts and VR conditions

Key secondary outcomes

1. Peak values of elbow joint angular velocity under each condition
2. Inter-trial variability of kinematic indicators under each condition
3. Performance on the darts task under the real-darts condition (distance from the centre point for each throw)
4. Relationship between performance on the darts task and kinematic indicators under the real-darts condition
5. Subjective comparison of the real-darts condition and the VR condition based on a post-measurement questionnaire


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Real-Dart Conditions
Participants perform dart-throwing movements whilst standing, using real darts. After 3-5 practice throws to familiarise themselves with the task, they carry out 10 throws as the main trial. The throwing distance, target height and standing position are kept as consistent as possible. Movements of the upper limbs and trunk during the throwing motion are recorded using a markerless three-dimensional motion analysis system.
Under the real darts condition, the landing position of the dart for each throw is recorded, and the distance from the centre point is measured. The average distance from the centre point across the 10 throws is used as the performance score for the dart task under the real darts condition. Furthermore, the variability in performance is explored using the distance from the centre point for each throw.

Interventions/Control_2

VR Conditions
Participants will perform dart-like movements within a VR environment using a Meta Quest 2 and its dedicated controllers. The application used will be On Target VR Darts. After 3-5 practice throws to familiarise themselves with the task, participants will perform 10 throws as the main trial. During the VR condition, the research staff will monitor the participants' condition via an external monitor or by visual observation, and the trial will be stopped immediately should dizziness, discomfort or unsteadiness occur. Even under the VR condition, movements of the upper limbs and trunk during the dart-throwing-like movements will be recorded using a markerless 3D motion capture system.

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

65 years-old >=

Gender

Male and Female

Key inclusion criteria

1. Individuals aged 18 or over at the time of obtaining consent
2. Individuals with no obvious impairment in the movement of their upper limbs and trunk in daily life
3. Individuals capable of participating in both the real-world darts condition and the VR condition
4. Individuals from whom written consent was obtained of their own free will, following a full explanation of the study

Key exclusion criteria

1. Individuals with severe pain or restricted movement in the upper limbs, trunk or neck.
2. Individuals with a history of, or current symptoms of, musculoskeletal or neurological disorders that affect throwing movements.
3. Individuals for whom it is considered difficult to perform the VR or darts tasks due to visual impairment or vestibular dysfunction.
4. Individuals who are highly likely to experience severe dizziness, discomfort, headaches, nausea, etc., as a result of using VR equipment.
5. Individuals with competitive experience in darts.
6. Individuals for whom it is difficult to understand the research tasks or to obtain informed consent.
7. Any other individuals deemed unsuitable as research participants by the principal investigator.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Jun
Middle name
Last name Iwanami

Organization

Shinshu university

Division name

School of Health Sciences

Zip code

3908621

Address

3-1-1, Asahi, Matusmoto, Nagano, Japan

TEL

0263372406

Email

iwanami@shinshu-u.ac.jp


Public contact

Name of contact person

1st name Jun
Middle name
Last name Iwanami

Organization

Shinshu university

Division name

School of Health Sciences

Zip code

3908621

Address

3-1-1, Asahi, Matusmoto, Nagano, Japan

TEL

0263372406

Homepage URL


Email

iwanami@shinshu-u.ac.jp


Sponsor or person

Institute

Shinshu University

Institute

Department

Personal name

Jun Iwanami


Funding Source

Organization

Shinshu University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Committee of Shinshu University School of Medicine

Address

3-1-1, Asahi, Matusmoto, Nagano, Japan

Tel

0263354600

Email

shinshu@esct.bvits.com


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2026 Year 09 Month 18 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2026 Year 09 Month 09 Day

Date of IRB

2026 Year 09 Month 09 Day

Anticipated trial start date

2026 Year 10 Month 01 Day

Last follow-up date

2030 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2026 Year 09 Month 18 Day

Last modified on

2026 Year 09 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071974