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临床试验/NCT05174182
NCT05174182已完成不适用

A Comparison of Two Different Treatment Approaches for Adolescents With Osgood Schlatter: A Randomized Controlled Superiority Trial (The SOGOOD Trial)

Hvidovre University Hospital2 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2022年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
试验地点
2
主要终点
Knee and Osteoarthritis Outcome Score for Children (KOOS-Child) 'Sport / Recreation' subscale change from baseline

研究概览

简要总结

The most common growth-related injury is Osgood Schlatter, which affects up to 1 in 5 physically active adolescents. It can cause long-term pain and potential discontinuation of sports and physical activity, with sequela well into adulthood. No effective conservative treatments have been documented, and clinical practice is characterized by a wealth of conflicting advice and modalities. A novel treatment approach has shown promising results in a small single-cohort study. Therefore, this study aims to compare this novel treatment with usual care in 10-16-year-old adolescents with Osgood Schlatter.

This single-center pragmatic, double-blinded, randomized, controlled superiority trial, will have a two-group parallel arm design. Participants will undergo 3 months of treatment, followed by 2 months of self-management with self-reported knee function (KOOS-child 'Sport/rec') at 5 months as the primary endpoint.

This trial comparing a novel treatment with usual care for adolescents with Osgood Schlatter could result in an evidence-based treatment ready for implementation in clinical practice, benefitting patients outcomes and clinicians.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

Participants: Participants are blinded to the actual contents of the two interventions before being allocated, and will remain blinded to the contents of the parallel intervention. They are also blinded to the superiority framework.

Care provider: Therapists delivering an intervention will likewise be blinded to the contents of the parallel intervention, and to the superiority framework.

Outcomes assessors: Staff collecting objective outcome data are blinded to group allocation of participants.

入排标准

年龄范围
10 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Tenderness on palpation of the tibial tuberosity or pain during resisted isometric knee extensions
  • Insidious onset of pain or swelling of the tibial tuberosity for ≥6 weeks
  • Provoked by at least 2 of the following positions or activities; prolonged sitting or kneeling, squatting, running, hopping/jumping, stair walking or during multidirectional sports
  • Clinical diagnosis of Osgood Schlatter
  • Markedly reduced sports participation OR severely affected by pain during sports participation

排除标准

  • Other primary pathology or complaints from other structures of the knee
  • Other injuries, complaints or illnesses that may cause disability, or specifically restricts levels of physical activity or sports participation
  • Previous surgery in the lower extremities or lumbar spine
  • Congenital deformities, device implants og cysts og tumors of the knee
  • Participants not willing to cease concomitant treatment
  • Participants and their parents not able to understand and communicate in written and verbal Danish

结局指标

主要结局

Knee and Osteoarthritis Outcome Score for Children (KOOS-Child) 'Sport / Recreation' subscale change from baseline

时间窗: 5 months (secondary timepoints: month 1, 2, 3, 8, 10, 12, 24, 48)

The scale contains 7 questions answered through a 0-4 likert scale. The scale is normalized to a 0-100 score with 100 be, with zero representing extreme knee problems and 100 representing no knee problems.

次要结局

  • Hours of Physical Activity(5 months)
  • Hours of Sports Participation(5 months)
  • Flaviis composite severity score change from baseline(5 months)
  • Anterior Knee Pain Provocation test change from baseline(5 months)
  • Pressure-pain threshold at the tibial tubercle change from baseline(5 months)
  • Patient Acceptable Symptom State change from baseline(5 months)
  • Pain Flare Intensity change from baseline(5 months)
  • Tendinosis signs change from baseline(5 months)
  • Kinesiophobia change from baseline(5 months)
  • Pain during knee extension strength test change from baseline(5 months)
  • Countermovement jump height change from baseline(5 months)
  • Patient-specific function scale change from baseline(5 months)
  • Knee and Osteoarthritis Outcome Score for Children (KOOS-Child) 'Quality of Life' Subscale change from baseline(5 months)
  • Frequency of Pain Flares(5 months)
  • Satisfaction with extent of sports participation change from baseline(5 months)
  • Global rating of Change(5 months)
  • Infrapatellar bursitis signs change from baseline(5 months)
  • Maximal isometric knee extension strength change from baseline(5 months)
  • Self-rated health change from baseline(5 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kasper Krommes

Senior Research Coordinator

Hvidovre University Hospital

研究点 (2)

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