- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03279627
Comprehension of Discharge Instructions for Diabetes Therapy and Hospital Readmission
Association of Glycemic Control With Comprehension of Discharge Instructions for Diabetes Therapy and Hospital Readmission
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Background: Diabetes is a major contributor to hospital readmissions and health care expenditures. Previous studies have attempted to identify risk factors for readmission among patients with diabetes. However, no studies have looked at some potentially important factors including duration of diabetes, HbA1c, glycemic excursions preceding hospital discharge, and patient comprehension of discharge instructions provided for home diabetes management. In this study, we propose to examine patient understanding of instructions for insulin therapy provided at the time of hospital discharge as a potential risk factor for readmission during the following 30- and 90-day time periods. In addition, we will examine the contribution of glycemic excursions obtained in the 48-hour period prior to discharge on patient understanding of insulin therapy and risk for readmission.
Purpose: The purpose of this study is to identify and explore the existing components of discharge planning provided to patients with insulin treated diabetes in the inpatient setting and to examine the contribution of glycemic excursions as well as comprehension of discharge instructions among patients with diabetes, in predicting hospital readmissions.
Methods: This will be a prospective non-blinded observational study enrolling non-critically ill, non-pregnant, hospitalized patients aged 18-90 years of age with insulin treated diabetes and no evidence of baseline cognitive. The participants will be recruited from August 2017 to December 2018 from the Inpatient Endocrine and Diabetes Consult Services and from daily reports of patients experiencing BG< 70 mg/dL and >300 mg/dL. Eligible participants will be called within 24-48 hours following hospital discharge at which time they will be asked to complete a Diabetes Management Questionnaire to determine their comprehension of the recommendations provided for home-insulin and other diabetes therapies. This questionnaire will include questions about the types of insulin being used, the doses administered, and times given. Patient interviews will be conducted again via a telephone follow up at approximately 30- and 90-days following discharge with specific questions on home blood glucose control and ER or hospital visits and/or readmissions. The Clinical and Translational Science Institute at the University of Pittsburgh will be consulted for statistical analysis.
Study significance:
This study has the potential to identify modifiable factors that can potentially contribute to the observed frequency of hospital readmissions among patients with insulin treated diabetes. This study could also advocate for discharge protocols and close follow up of patients with insulin-treated diabetes following discharge to ensure appropriate understanding of discharge instructions for insulin therapy and home diabetes management.
Tipo de estudo
Inscrição (Real)
Contactos e Locais
Locais de estudo
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, Estados Unidos, 15213
- University of Pittsburgh Medical Center
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Descrição
Inclusion Criteria:
- Non-pregnant, non-critically ill, hospitalized patients aged 18-90 years with insulin treated diabetes in the hospital
Exclusion Criteria:
- Patients admitted with primary diagnosis of hypoglycemia, DKA; or Hyperglycemic Hyperosmolar Syndrome; patients receiving intravenous narcotic medications; patients discharged to skilled nursing facilities; patients with cognitive impairment defined as dementia or delirium documented in the Electronic Medical Record (EMR); patients with limited life expectancy as determined by "Do Not Resuscitate" Status, or documentation of receiving palliative care or terminal diagnoses with expected survival of less than 1 year
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Modelos de observação: Outro
- Perspectivas de Tempo: Prospectivo
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
|
Hypoglycemia
This group will be those who experience a BG < 70 mg/dl in the 24-48 hour time period preceding hospital discharge.
Study procedures are identical for each group.
All participants in this group will be asked to complete the Diabetes Management Questionnaire.
|
Patients will be asked questions regarding their understanding of instructions for home diabetes management within 48 hours of hospital discharge.
At 1 and 3 months, participants will be contacted to obtain information regarding ER visits or hospital readmissions.
|
|
Hyperglycemia
This group will be those who experience a BG > 250 mg/dl in the 24-48 hour time period preceding hospital discharge.
Study procedures are identical for each group.
All participants in this group will be asked to complete the Diabetes Management Questionnaire.
|
Patients will be asked questions regarding their understanding of instructions for home diabetes management within 48 hours of hospital discharge.
At 1 and 3 months, participants will be contacted to obtain information regarding ER visits or hospital readmissions.
|
|
Glycemic control
This group will be those who maintain BG of 70 to 250 mg /dl in the 24-48 hour time period preceding hospital discharge.
Study procedures are identical for each group, but study outcomes including comprehension of discharge instructions and 1 and 3 month readmissions will be analyzed according to group category.All participants in this group will be asked to complete the Diabetes Management Questionnaire.
|
Patients will be asked questions regarding their understanding of instructions for home diabetes management within 48 hours of hospital discharge.
At 1 and 3 months, participants will be contacted to obtain information regarding ER visits or hospital readmissions.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Patient understanding of discharge instructions for home diabetes therapy according to presence or absence of hypoglycemia (defined as BG < 70 mg/dl), hyperglycemia (defined as BG > 250 mg/dl), or BG 70-250 mg/dl at time of hospital discharge
Prazo: within 48 hours of hospital discharge
|
Participants will be asked to complete a questionnaire regarding their home diabetes medications including timing, adjusting, and medication names.
|
within 48 hours of hospital discharge
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Association between patient understanding of home diabetes therapy and frequency of ER visits and hospital readmissions at 30- and 90-day following the index hospitalization
Prazo: 1 and 3 months following index hospitalization
|
Questionnaire for ER visits and Hospital Readmission
|
1 and 3 months following index hospitalization
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mary T Korytkowski, MD, Univesity of Pittsburgh
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- PRO17050222
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
Ensaios clínicos em Diabetes Management Questionnaire
-
Life Seal Vascular Inc.Auckland City HospitalRecrutamentoAneurisma da aorta abdominalNova Zelândia
-
Shirley Ryan AbilityLabCoapt, LLCAtivo, não recrutandoAmputação de membro inferior abaixo do joelho (lesão) | Amputação de membro inferior acima do joelho (lesão) | Amputação | Dor do membro fantasma | Dor fantasma | Sensação Fantasma | Joelho para Amputação de Membro Inferior | Amputação de membro superior abaixo do cotovelo (lesão) | Dor fantasma após... e outras condiçõesEstados Unidos
-
naomi goldsteinNational Institute of Mental Health (NIMH)Concluído
-
Prof. Dr. Jan LimanUniversity Hospital, Basel, Switzerland; Klinikum Nürnberg; Deutsche ForschungegemeinschaftRecrutamentoAVC hemorrágico intracerebral | AVC Isquêmico Agudo AIS | AVC AgudoSuíça, Alemanha
-
HealthBeacon PlcModena Allergy & AsthmaInscrevendo-se por convite
-
University of California, San FranciscoNational Center for Complementary and Integrative Health (NCCIH); Mount Zion... e outros colaboradoresConcluídoObesidadeEstados Unidos
-
Selcuk UniversityRecrutamento
-
Rema AfifiConcluídoEstresse, Psicológico | Saúde mentalLíbano
-
Mayo ClinicNational Institute on Aging (NIA)ConcluídoTratamento Não Farmacológico da DorEstados Unidos
-
Brigham and Women's HospitalConcluído