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Physical Activity Prescription for Post-ACL Reconstruction Recovery
Study Summary
This trial will investigate the effect of a physical activity prescription delivered through a mobile app on patient-reported outcomes and cartilage health in individuals 5-10 years post-ACL reconstruction.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I cannot or do not want to commit to the study's follow-up schedule.I am scheduled for a second surgery during the study.I am unable to communicate in English.
- Group 1: Physical Activity Prescription (PARx)
- Group 2: Usual Care
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
What is the current enrollment count for this clinical research?
"Affirmative. Clinicaltrials.gov reflects that this study, first posted on the 1st of November 2021, is actively searching for participants to enrol in their trial. In total 196 patients will be needed at a solitary medical centre."
Is the research open to individuals of advanced age?
"This research study is specifically targeting participants aged 21 to 32. Persons under 18 years old are limited to only 32 trials, whereas there are 587 for those over 65."
Are there any open enrollment slots for this research project?
"Affirmatively, this clinical trial is actively seeking patients. It was first published on November 1st 2021 and revised most recently the 28th of that same month."
Does my profile meet the requirements to join this experiment?
"To be eligible for this medical experiment, patients should have had a previous anterior cruciate ligament reconstruction and possess ages from 21 to 32. A total of 196 participants are needed for the study's success."
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