- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03207646
Smartphone GUIded MeDication AdherencE and Rehabilitation in Patients With Coronary Artery Disease (smartGUIDE)
Smartphone GUIded MeDication AdherencE and Rehabilitation in Patients With Coronary Artery Disease (smartGUIDE)
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
California
-
Stanford, California, Forente stater, 94305
- Stanford Healthcare
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion criteria:
I. ≥ 18 years of age
II. Patient at Stanford Health Care with evidence of CAD (atherosclerosis of one or more coronary arteries or clinical evidence or documentation of ischemia, infarction) OR a diagnosis related to CAD (i.e. ischemic heart disease ICD-10-Code: I20-25).
III. Prescription of a P2Y12 antagonist and/or a statin for an anticipated duration of at least 3 months following discharge
IV. Possession of a compatible (iPhone 5s or later; OS 8.1 or higher) smartphone with an active phone number and data plan. The smartphone must be in continued possession of the participant. It may not be a shared device and must exclusively remain in the possession of the participant during the study period. The smartphone must have an active cellular phone number and cellular data subscription. Wi-Fi internet capability is not a substitute for an active cellular data plan.
V. Must sign an informed consent form (ICF) indicating that he or she understands the purpose of, and procedures required for, the study and is willing to participate in the study.
VI. Willing to have the mobile application installed on a smartphone and use it every day during the entire study period VII. Willing to provide oral confirmation indicating that he/she is currently not using a medication adherence application.
VIII. Ability to read and understand English.
Exclusion criteria:
Any potential participant who meets any of the following criteria will be excluded from participating in the study:
I. Anticipated inability to adhere to the mobile application (BrightHeart®) based on opinion of site Principal Investigator (PI).
II. Current use of adherence tracking devices, electronic, smartphone or computer applications, including but not limited to smart pill bottles, pill timers, radiofrequency tagged medications or dispensers, mobile applications, or automated phone reminders. Pill organizers that remind participants when to take medicine with beeps or alerts are exclusion.
a. Note: Pharmacy and health care plan automated refill reminders are permitted and are not exclusion. Pill organizers or containers that only compartmentalize a participant's medications based on days of the week are not exclusion.
III. Cognitive, visual, hearing, voice, or motor impairment that would prevent completion of study procedures or use of mobile phone. Co-morbidities that would preclude participation (e.g. ongoing chemotherapy) or planned hospitalization for complex procedures as determined by the PI (e.g. bypass, valve or aortic surgery, transarterial valve replacement) IV. End-stage of one of the following: heart failure (using left ventricular assist device or listed for heart transplantation), renal disease, lung disease, liver disease.
V. Any condition with a life expectancy less than 3 months. VI. Employee of the investigator or study site, with direct involvement in the proposed study or other studies under the direction of that investigator or study site, as well as family members of the employees or the investigator VII. Any other condition as determined by the PI.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: smartphone-based cardiac rehabilitation
The BrightHeart® mobile application is installed on the smartphone and a heart coach set up and guides the participant through a cardiac care program.
|
BrightHeart® has two components: smartphone mobile based application and a human coach.
It is a combined approach of medication adherence, exercise, diet, sleep and stress reduction.
|
Ingen inngripen: Control
Standard-of-care alone.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Medication adherence
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
The proportion of days coverd (PDC) expressed as a percentage but considered as a continuous variable of the composite of the prescribed P2Y12 receptor antagonist and/or the statin.
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Medication adherence II
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Proportion of participants with PDC ≥ 80% of the composite of the P2Y12 receptor antagonist and/or the statin
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Medication adherence III
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
The PDC of each medication of the composite
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Medication adherence IV
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Proportion of participants with PDC ≥ 80% of each of the composite
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Medication adherence V
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Mean time from discharge to first fill
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Medication persistence
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
proportion of patients with an active prescription at three months of a statin and P2Y12 inhibitor
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors I
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Serum LDL-C at End of Study
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors II
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Proportion of participants within target blood pressure (<140/90 mmHg or <130/80 mmHg for patients with diabetes mellitus or chronic kidney disease) at End of Study
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors III
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Proportion of participants with HbA1c ≤ 7% at End of Study (only if diabetes mellitus was known at time of inclusion)
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors IV
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Change in body weight from baseline to End of Study
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors V
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Change in quality of life (measured by EQ-5D-3L14) from day 3-10 after discharge to End of Study
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors VI
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Change in patient activation (measured by PAM®1015) from day 3-10 after discharge to End of Study
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Cardiovascular risk factors VII
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Physical activity at End of Study (measured by a physical acitivity questionnaire)
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Exploratory I: Rehospitalization
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
30-day rehospitalization for any reason
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Exploratory II: Cardiovascular outcomes
Tidsramme: Baseline through End of Study visit - approximately 90 days per participant.
|
Major adverse cardiac events (MACE) defined as: Death, myocardial infarction, acute coronary syndrome, out of hospital cardiac arrest, stent thrombosis, repeat revascularization at 90 days
|
Baseline through End of Study visit - approximately 90 days per participant.
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Minang (Mintu) Turakhia, MD, Stanford University
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 39555
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
produkt produsert i og eksportert fra USA
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
Kliniske studier på Koronararteriesykdom
-
IRCCS Policlinico S. DonatoRekrutteringAnomalous aortic origin of the coronary artery (AAOCA)Italia
-
Medtronic CardiovascularFullførtArteriosclerosis of coronary artery bypass graftCanada, Forente stater
-
Lawson Health Research InstituteFullførtArteriosclerosis of arterial coronary artery bypass graftCanada
-
Deutsches Herzzentrum MuenchenFullførtArteriosclerosis of arterial coronary artery bypass graftTyskland
-
William Beaumont HospitalsFullførtKoronararteriesykdom | Arteriosclerosis of coronary artery bypass graftForente stater
-
Izmir Bakircay UniversityFullførtMyocardial Bridge of Coronary ArteryTyrkia
-
ITAB - Institute for Advanced Biomedical TechnologiesAzienda Ospedaliero, Universitaria Ospedali RiunitiFullførtMyocardial Bridge of Coronary ArteryItalia
-
University Hospital OstravaRekrutteringIn-Stent Carotis Artery RestenosisTsjekkia
-
Sohag UniversityHar ikke rekruttert ennåUmblical artery Doppler under termin graviditetEgypt
-
Baylor College of MedicineFullførtLungeblødning | MAPCA - Major Aortopulmonary Collateral ArteryForente stater
Kliniske studier på BrightHeart®
-
Galderma R&DFullført
-
Dong-A ST Co., Ltd.FullførtFunksjonell dyspepsiKorea, Republikken
-
Chong Kun Dang PharmaceuticalFullført
-
Amir AzarpazhoohInstitut Straumann AGFullført
-
Novartis PharmaceuticalsFullførtLungesykdom, kronisk obstruktiv (KOLS)Argentina
-
GuerbetFullførtPrimær hjernesvulstColombia, Korea, Republikken, Forente stater, Mexico
-
Chung-Ang University Hosptial, Chung-Ang University...UkjentFunksjonell dyspepsiKorea, Republikken
-
Sanofi Pasteur, a Sanofi CompanyFullførtPertussis | Difteri | PolioForente stater
-
Sanofi Pasteur, a Sanofi CompanyFullførtPertussisForente stater