Multimodal Assessment of Knee Conditions in Rehabilitation
NCT ID: NCT03608189
Last Updated: 2018-07-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
20 participants
OBSERVATIONAL
2018-08-01
2018-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Early Treatment Based Neuroscience Education in Knee
NCT05440890
Motor Imagery After Reconstruction of the Anterior Cruciate Ligament
NCT05168033
Neuromuscular Rehab for ACL Reconstruction: Knee Function & Brain Plasticity
NCT07243860
Effect of Kinesio Tape on Motor Function in Subjects With ACL Rupture
NCT04954924
The Effects of Cognitive Dual-Tasking in Later Stages of Rehabilitation After ACL Reconstruction
NCT06206200
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
ACL injury subjects
Subjects with anterior cruciate ligament injuries.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Ages 18-40
* Female
Exclusion Criteria
* BMI over 40
* Contraindications to MRI
18 Years
40 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Oulu
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Simo Saarakkala, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Oulu
Osmo Tervonen, Ph.D., M.D.
Role: STUDY_DIRECTOR
Oulu University Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Oulu
Oulu, North Ostrobothnia, Finland
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
24302214
Identifier Type: OTHER
Identifier Source: secondary_id
24302214-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.