A Study of the Imaging, Genetics, Clinical Presentation, Diagnostics, and Progression of Chronic Traumatic Encephalopathy

Overview

Información sobre este estudio

The purpose of this study is to collect and analyze neuroimaging, genetic markers, and clinical presentations and progressions of chronic traumatic encephalopathy to develop methods of diagnosing the disease during life. 

 

 

 

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

Former NFL Players

  • English as primary language.
  • No MRI or Lumber Puncture (LP) contraindications.
  • Have played ≥ 12 years of organized football (including ≥ 3 in college and ≥ 3 seasons in the NFL).
  • Must have played one of following positions offensive lineman, defensive lineman, linebacker, tight end, wide receiver, running back, or defensive back.
  • Agree to provide name and contact information of a study partner who will complete questionnaires regarding subject's mood, behavior, thinking and cognitive function should the subject enroll in the study.

Former Collegiate Football Players

  • English as primary language.
  • No MRI or Lumber Puncture (LP) contraindications.
  • Must have played ≥ 6 years of organized football (with ≥ 3 years at the college level, but no organized football or other contact sport following college).
  • Must have played one of following positions offensive lineman, defensive lineman, linebacker, tight end, wide receiver, running back, or defensive back.
  • No military service.
  • Agree to provide name and contact information of a study partner who will complete questionnaires regarding subject's mood, behavior, thinking and cognitive function should the subject enroll in the study.

Control Group

  • English as primary language.
  • No MRI or Lumber Puncture (LP) contraindications.
  • No history of organized contact sports or known traumatic brain injury (TBI) and/or moderate/severe concussions.
  • No history of participation in any of the following organized sports at any level: football, hockey, rugby, soccer, lacrosse, wrestling, boxing, gymnastics, martial arts, and kickboxing.
  • No military service.
  • Must have BMI ≥ 24.
  • Agree to provide name and contact information of a study partner who will complete questionnaires regarding subject's mood, behavior, thinking and cognitive function should the subject enroll in the study.
  • Must be asymptomatic when screened by telephone.

Exclusion Criteria:

Former NFL and Varsity Collegiate Football Players

  • If they do not meet inclusion criteria.
  • If they have a history of clinical stroke confirmed on neuroimaging.
  • If they have vision or hearing impairment significant enough to compromise neuropsychological testing.
  • If they are unable to undergo MRI/PET Scan.
  • If they are unable to travel to one of 4 study sites to participate.
  • If they cannot provide the name and contact information of an eligible study partner.
  • If they are taking blood thinners that would make LP unsafe.
  • If they do not agree to all study tests and procedures.
  • If they are unable to consent to study procedures.
  • If they have been hospitalized or treated in an emergency room following a severe injury to their head since they stopped playing football (severity determined on phone screening).

Control Group Exclusion:

  • If they do not meet inclusion criteria.
  • If they have vision or hearing impairment significant enough to compromise neuropsychological testing.
  • If they are unable to undergo MRI/PET Scan.
  • If they are unable to travel to one of 4 study sites to participate.
  • If they cannot provide the name and contact information of an eligible study partner.
  • If they report any cognitive concerns or dementia during screening process.
  • If they are unable to consent to study procedures (during eligibility screening and the written consent for study procedures).

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Charles Adler, M.D., Ph.D.

Cerrado para la inscripción

Contact information:

Charles Adler M.D., Ph.D.

(480) 301-8000

cadler@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20253974

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