NCT06845150

Brief Summary

The goal of this clinical trial is to investigate changes in cognitive and physical performance after 10 weeks of dual or single task training in anterior cruciate ligament (ACL) reconstructed individuals. The main questions it aims to answer are:

  • Does cognitive performance in ACL reconstructed individuals change after multiple training sessions incorporating single versus dual-task?
  • Does physical performance and intrinsic motivation for training change over the course of 10 weeks when performing single versus dual-task training sessions?
  • What movement patterns do ACL reconstructed individuals show during a dual-task training in an immersive environment? Researchers will compare a combined dual-task training (combined physical and cognitive training) to a single task training (physical and cognitive training separately) to see if there are changes on cognitive performance depending on the training type. Participants will:
  • Perform dual-task or single task training twice per week for 10 weeks
  • Visit the clinic before and after the training period for tests
  • Visit the movement laboratory once for analysis of movement patterns

Trial Health

57
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Trial Health Score

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

Enrollment
2

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 13, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

February 25, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

June 5, 2025

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 12, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 8, 2025

Completed
Last Updated

December 8, 2025

Status Verified

December 1, 2025

Enrollment Period

7 days

First QC Date

February 13, 2025

Last Update Submit

December 1, 2025

Conditions

Keywords

motor-cognitive trainingdual-task traininganterior cruciate ligament injuryreturn to competition

Outcome Measures

Primary Outcomes (2)

  • Interference

    Measured by the difference in reaction time of congruent and incongruent stimuli of the Flanker task.

    Baseline, after 5 weeks of training, after 10 weeks of training

  • Response inhibition

    Measured by the accuracy of Go/No-Go-stimuli

    Baseline, after 5 weeks of training, after 10 weeks of training

Secondary Outcomes (6)

  • Jumping performance - contact time

    Baseline and after 10 weeks of training

  • Jumping performance - peak force

    Baseline and after 10 weeks of training

  • Strength

    Baseline and after 10 weeks of training

  • Intrinsic motivation

    At the end of each training session (2x/week for 10 weeks)

  • Kinematics and kinetics of the lower extremities

    During dual-task training in an immersive environment

  • +1 more secondary outcomes

Other Outcomes (5)

  • Kujala

    Baseline and after 10 weeks of training

  • ACL-Return to Sport after Injury Scale

    Baseline and after 10 weeks of training

  • Tegner Activity Scale

    Baseline and after 10 weeks of training

  • +2 more other outcomes

Study Arms (2)

Dual-task training

EXPERIMENTAL
Other: Dual-task training

Single task training

ACTIVE COMPARATOR
Other: Single task training

Interventions

Combined simultaneous physical and cognitive training in an immersive environment

Dual-task training

Sequential cognitive and then physical training

Single task training

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • years old
  • At least 6 months after ACL injury
  • Surgically reconstructed ACL
  • At least 2 hours of sports participation before the injury
  • Written consent of the attending surgeon to perform intensified training methods including one-legged jumps at 6 months after surgery after the first visit
  • Ability to give informed consent as documented by signature
  • Ability to understand instructions in German or English
  • BMI \< 28 kg/m\^2
  • Availability to take part in at least 70% of all training sessions

You may not qualify if:

  • Surgery on the contralateral leg during the last 12 months
  • Acute or chronic musculoskeletal, neurological, or cardiopulmonary disorders
  • Unadjusted vision problems
  • Concussion during the last 6 months
  • Pregnancy
  • Breastfeeding
  • Amputation
  • Inflammatory pain or swelling during exercising

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

KSW Kantonsspital Winterthur

Winterthur, 8000, Switzerland

Location

ZHAW Zurich University of Applied Sciences

Winterthur, 8000, Switzerland

Location

MeSH Terms

Conditions

Anterior Cruciate Ligament Injuries

Condition Hierarchy (Ancestors)

Knee InjuriesLeg InjuriesWounds and Injuries

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
concealed allocation of group
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Research Associate

Study Record Dates

First Submitted

February 13, 2025

First Posted

February 25, 2025

Study Start

June 5, 2025

Primary Completion

June 12, 2025

Study Completion

October 8, 2025

Last Updated

December 8, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

Individual participant data will be shared if ethically and legally possible.

Locations