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Recruiting NCT07461025

Relationship Between Modality-specific Dual-task Performance and Immersive Exergaming Outcomes in Healthy Athletes

No phase Interventional Healthy Athlete

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: different dual-task paradigms.
Who it may be relevant to
Registry conditions: Healthy Athlete. Basic parameters: 18 years — 34 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this clinical trial is to provide a more specific understanding of which dual task conditions elicit changes in either motor or cognitive performance. A dual-task is a simultaneously performed motor and cognitive task. Exergaming describes physically active gaming. The main questions the study aims to answer are: * Can performance in visual and auditory dual-task paradigms explain performance in an immersive exergaming task in healthy athletes? * How are exergaming scores associated with athletic performance tests? * What biomechanical movement patterns are shown during dual-tasks? Researchers will also compare performance of those experienced with jumping and those inexperienced with jumping. Participants will: * Complete two sessions performing athletic performance tests, cognitive tasks, and different dual-tasks while their movement pattern is recorded * Complete questionnaires on load, stress, and sleep during the sessions

Detailed description

The two sessions last each approximately 2 hours and take place within one to 12 weeks. Both sessions involve measurement of biomechanical movement patterns with motion capture.

Interventions

  • Other different dual-task paradigms
    Participants will perform combined motor-cognitive tasks. During the first session balancing and bilateral jumping will be combined with an additional auditory or visual cognitive task. During the second session participants will do a combined motor-cognitive task in exergaming.

Primary outcome measures

  • Cognitive dual-task cost [Time frame: Measurement session 1 (day 0) and session 2 (days 6-90)]
  • Exergaming performance [Time frame: Session 2 (days 6-90)]
Secondary outcome measures (8)
  • Motor dual-task cost [Time frame: Session 1 (day 0)]
  • Countermovement Jump [Time frame: Session 1 (day 0) and session 2 (day 6-90)]
  • ProAgility Test [Time frame: Session 1 (day 0) and session 2 (day 6-90)]
  • Y-Balance Test [Time frame: Session 1 (day 0) and session 2 (days 6-90)]
  • Joint Angle [Time frame: Session 1 (day 0) and session 2 (day 6-90)]
  • Joint Moment [Time frame: Session 1 (day 0) and session 2 (day 6-90)]
  • Ground Reaction Force [Time frame: Session 1 (day 0) and session 2 (day 6-90)]
  • Center of pressure [Time frame: Session 1 (day 0) and session 2 (day 6-90)]

Eligibility criteria

Inclusion criteria

  • age between 18 and 34 years
  • self-reported recreationally or competitively active (more than 2 hours per week)
  • self-reported ability to complete change of direction, balancing, and jumping tasks
  • capacity to sign informed consent
  • ability to understand German

Exclusion criteria

  • acute injury in the last 6 months resulting in missing more than 3 training sessions
  • severe comorbidity or condition which would prohibit performance of the lsted testing tasks
  • self-reported pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

Switzerland · 1 center
  • ZHAW Zurich University of Applied Sciences — Winterthur

Identifiers

NCT: NCT07461025 · DUTACO

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗