A Study of the Impact of Decision Aids to Enhance Shared Decision Making for Diabetes

Overview

Información sobre este estudio

The purpose of this study is to determine the impact of patient decision aids compared to usual care on measures of patient involvement in decision-making, diabetes care processes, medication adherence, glycemic and cardiovascular risk factor control, and use of resources in nonurban practices in the Midwestern United States.

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

  • Primary care provider is participating in trial
  • Adult, ≥ 18 years
  • Has type 2 diabetes
  • English speaking
  • Recognize primary care provider as main diabetes care provider
  • Can state is available for follow-up for six months after treatment decision
  • Specific for diabetes medication
    • Clinical diagnosis of type 2 diabetes for one year or more (c-peptide test is not required)
    • Use 0, 1, or 2 oral hypoglycemic agents at maximum doses
    • Stable but inadequate glycemic control or worsening glycemic control as identified by most recent HbA1c measure over 7.3% within 12 months of the time of eligibility 
    • Identified by provider as a medically-appropriate candidate for diabetes medications, (i.e. no contraindications to taking the medications, e.g., allergy)
  • Specific for cardiovascular medication
    • Clinical diagnosis of type 2 diabetes for any duration (c-peptide test is not required)
    • Identified by provider as a medically-appropriate candidate for statins, (i.e. no contraindications to taking the medications, e.g., allergy)

Exclusion Criteria

  • Major barriers to providing written informed consent and  participating in shared decision making (i.e. severe vision or hearing impairment, cognitive impairment, non-English speaking)
  • Specific for diabetes medication
    • Use insulin therapy
  • Specific for cardiovascular medication
  • Use a statin currently

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Victor Montori, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
.
CLS-20314153

Mayo Clinic Footer