AzTrials
AzTrials

Virtual Reality TherapyVRSRNCT07110649

Virtual Reality Rehabilitation for Shoulder Injuries in Female College Basketball Players

A study testing Virtual Reality Rehabilitation Group and Traditional Rehabilitation Group in people with Virtual Reality Therapy, run by Jiarong Wang at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study aims to evaluate the effectiveness of virtual reality technology in the rehabilitation of shoulder injuries in college women's basketball players. We hypothesise that rehabilitation training using a virtual reality system can improve the range of motion of the shoulder joint more effectively than… Read more about this study

Who is it for?
Ages 18 to 24 years, women only
Conditions the study is for
Virtual Reality Therapy
What is being tested?
Virtual Reality Rehabilitation Group and Traditional Rehabilitation Group
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteChina
Study dates
15 Jul 2024to 16 May 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 24 years
  • Women only
  • No healthy volunteers
  • Adult

Eligible participants are female college basketball players between the ages of 18 and 24 who have limited shoulder range of motion (ROM limitation) as confirmed by standardized clinical assessment. Participants must regularly engage in basketball training and have no history of shoulder surgery. Individuals will be excluded if they have neurological disorders or other medical conditions that may interfere with virtual rehabilitation, a history of vertigo or intolerance to virtual reality environments, or severe shoulder instability or injuries that prevent participation in rehabilitation training.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Sanming Medicaand Polytechnic Vocational College

    Sanming, Fujian, 415000

Other trials in China

About this study

Official title: Experimental Study on the Improvement of Shoulder Range of Motion in College Women Basketball Players by Virtual Reality Technology

This study aims to evaluate the effectiveness of virtual reality technology in the rehabilitation of shoulder injuries in college women's basketball players. We hypothesise that rehabilitation training using a virtual reality system can improve the range of motion of the shoulder joint more effectively than traditional physical therapy methods and help athletes return to optimal condition. The study will compare the effects of virtual reality training, traditional rehabilitation training, and no intervention group.

Read the detailed description

To explore the intervention effects of virtual reality (VR) technology in shoulder injuryrehabilitation and its feasibility and practical value in college students 'sports recovery, thisstudy focuses on the theme of "The Therapeutic Effects of Virtual Reality Technology onShoulder lnjuries in Chinese University Basketball Players." A nine-week sports rehabilitationexperimental study was conducted. in line with the policy spirit of integrated development ofphysical education and health in Fujian Province's universities and the research direction ofour university's sports discipline, the project team collaborated with experts both inside andoutside the campus to conduct rehabilitation training experiments for a group of eligible female basketball players from Chinese universities.The study involved 45 female basketball players from universities in Fujian Province, allof whom experienced varying degrees of shoulder joint mobility limitations. Based on theiathletic abilities and injury severity, the participants were randomly divided into three groupsthe VR rehabilitation group, the traditional rehabilitation group, and the control group, with 15participants in each group. The VR rehabilitation group underwent immersive virtual realitytraining, which included exercises to increase joint range of motion and simulate specificbasketball movements. The traditional rehabilitation group received conventional physicatherapy and manual training. The control group did not receive any form of intervention.Statistical methods were used to compare and analyze the effectiveness of differentintervention methods in improving shoulder joint mobility. The experiment also combined on-site rehabilitation records and performance feedback to comprehensively evaluate theapplication prospects of virtual reality rehabilitation in sports medicine.

Being tested
Virtual Reality Rehabilitation Group, Traditional Rehabilitation Group
Keywords
VR, shoulder, female basketball player

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Virtual Reality Rehabilitation GroupDevice

    Also called PICO3

    Conducted in three progressive stages using VR games: improving ROM, strengthening shoulder muscles, and simulating game scenarios.

  • Traditional Rehabilitation GroupOther

    Used conventional physical therapy methods based on established rehabilitation programs.

Study groups in NCT07110649
Study groupRoleWhat they receive
Virtual Reality Rehabilitation GroupExperimentalParticipants in this group will receive immersive virtual reality rehabilitation training, which includes exercises designed to improve shoulder joint range of motion and simulate basketball-specific movements.
Receives: Device: Virtual Reality Rehabilitation Group
Traditional Rehabilitation GroupActive comparatorParticipants in this group will undergo conventional rehabilitation therapy, including manual therapy and exercises aimed at improving shoulder joint mobility.
Receives: Other: Traditional Rehabilitation Group
Control GroupNo interventionParticipants in this group will not receive any rehabilitation intervention and will only be monitored for natural recovery.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from Baseline in Shoulder Joint Range of Motion After 9-Week Rehabilitation

    The primary outcome of this study is the change in shoulder joint range of motion (ROM) across five directions: flexion, abduction, extension, internal rotation, and external rotation. Shoulder ROM will be measured using a digital goniometer with ±1° accuracy, following standardised protocols from the American Academy of Orthopaedic Surgeons (AAOS). The normal ROM values for shoulder movement are as follows: Flexion (0°-180°), Abduction (0°-180°), Extension (0°-60°), Internal Rotation (0°-70°), and External Rotation (0°-90°). A positive change indicates an improvement in shoulder joint mobility from baseline to post-intervention.

    Measured: From baseline assessment to the end of 9-week rehabilitation period

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Aug 2025
  2. Study start15 Jul 2024
  3. Primary completion13 Sep 2024
  4. Study completion16 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Virtual Reality Rehabilitation Group: Participants in this group will receive immersive virtual reality rehabilitation training aimed at improving shoulder joint mobility and basketball-specific movements. Traditional Rehabilitation Group: Participants in this group will undergo conventional physical therapy and manual training for shoulder joint rehabilitation. Control Group: Participants in this group will not receive any intervention and will be monitored for natural progression. Each group will consist of 15 participants, and the study will last for a total of 9 weeks.
Masking
None (open label)
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07110649
Sponsor's protocol ID
SMAPVC16042024
Other IDs
No External Funding
Acronym
VRSR
Status last verified
Jul 2025
First submitted
23 Jul 2025
Last updated
7 Aug 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Due to privacy concerns and the nature of the data, individual participant data will not be shared with other researchers. All data will be kept confidential and used only for the purpose of this study. However, if necessary, data can be made available upon request for academic or research purposes, but will not be shared for commercial use.

Publications

  • Morikawa LH, Tummala SV, Brinkman JC, Crijns TJ, Lai CH, Chhabra A. Shoulder and Elbow Injuries in National Basketball Association Athletes and Their Effects on Player Performance. Orthop J Sports Med. 2023 Oct 6;11(10):23259671231202973. doi: 10.1177/23259671231202973. eCollection 2023 Oct.

    PubMed 37810744

Questions about this trial

What is this clinical trial studying?

A study testing Virtual Reality Rehabilitation Group and Traditional Rehabilitation Group in people with Virtual Reality Therapy, run by Jiarong Wang at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from Baseline in Shoulder Joint Range of Motion After 9-Week Rehabilitation (time frame: From baseline assessment to the end of 9-week rehabilitation period). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07110649, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Aug 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in