A Study to Evaluate Patient Reported Outcome Measures in Children with Eye Conditions

Overview

About this study

The objectives of this study are:

  • To evaluate patient-reported quality of life and functional vision across the spectrum of pediatric eye conditions;
  • To assess change in patient-reported quality of life and functional vision over time;
  • To compare the impact of different treatments on quality of life and functional vision;
  • To assess change in patient-reported quality of life and functional vision in response to treatment;
  • To determine associations between quality of life / functional vision scores and specific clinical and demographic characteristics.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Children ages 0 to 17 years and one parent/legal guardian.
  • Current or previous diagnosis of an eye condition.
  • Any treatment status: pre-treatment, post-treatment, current treatment, no treatment.
  • Neurodevelopmental delay and/or systemic health disorders allowed.

Exclusion Criteria:

  • Individuals ≥ 18 years of age.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Erick Bothun, M.D.

Open for enrollment

Contact information:

Suzanne Wernimont CCRP

(507) 266-4326

Wernimont.Suzanne@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20516953

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