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Activity Monitoring in Patients Undergoing Pain Rehabilitation

Overview

Información sobre este estudio

The primary purpose of this study is to determine if a 3-week interdisciplinary chronic pain self-management program is effective in improving 1) patient-reported measures of pain, function, quality of life mood and sleep; 2) physical capacity; 3) performance as measured by change in activity counts; and 4) sleep efficiency as measured by actigraphy.  Activity and patient reported outcomes as well as measures of performance will all be collected in patients before during and after participation in the 3-week interdisciplinray pain program and subsequently analyzed to determine how much each of these improve over the course of treatment and beyond.

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: 

  • Are between the ages of 18-85 at the time of enrollment in the IPMP.
  • Are scheduled to begin participation in the Pain Rehabilitation Center’s 3-week program for a primary impairment of chronic pain.
  • Are willing to wear an activity monitor for collection of data.
  • Are willing to return for scheduled follow-up research visits.

 

Exclusion Criteria:  

  • Are receiving worker’s compensation.
  • Are unable to provide consent independently/without a LAR.
  • Are pregnant at time of recruitment or become pregnant during the study.
  • Are current employees of Mayo Clinic.
  • Are non-independent ambulators.
  • Have a functional movement disorder.

Eligibility last updated 8/4/22. Questions regarding updates should be directed to the study team contact.

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

Emma Fortune Ngufor, Ph.D.

Comunícate con nosotros para obtener el estatus más reciente

Contact information:

Paul Scholten M.D.

(904) 953-2823

Scholten.Paul@mayo.edu

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Paul Scholten, M.D.

Abierto para la inscripción

Contact information:

Paul Scholten M.D.

(904) 953-2823

Scholten.Paul@mayo.edu

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20523643

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