- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03114592
Understanding the Role of Patient Behavior Change in Improving AKI Outcomes (Change AKI)
Understanding the Role of Patient Behavior Change in Improving AKI Outcomes (Change AKI Study)
Studieöversikt
Detaljerad beskrivning
Acute kidney injury (AKI) is an increasingly common complication of acute hospitalizations. Hospital-related AKI, commonly caused by hemodynamic changes or contrast exposure, carries a threat of adverse outcomes that persists following hospital discharge, with an independent and graded association with long-term mortality. It is estimated that, approximately 13% of individuals with acute coronary syndrome (ACS) will develop some degree of AKI during their hospitalization. Survivors of AKI consume significantly greater health resources than the general population, and suffer exceedingly poor renal outcomes, including persistent loss of kidney function, progression to end stage renal disease (ESRD), and increased risk of recurrent AKI. It is estimated that 25% of individuals with an AKI-related hospitalization will be readmitted with recurrent AKI within 12 months of discharge, highlighting a critical need to address ongoing AKI risk once the acute hospitalization is complete. Patient-centered educational interventions that intensify awareness of potentially hazardous situations may reduce AKI recurrence. For example, commonly prescribed therapies such as diuretics or ACE inhibitors may threaten the renal safety of individuals at high risk of recurrent AKI if taken when significantly volume deplete, such as during an acute gastroenteritis, and in most cases should be held until one can eat and drink normally; Nonsteroidal Anti-inflammatory Drugs (NSAIDs) may exacerbate AKI risk if taken in combination with diuretics or ACE inhibitors even when volume replete and should be completely avoided. Tailored educational curricula surrounding these and other topics pertinent to AKI survivors may reduce recurrent hospitalizations and lower healthcare costs. In the absence of a patient centered outpatient approach to AKI education, the development of effective and sustainable AKI prevention strategies remains unlikely.
Our long-term goal is to develop patient-centered educational materials to reduce AKI recurrence. We hypothesize that a tailored educational curriculum will improve patient awareness of potential hazards and reduce AKI recurrence among hospital-based AKI survivors. Therefore, our overall objective for this proposal is to pilot test and evaluate the feasibility of a patient-centered mobile health (mHealth) educational curriculum for hospitalized AKI survivors at Duke Medical Center.
Aim 1: To test the feasibility and acceptance of a mHealth patient safety curriculum in hospitalized AKI survivors.
Hypothesis 1: Patient safety risk awareness at 1 month will be higher in the educational intervention arm than the usual care arm.
Aim 2: To determine if a mHealth educational curriculum improves patient safety behaviors in AKI survivors.
Hypothesis 2: High-risk safety behaviors will be reduced at 1 month in AKI survivors receiving the educational intervention, but not in the usual care arm.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
North Carolina
-
Durham, North Carolina, Förenta staterna, 27710
- Duke University Hospital
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Diagnosis of acute kidney injury as diagnosed by renal care team
- On medical or surgical services
- Over 18 year of age
- Ability to read and speak English
Exclusion Criteria:
- Legal blindness or deafness
- Pregnant
- Cognitive impairment that limits ability to consent
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Inget ingripande: Standard Care
|
|
|
Experimentell: mHealth Tool
|
The curriculum in the mHealth tool was derived in consultation with patient safety, informatics and adult educational curricula experts, and is comprised of clinical vignettes describing the post-hospital discharge stories of two hypothetical AKI survivors.
opics of emphasis included NSAID risk awareness and avoidance of volume depletion when ill ("Sick Day Protocol").
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in Patient Safety-Related Knowledge (Patient safety risk awareness)
Tidsram: Baseline, 1 month
|
mHealth tool and how knowledge changes pre/post intervention
|
Baseline, 1 month
|
|
Change in Patient Safety Behavior and Risk awareness
Tidsram: Baseline, 1 month
|
Survey assessing patient safety behavior and risk awareness
|
Baseline, 1 month
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
User Satisfaction
Tidsram: 5 minutes
|
Satisfaction of mHealth tool
|
5 minutes
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Clarissa J Diamantidis, MD, Duke University
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- Pro00080287
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-planbeskrivning
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
Kliniska prövningar på Akut njurskada
-
Chung Shan Medical UniversityNational Science and Technology Council, TaiwanHar inte rekryterat ännuFetma typ 2 diabetes mellitus | Metabolisk dysfunktion-associerad Steatotisk leversjukdom | Kardiovaskulär-kidney-metaboliskt syndromTaiwan
-
CHU de ReimsHar inte rekryterat ännuFluid Responsivity in Early Post-Kidney Transplantation PeriodFrankrike
-
Ahmed Hamed Kassem AbdelaalAvslutadUtvärdering av giltigheten av thoracolumbar AO Spine Injury Score (TL AOSS) i A3- och A4 -frakturerEgypten
-
University Hospital, Basel, SwitzerlandHar inte rekryterat ännuKardiovaskulär-kidney-metaboliskt syndrom | Cradiovaskular-kidney-lever-metabolisk (CKLM) -syndromSchweiz
-
Camille N. Kotton, MDKamada, Ltd.; University of Texas Southwestern Medical CenterRekryteringCytomegalovirus | Njurtransplantation; Komplikationer | Organtransplantation | Levertransplantationskomplikationer | Samtidig lever-Kidney-transplantation; KomplikationerFörenta staterna
-
Hospital Universitari Son DuretaEspen; This research prize was funded by Nestle Nutrition Institute and...AvslutadMåttligt till allvarligt trauma, enligt definitionen av en | Injury Severity Score (ISS) > 12 poäng inkluderades i studien.Spanien
-
SanionaAvslutadHypothalamic Injury-induced Obesity (HIO)Danmark
-
Children's Oncology GroupRekryteringSteg I Mixed Celltype Kidney Wilms tumör | Steg II Mixed Cell Type Kidney Wilms tumör | Steg III blandad celltyp njurar Wilms tumör | Steg IV Mixed Cell Type Kidney Wilms tumörFörenta staterna, Kanada, Australien
-
Nanjing Medical UniversityHar inte rekryterat ännuKardiovaskulär-kidney-metaboliskt syndrom
-
houyajingAnmälan via inbjudanSialorhea True Bulbar Pares Medullary InjuryKina
Kliniska prövningar på mHealth tool
-
University of California, DavisNational Institute of Mental Health (NIMH); Washington University School... och andra samarbetspartnersAnmälan via inbjudanFörsta episod psykos (FEP)Förenta staterna
-
Liverpool John Moores UniversityLiverpool Heart and Chest Hospital NHS Foundation Trust; University Hospitals... och andra samarbetspartnersAvslutad
-
NYU Langone HealthWeizmann Institute of Science; American Heart AssociationAvslutadÖvervikt och fetma | Pre-diabetesFörenta staterna
-
The Hospital for Sick ChildrenUniversity Health Network, Toronto; Trillium Health PartnersAvslutadDiabetes mellitus, typ 1Kanada
-
University of WashingtonRekrytering
-
Kaiser PermanenteUniversity of California, San Francisco; OCHIN, Inc.AvslutadHypertoni | Diabetes mellitus, typ 2Förenta staterna
-
Pain ConcernThe Thistle Foundation; Health and Social Care Alliance Scotland (the ALLIANCE) och andra samarbetspartnersAvslutadKronisk smärta | Kroniskt smärtsyndrom | Kronisk smärta, utbredd | Kronisk smärta på grund av trauma | Kronisk smärta på grund av malignitet (fynd) | Kronisk smärta på grund av skada | Kronisk smärta efter proceduren | Kronisk smärta höftStorbritannien
-
Thomas Jefferson UniversityAvslutadHematopoetisk och lymfoid cellneoplasma | Malign fast neoplasmaFörenta staterna
-
The Hong Kong Polytechnic UniversityAvslutad
-
University of WolverhamptonThe Royal Wolverhampton Hospitals NHS TrustRekryteringAvancerat prostatacancerStorbritannien