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Live Feedback to Increase Adherence in Adolescents With Patellofemoral Pain

Efficacy of Live Feedback to Increase Objectively Monitored Adherence to Prescribed, Home-based, Exercise Therapy-dosage in 15 to 19 Year Old Adolescents With Patellofemoral Pain. A Randomized Controlled Superiority Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02674841
Enrollment
40
Registered
2016-02-05
Start date
2016-02-29
Completion date
2016-10-31
Last updated
2016-11-17

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

Conditions

Joint Diseases, Musculoskeletal Disorders, Patellofemoral Pain Syndrome

Keywords

Adolescent, Physical therapy modalities, Exercise intervention, Auditive feedback, Visual feedback

Brief summary

This study investigates if live feedback during home-based exercises will improve the ability to perform the exercises with the prescribed time under tension (TUT) per repetition compared with no feedback among adolescents with patellofemoral pain. The hypothesis is that adolescents who receive live feedback from BandCizer™ will have a mean TUT that is significantly closer to the prescribed TUT compared to the group not receiving feedback during the course of the intervention.

Interventions

OTHERFeedback on TUT

Access to live visual and auditory feedback on TUT and pulling force from an application on an iPad.

OTHERNo feedback on TUT

Access only to live visual feedback on pulling force from an application on an iPad.

OTHERExercise

3 exercises (knee extension, hip abduction and hip extension) using an elastic band with 3 sets of 10 repetitions at 10-12 RM 3 times a week for 6 weeks.

Sponsors

Aalborg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
15 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* 15 to 19 years of age * Anterior knee pain of non-traumatic origin which is provoked by at least two of the following activities: prolonged sitting with bended knees or kneeling, squatting, running, jumping or ascending or descending stairs * Tenderness on palpation of the peripatellar borders * Pain of more than 6 weeks duration * Worst pain during the previous week ≥ 30 mm on a 100 mm VAS

Exclusion criteria

* Concomitant pain from other structures in the knee (e.g. ligament, tendon or cartilage), the hip or the lumbar spine * Previous knee surgery * Patellofemoral instability

Design outcomes

Primary

MeasureTime frameDescription
Mean deviation from the prescribed TUT per repetition in seconds during the course of the interventionFrom 0-6 weeksThe mean deviation is calculated as the difference between actual TUT and prescribed TUT (8 seconds). E.g. if the actual TUT is 6.5 seconds, the deviation is 1.5 seconds

Secondary

MeasureTime frameDescription
The total number of repetitions performedFrom 0-6 weeks
Pulling force exerted per repetition measured in kilosFrom 0-6 weeksThis will be expressed as the maximum pulling force during each repetition
Isometric strengthAt baseline and at the 6 week follow upPresented as Nm/kg in x, y and z direction
Summary of resistanceFrom 0-6 weeksTotal pulling force exerted during the course of the intervention measured in kilos
Kujala Patellofemoral Scale-scoreAt baseline and at the 6 week follow upGives a score on patellofemoral pain ranging from 0 to 100 with 0 as complete disability and 100 as fully functional
Global rating of changeAt the 6 week follow upSelf-reported recovery on a 7-point Likert scale ranging from much improved to much worse
Pain measured on a 100 mm VASFrom 0-6 weeksIs entered into the app by the adolescent before and after each exercise

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026