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Effect on Active Knee Joint Stabilization of a Specific-Targeted Sensorimotor Training Compared to Standard Care in Persons After ACL Reconstruction - A Randomised Controlled Trial

Effect on Active Knee Joint Stabilization of a Specific-Targeted Sensorimotor Training Compared to Standard Care in Persons After ACL Reconstruction - A Randomised Controlled Trial - Sustainable Knee Health

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00033891
Enrollment
50
Registered
2024-05-23
Start date
2024-08-05
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M23.81

Interventions

Group 1: Sensorimotor training (8 weeks, 2 sessions per week, 30 minutes per session) in a 1:1 setting in former patients with an anterior cruciate ligament injury Group 2: Standard Care

Sponsors

Berner Fachhochschule für Gesundheit, Physiotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: - Physically active before injury (2x 45 min per week) - Clinically confirmed ACL rupture and reconstruction with a quadriceps tendon graft - Able to run, climbing stairs and perform one-leg jumps without perceiving pain during these movements - A limb symmetry index >90% for maximum strength performance capacity of knee extension & flexion and single leg hop performance

Exclusion criteria

Exclusion criteria: - Former knee pathology before initial ACL injury. This includes former ruptures to the ACL, meniscal tears and/or direct trauma to the cartilage as well as other knee ligament injury - Anamnestic exclusion of cardiac, neurologic, vestibular, or peripheral vascular diseases, acute infection, alcohol abuse, current pain medication, other injury of the lower extremity especially at the hip and ankle (in the last 6 months), back pain, trunk injury, thrombosis, pregnancy, dementia - Concussion within the past 6 months - Metal implants in the head or face - Severe headache/ migraine - Musculoskeletal disorders refraining from test protocol - Effusion with/without pain - Prone to seizures and/or blackouts

Design outcomes

Primary

MeasureTime frame
The primary outcome will be measured at measuring timepoint 0 (9-10 months after ACL reconstruction) and at the follow up measuring timepoint 1 (after 8 weeks of intervention). The primary outcome measure is measured by surface EMG and is defined as the neuromuscular activity during three voluntary tasks: - stairway walking (weight acceptance, M.semitendinosus) - jumping (postlanding, M.semitendinosus) - single leg stance with open, and closed eyes, respectively and one unvoluntary task: - artificial tibia translation/ stretch-reflex (medium latency response, M.semitendinosus)

Secondary

MeasureTime frame
The secondary outcomes will be measured at measuring timepoint 0 (9-10 months after ACL reconstruction) and at the follow up measuring timepoint 1 (after 8 weeks of intervention). EMG (Normalized EMG value [µV·µV-1], (% EMG)) : Time interval in gait and jump phase for stair ascent/descent - Preactivation (-150ms to initial touchdown) - Weight acceptance - Push-off Time interval after onset of tibia translation (hamstring stretch-reflex) - -50-0 ms background activity / preactivation - 20-40 ms short latency response (SLR) - 40-60 ms medium latency response (MLR) - 60-95 ms late latency response (LLR) EEG: Hamstring stretch-reflex - Theta at specific regions of interest  - Alpha-1 at specific regions of interest  - Alpha-2 at specific regions of interest  Single leg stance with open and closed eyes - Theta at specific regions of interest  - Alpha-1 at specific regions of interest  - Alpha-2 at specific regions of interest  Jumping height in m during single leg vertical jump Jumping distance in m during single leg triple hop Center of pressure excursion during single leg stances

Countries

Switzerland

Contacts

Public ContactHeiner Baur

Berner Fachhochschule für Gesundheit, Physiotherapie

heiner.baur@bfh.ch+41 31 848 45 15

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Sep 19, 2026