Study Stopped
Insufficient recruitment rate to reach the targeted number in June 2026
Combined Compared to Sequential Cognitive and Physical Training in Anterior Cruciate Ligament Reconstructed Individuals
DUACL
Dual-Task Training in an Immersive Environment Compared to Single Task Training in Anterior Cruciate Ligament Reconstructed Individuals
1 other identifier
interventional
2
1 country
2
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 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
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 13, 2025
CompletedFirst Posted
Study publicly available on registry
February 25, 2025
CompletedStudy Start
First participant enrolled
June 5, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 12, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 8, 2025
CompletedDecember 8, 2025
December 1, 2025
7 days
February 13, 2025
December 1, 2025
Conditions
Keywords
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
EXPERIMENTALSingle task training
ACTIVE COMPARATORInterventions
Combined simultaneous physical and cognitive training in an immersive environment
Eligibility Criteria
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
- Michelle C. Haaslead
- Kantonsspital Winterthur KSWcollaborator
- ZHAW DIZH Fellowship Programcollaborator
Study Sites (2)
KSW Kantonsspital Winterthur
Winterthur, 8000, Switzerland
ZHAW Zurich University of Applied Sciences
Winterthur, 8000, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
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.