Reducing Disparities in Knee Arthroscopy for Adolescents

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14-18
SponsorAnn & Robert H Lurie Children's Hospital of Chicago

About this trial

Hundreds of thousands of youth athletes require surgery for knee injuries annually. The incidence of operative knee injuries has skyrocketed, but surgery can be delayed due to late recognition and barriers, such as insurance, language, and difficulty navigating the healthcare system. Delays may have lifelong effects, including arthritis, persistent instability, poor patient reported outcomes, and reoperation. There is little patient-centered research on barriers to orthopaedic care, and none on interventions to reduce disparities in pediatric sports medicine. This study will focus on Hispanic children, a growing population nationally and 38% of the Chicago's children, who are at increased risk of delayed knee surgery and its sequelae compared to white, non-Hispanic patients. The overall objectives are to identify barriers to timely knee surgery in Hispanic athletes and develop an intervention to implement evidence on expedient treatment. The aim of this study is to evaluate feasibility, acceptability, and appropriateness of a culturally-tailored intervention in a pilot study of Hispanic youth soccer leagues. The proposed study will drive creation of a future community trial of a culturally-tailored intervention.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Predominantly Hispanic soccer team

Players between 14-18 years of age

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Educational program and patient navigator

    Behavioral

    Players, coaches, and families randomized to the intervention arm will participate in a brief evidence-based presentation on surgical knee injuries led by a bilingual navigator and be encouraged to contact the navigator with injury concerns throughout the season.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Intervention armExperimental treatment 1 intervention
Group B: Control armNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Feasibility of Intervention Measure, Intervention Appropriateness Measure, and Acceptability of Intervention Measure

The primary outcomes of interest are intervention feasibility, appropriateness, and acceptability, as measured by these three brief, reliable, and valid tools. They include a total of 12 items using a 5-point Likert scale).

Time frame
One soccer season

Secondary outcomes

Other outcomes

Sponsors and contacts

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Ann & Robert H Lurie Children's Hospital of Chicago

Lead sponsor

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: