Extended Reality Cognitive and Breathing Training With Eye Tracking for Attention and Stress Regulation in Adolescent Basketball Players
XR-CogBreathe
2 other identifiers
interventional
81
1 country
2
Brief Summary
This study examines whether virtual reality (VR) technology can serve as a supplementary training tool for adolescent basketball players. Two types of 6-week VR training were tested alongside regular basketball practice: one targeting attention and decision-making (cognitive training), and one targeting breathing patterns (slow diaphragmatic breathing). A third group continued regular training without any VR component. Participants were basketball players aged 14-17 who trained at least three times per week. Before and after the 6-week period, all participants completed assessments measuring resting heart rate, heart rate variability, breathing function (CO₂ tolerance, breathing pattern), reactive stress tolerance, selective and sustained attention, and pre-competition anxiety. The primary aim was to evaluate feasibility - whether participants were willing to join and complete the sessions, whether the procedures worked as intended in a real training environment, and whether the study design is suitable for a larger future trial. The study was not designed to confirm effectiveness.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 7, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 22, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 22, 2025
CompletedFirst Submitted
Initial submission to the registry
September 30, 2026
CompletedFirst Posted
Study publicly available on registry
October 9, 2026
CompletedOctober 9, 2026
October 1, 2026
2 months
September 30, 2026
October 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Recruitment rate
Proportion of eligible athletes who provide consent and are enrolled in the study. Reported as the number enrolled divided by the number eligible.
During recruitment, up to 6 weeks
Randomization completion rate
Proportion of enrolled participants who are successfully allocated to one of the study arms. Reported as the number randomized divided by the number enrolled.
At baseline, before intervention initiation
Retention rate
Proportion of enrolled participants who complete the post-intervention assessment. Reported as the number completing follow-up divided by the number enrolled.
Baseline through 6-week post-intervention assessment
Intervention adherence
Attendance among participants allocated to either XR intervention arm. Reported as the number of intervention sessions completed out of 12 scheduled sessions, expressed as a percentage.
During the 6-week intervention period
Intervention acceptability
Post-intervention acceptability assessed using a study-specific 4-item questionnaire measuring task interest, mixed-reality excitement, motivation to perform tasks, and willingness to continue. Items are rated from 1 (completely disagree) to 5 (completely agree). Total score range: 4 (minimum) to 20 (maximum). Higher scores indicate greater acceptability. Report item scores and/or mean total score.
At 6 weeks (post-intervention)
Secondary Outcomes (17)
Selective attention - concentration performance level (d2-R SUMKL)
Baseline and 6 weeks
Sustained attention and processing speed - total correctly processed items (d2-R SUMBZO)
Baseline and 6 weeks
Omission errors - failures to mark target stimuli (d2-R SUMAF)
Baseline and 6 weeks
Commission errors - false responses (d2-R SUMVF)
Baseline and 6 weeks
Change from Baseline to 6 Weeks in Functional Breathing Pattern Proportion
Baseline and 6 weeks
- +12 more secondary outcomes
Study Arms (3)
Cognitive XR Training
EXPERIMENTALParticipants receive a 6-week XR cognitive and visuomotor training program in addition to their usual basketball training. They complete two 10-minute sessions per week, for a maximum of 12 sessions and 120 minutes of total exposure. Sessions are delivered at the participant's usual basketball-training venue.
Breathing XR Training
EXPERIMENTALParticipants receive a 6-week XR breathing and gaze-control training program in addition to their usual basketball training. They complete two 7-minute sessions per week, for a maximum of 12 sessions and 84 minutes of total exposure. Sessions are delivered at the participant's usual basketball-training venue.
Usual Basketball Training Control (No intervention)
NO INTERVENTIONParticipants continue their usual basketball training routine at their respective clubs. They complete baseline and post-intervention assessments on the same schedule as the intervention groups but receive no study-provided XR cognitive, visuomotor, or breathing training during the 6-week study period.
Interventions
Participants complete two 10-minute sessions weekly for 6 weeks (maximum 12 sessions; 120 minutes total exposure) using an HTC VIVE Focus Vision standalone head-mounted display with binocular eye tracking. While dribbling a real basketball, participants follow a moving virtual basketball with their gaze, avoid virtual obstacles, and respond to spatial and auditory cues within predefined court boundaries. Attention time is recorded when a valid gaze signal intersects the active target under the required spatial conditions. Difficulty progresses through target speed, obstacle number and movement, target switching, movement zones, whistle-controlled tasks, jumping obstacles, and spatialized sounds. A fixed pre-programmed level sequence is individually paced according to an on-target-time criterion. Research staff supervise baseline testing and the first two sessions; from week 2, participants use password-protected individual profiles independently.
Participants complete two 7-minute sessions weekly for 6 weeks (maximum 12 sessions; 84 minutes total exposure) using an HTC VIVE Focus Vision standalone head-mounted display. Seated within an approximately 1 × 1 m area, participants perform slow diaphragmatic breathing while completing a gaze-controlled virtual basketball-tracking task. Breathing pace progresses from 7 breaths/min in minute 1, to 6.5 breaths/min in minute 2, and 6 breaths/min during minutes 3-7, using a 40:60 inhalation-to-exhalation ratio. A handheld controller placed horizontally on the upper abdomen detects abdominal movement to estimate breathing phase and adherence. Accurate breathing increases virtual-player responsiveness and speed, whereas departures from the prescribed pattern reduce performance. Research staff supervise baseline testing and the first two sessions; from week 2, participants use password-protected individual profiles independently.
Eligibility Criteria
You may qualify if:
- Adolescent basketball players aged 14-17 years
- Organized basketball training for at least 5 years
- Training at least 3 times per week
You may not qualify if:
- Serious musculoskeletal injury or acute medical condition affecting sports performance in the previous month
- Severe orthopedic, neurological, cardiovascular, or other medical disorders
- Use of prescription medications affecting the central nervous system (e.g., psychotropic medication)
- Symptoms of visually induced motion sickness (VIMS): nausea, dizziness, headache, or disorientation before or during participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Riga Stradins Universitylead
- European Unioncollaborator
Study Sites (2)
Jūrmala Sport School Basketball Arena
Jūrmala, Latvia
Ventspils Basketball Arena
Ventspils, Latvia
Study Officials
- STUDY DIRECTOR
Agris Liepa, PhD
Riga Stradins University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant Intern; Junior Researcher (PhD Student)
Study Record Dates
First Submitted
September 30, 2026
First Posted
October 9, 2026
Study Start
November 7, 2025
Primary Completion
December 22, 2025
Study Completion
December 22, 2025
Last Updated
October 9, 2026
Record last verified: 2026-10
Data Sharing
- IPD Sharing
- Will not share