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24 Month Follow-up of Patients With Osgood Schlatter (OSD)

A Prospective Investigation of Osgood Schlatter With 24 Month Follow-up

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03589001
Enrollment
51
Registered
2018-07-17
Start date
2018-07-10
Completion date
2019-02-28
Last updated
2019-07-02

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

Conditions

Apophysitis, Osgood-Schlatter Disease

Brief summary

Osgood Schlatter is a common knee condition, affecting approximately 10% of adolescents. OSD is thought to be a growth related pain conditon, and thus resolve after maturation. Despite this, there a lack of prospective data investigating whether this is in fact the case.

Detailed description

This is a prospective cohort study of 51 adolescents (aged 10-14 at baseline) with Osgood schlatter. Participants are followed for two years.

Interventions

OTHERActivity modification

Activity modification, exercises and gradual return to sport

Sponsors

Aalborg University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* 10-14 years of age * Pain at tibial tuberosity during two or more of the following activities: Sitting with a bent knee, squatting, running, jumping or stair ambulation * Pain during palpation of tibial tuberosity * Knee pain for 6 weeks or more

Exclusion criteria

* Other knee conditions that may manifest as anterior knee pain (Patellofemoral pain, iliotibial band syndrome, sinding-larson-johanson disease). * Previous surgery * Pain from the hip or back that interferes with activities of daily living. * Habitual patella luxations * Clinical suspicion of meniscal lesion

Design outcomes

Primary

MeasureTime frameDescription
Current knee pain24 monthsParticipants self-report if they still have knee pain

Secondary

MeasureTime frameDescription
Pain intensity24 monthsWorst pain in the previous week measured on a visual analogue scale (VAS) from 'no pain' to 'worst imaginable pain'
Pain frequency24 monthsFrequency of knee pain divided into (almost daily, several times per week, weekly, monthly, rarely, never)
Duration of being pain-free24 monthsThose who no longer have knee pain will be asked how long since their knee pain resoved
Medical attention24 monthsParticipants will be asked to report if they sought medical attention outside of the intervention
Use of pain killers24monthsParticipants will be asked if they use painkillers to manage their knee pain (y/n). If yes, they will be asked how often.
Sports participation24 monthsParticipants will report if they participate in sport. If yes how often and how much/week. They will also report if they have reduced sports participation due to knee pain.
Health Related quality of life24 monthsHealth related quality of life assessed by EQ 5D 3L Y (EuroQol, 5 dimensions, 3 levels for youth). Minimum 0, maximum 1, with higher values indicating higher quality of life.
Sleep24 monthsParticipants will be asked if they find it hard to sleep because of their knee pain (not at all, some nights, most nights).
knee injury and osteoarthritis outcomes score (KOOS) sport and activity subscale24 monthsknee injury and osteoarthritis outcomes score (KOOS) subscale sport and activity. Minimum 0 points, maximum 100points, with 100 points being the best possible score.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026