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Psychologically Informed Education for Patellofemoral Pain Syndrome

N/A
Waitlist Available
Led By Mitchell Selhorst, DPT, PHD
Research Sponsored by Nationwide Children's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 1 week, 3 weeks (18-24 days post-evaluation), 6 weeks (39-46 days post-evaluation), and 3 months]
Awards & highlights

Study Summary

This trial is studying whether psychological factors affect pain and physical performance in teens with patellofemoral pain. Participants will complete surveys and be assigned to either watch educational videos or a control group. Follow-up surveys will be completed to measure pain, psychological beliefs, and functional ability.

Eligible Conditions
  • Patellofemoral Pain Syndrome
  • Chronic Knee Pain
  • Patellofemoral Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 1 week, 3 weeks (18-24 days post-evaluation), 6 weeks (39-46 days post-evaluation), and 3 months]
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 1 week, 3 weeks (18-24 days post-evaluation), 6 weeks (39-46 days post-evaluation), and 3 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
Knee
Secondary outcome measures
Change in Fear-Avoidance Beliefs
Change in Kinesiophobia
Change in Numeric Pain Rating Scale
+2 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Psychologically Informed Video SeriesExperimental Treatment1 Intervention
This 3 part educational video series will teach participants how the body processes nociception and experiences pain, and pain does not mean tissues are being damaged. Additionally we will use the framework called the "Common Sense Model of Self-Regulation" which advocates for education to address five cognitive dimensions: (1) identity (the effort to evaluate symptoms and label the illness); (2) cause (the subjectively formulated belief of what is causing the symptoms); (3) time-line (the patient's perception of how long the problem will last); (4) consequences (the patient's predictions of how the illness will affect them in different areas of their life); and (5) controllability (the patient's belief regarding their outcome and personal ability to change it); Simple methods of cognitive restructuring; and how to respond to activity-related pain.
Group II: Biomedical Education Video SeriesActive Control1 Intervention
Participants in the control (biomedical education) group will watch a series videos on the iPad equal in length to the psychologically informed video series. The control video will discuss basic anatomy of the knee and provide no psychosocial education or positive reinforcement about their condition, basic strengthening exercises and proper lower extremity mechanics

Find a Location

Who is running the clinical trial?

Nationwide Children's HospitalLead Sponsor
341 Previous Clinical Trials
5,220,435 Total Patients Enrolled
3 Trials studying Patellofemoral Pain Syndrome
153 Patients Enrolled for Patellofemoral Pain Syndrome
Mitchell Selhorst, DPT, PHDPrincipal Investigator - Nationwide Children's Hospital
Nationwide Children's Hospital

Frequently Asked Questions

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

Who would be a good candidate to enroll in this research project?

"The target population for this study are adolescents aged 12 to 18 who suffer from patellofemoral pain. Key inclusion criteria are as follows: the candidate must have pain around or behind the kneecap which is made worse by at least one activity that puts weight on the knee when it is bent (for example, squatting, going up and down stairs, jogging/running, or hopping/jumping)."

Answered by AI

Would elderly citizens be able to enroll in this particular program?

"The age bracket for participants in this trial are those that are 12 years old or older, but have not yet celebrated their 18th birthday."

Answered by AI
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~17 spots leftby Apr 2025