Resting State Connectivity in Adolescents with Postural Orthostatic Tachycardia Syndrome and Chronic Pain

Overview

Información sobre este estudio

The purposes of this study are to compare the functional connectivity in adolescent patients with Postural Orthostatic Tachycardia Syndrome (POTS) both with and without chronic pain, to those with chronic pain alone, to that of healthy controls; to evaluate whether there is a change in functional connectivity following participation in an intensive rehabilitation-oriented program previously demonstrated to have excellent outcomes with regard to functional recovery and symptom control; and to correlate outcomes using standardized symptom and function rating scales to imaging findings.

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:  Group # 1 (ONLY POTS):

  • Adolescents between ages of 13 and 18 years.
  • Patients will complete the three week Pediatric Pain Rehabilitation Center program.
  • POTS will be identified on the basis of accepted criteria (chronic symptoms of orthostatic intolerance, with heart rate increase of greater than 40 beats per minute or more with head up tilt, in the absence of orthostatic hypotension).
  • For this study, the diagnosis will have been made on the basis of autonomic reflex screening performed at Mayo Clinic.
  • No-Chronic pain. Chronic pain is identified as pain lasting more than 12 weeks; at the point of referral to the PPRC, pain is identified as causing functional impairment. 
  • Patients will have the ability to assent for the participation in the research study.

Exclusion Criteria: 

  • Documented disability including developmental delay, cognitive disability, blindness, deafness, paralysis, or psychosis.
  • Metal implants, such as pacemakers or braces
  • Women cannot be pregnant or breastfeeding.
  • Patients will be excluded if they do not complete the three week PPRC program.

Inclusion Criteria: Group # 2 (POTS and Chronic Pain):

  • Adolescents between ages of 13 and 18 years.
  • Patients will complete the three week Pediatric Pain Rehabilitation Center program.
  • POTS will be identified on the basis of accepted criteria (chronic symptoms of orthostatic intolerance, with heart rate increase of greater than 40 beats per minute or more with head up tilt, in the absence of orthostatic hypotension). For this study, the diagnosis will have been made on the basis of autonomic reflex screening performed at Mayo Clinic.
  • Chronic pain is identified as pain lasting more than 12 weeks; at the point of referral to the PPRC, pain is identified as causing functional impairment. 
  • Patients will have the ability to assent for the participation in the research study.

Exclusion Criteria: 

  • Documented disability including developmental delay, cognitive disability, blindness, deafness, paralysis, or psychosis.
  • Metal implants, such as pacemakers or braces
  • Women cannot be pregnant or breastfeeding.
  • Patients will be excluded if they do not complete the three week PPRC program.

Inclusion Criteria: Group # 3 (Chronic Pain Alone):

  • Adolescents between ages of 13 and 18 years.
  • Patients will complete the three week Pediatric Pain Rehabilitation center Program
  • No POTS diagnosis.
  • Chronic pain is identified as pain lasting more than 12 weeks at the point of referral to the PPRC; pain is identified as causing functional impairment.
  • Patients will have the ability to assent for the participation in the research study.

Exclusion Criteria: 

  • Documented disability including developmental delay, cognitive disability, blindness, deafness, paralysis, or psychosis.
  • Metal implants, such as pacemakers or braces.
  • Women cannot be pregnant or breastfeeding.
  • Patients will be excluded if they do not complete the three week pediatric Pain Rehabilitation Center Program.

Inclusion Criteria: Control Group

  • Adolescents between ages of 13 and 18 years.
  • Patients will have the ability to assent for the participation in the research study.

Exclusion Criteria:

  • Documented disability including developmental delay, cognitive disability, blindness, deafness, paralysis, or psychosis.
  • Metal implants, such as pacemakers or braces.
  • Women cannot be pregnant or breastfeeding.
  • Any active acute or chronic medical condition.

Inclusion Criteria: Parent Group

  • Be a parent or legal guardian of a recruited participant for this study.
  • Be able to provide informed consent to participate.

Exclusion Criteria:

  • Documented disability including developmental delay, cognitive disability, blindness, deafness, paralysis, or psychosis.

 

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Kelsey Klaas, M.D.

Abierto para la inscripción

Contact information:

Brandi Johnson

(507) 293-9555

Johnson.Brandi1@mayo.edu

More information

Publicaciones

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CLS-20485247

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