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Physical Activity Prescription for Post-ACL Reconstruction Recovery

N/A
Recruiting
Led By Jane Thornton, MD PhD
Research Sponsored by Western University, Canada
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights

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.

Who is the study for?
This trial is for individuals who are 7 years post-ACL reconstruction surgery and part of the STAbiLiTY study. They must have internet and smartphone access, be stable enough to engage in physical activity, willing to follow up during the study period, and communicate in English.Check my eligibility
What is being tested?
The trial is testing a Physical Activity Prescription (PARx) intervention aimed at improving knee health after ACL reconstruction. It investigates whether regular prescribed exercise can prevent or delay osteoarthritis by promoting better cartilage health.See study design
What are the potential side effects?
While specific side effects aren't listed for PARx, increased physical activity could potentially lead to muscle soreness, joint pain, or exacerbation of existing knee issues if not done carefully.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
International Knee Documentation Committee (IKDC)
Secondary outcome measures
Knee Injury and Osteoarthritis Outcome Score
Physical Activity Evaluation using Global Physical Activity Questionnaire (GPAQ) and MyRecovery app
Three-dimensional Motion-captured Gait Biomechanics Analysis
+1 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Physical Activity Prescription (PARx)Experimental Treatment1 Intervention
Patients will be prescribed technology-based physical activity programming.
Group II: Usual CareActive Control1 Intervention
Patients will receive the usual care.

Find a Location

Who is running the clinical trial?

Western University, CanadaLead Sponsor
239 Previous Clinical Trials
57,287 Total Patients Enrolled
Jane Thornton, MD PhDPrincipal InvestigatorWestern University
1 Previous Clinical Trials
192 Total Patients Enrolled

Media Library

Physical Activity Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05152758 — N/A
Anterior Cruciate Ligament Reconstruction Research Study Groups: Physical Activity Prescription (PARx), Usual Care
Anterior Cruciate Ligament Reconstruction Clinical Trial 2023: Physical Activity Intervention Highlights & Side Effects. Trial Name: NCT05152758 — N/A
Physical Activity Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05152758 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

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."

Answered by AI

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."

Answered by AI

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."

Answered by AI

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."

Answered by AI
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~42 spots leftby Dec 2024