NCT07461025

Brief Summary

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

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

First Submitted

Initial submission to the registry

February 26, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

March 10, 2026

Completed
14 days until next milestone

Study Start

First participant enrolled

March 24, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

April 1, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

February 26, 2026

Last Update Submit

March 26, 2026

Conditions

Keywords

dual task

Outcome Measures

Primary Outcomes (2)

  • Cognitive dual-task cost

    Dual-task cost with the different modalities are operationalized by reaction time.

    Measurement session 1 (day 0) and session 2 (days 6-90)

  • Exergaming performance

    Operationalized as task success rate

    Session 2 (days 6-90)

Secondary Outcomes (8)

  • Motor dual-task cost

    Session 1 (day 0)

  • Countermovement Jump

    Session 1 (day 0) and session 2 (day 6-90)

  • ProAgility Test

    Session 1 (day 0) and session 2 (day 6-90)

  • Y-Balance Test

    Session 1 (day 0) and session 2 (days 6-90)

  • Joint Angle

    Session 1 (day 0) and session 2 (day 6-90)

  • +3 more secondary outcomes

Study Arms (1)

Dual-Task paradigms

EXPERIMENTAL

All participants are exposed to the same dual-task paradigms described in the intervention.

Other: different dual-task paradigms

Interventions

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.

Dual-Task paradigms

Eligibility Criteria

Age18 Years - 34 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

ZHAW Zurich University of Applied Sciences

Winterthur, Canton of Zurich, 8400, Switzerland

RECRUITING

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 26, 2026

First Posted

March 10, 2026

Study Start

March 24, 2026

Primary Completion

July 1, 2026

Study Completion

August 1, 2026

Last Updated

April 1, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share

Pooled data of participants will be shared on a repository if consent is given by the participants.

Time Frame
Within one year after completion of the study.
Access Criteria
The access conditions will be defined in the license statement adjacent to the dataset.

Locations