- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04376112
Influence of Pharmacist and Student Pharmacists on Medication Adherence in Community Pharmacy Setting in Underserved Population
12. april 2022 opdateret af: Loma Linda University
The overall objective is to examine the influence of various services provided by the community pharmacy on patients' diabetes and diabetes-related health outcomes.
Studieoversigt
Status
Trukket tilbage
Intervention / Behandling
Detaljeret beskrivelse
Diabetes affects approximately 30.3 million people in the U.S. and is the 7th leading cause of death (ADA 2019).
Uncontrolled diabetes leads to various complications including cardiovascular disease, kidney disease, diabetic retinopathy, peripheral neuropathy, and lower extremity amputation.
Estimated healthcare expenditure for individuals with diabetes is approximately $327 billion per year (ADA 2017).
In San Bernardino County, the prevalence of diabetes was higher (12.4%) than the national rate (9.4%).
More specifically, the federally qualified health center in which the Loma Linda University (LLU) community pharmacy serves has a diabetes prevalence rate of about 16% (HRSA 2017).
To decrease risk of diabetes complications, HbA1c is recommended to be <7% in most patients; however, about 35% of the investigator's patient population have poorly controlled diabetes which is defined as HbA1c >9% (ADA 2019).
Given high prevalence rates of uncontrolled diabetes in this high-risk population, it is pivotal that individuals are provided with appropriate diabetes self-management strategies, regular monitoring, and preventative care by their primary care provider to adequately control the disease.
Numerous studies illustrate that clinical pharmacists improve health outcomes for chronic disease managements with medication therapy management (MTM) services in underserved patients.
Additionally, team-based or coordinated care with the community pharmacist and the patient's health care providers has also demonstrated to assist with improvements in clinic outcomes of chronic diseases.
Recently, combination of blister packaging and MTM services have been shown to improve medication adherence and clinical endpoints.
Given the high prevalence of diabetes in this community, there is a critical need to achieve improvement in clinical diabetes outcomes possibly via monthly blister packaging and MTM services including point-of-care testing (POCT).
Undersøgelsestype
Interventionel
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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California
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San Bernardino, California, Forenede Stater, 92410
- Loma Linda University Pharmacy at SACHS
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- ≥18 years of age, any gender
- Hemoglobin A1c >8.5%
- Taking total of ≥5 medications and taking ≥2 anti-diabetes medications
Exclusion Criteria:
- Unable to give informed consent
- Individuals included in Inland Empire Health Plan's Complex Care Program
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Faktoriel opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Standard for pleje
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None.
Regular visits to primary care physician.
Will measure HbA1c and blood pressure at baseline, 3, and 6 months
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Eksperimentel: Pharmacist Intervention
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These participants will be randomized into one of the following two cohorts: standard of care (SOC) and pharmacy intervention group (blister packaging + MTM services).
For pharmacy intervention (PI) group, the POCT will be used to measure HbA1c and blood pressure (BP) at baseline, 3, and 6 months during medication therapy management (MTM) service.
Recommendation from MTM services will be documented in the patients' electronic medical records (EMRs) and shared with their primary care providers.
For the SOC group, HbA1c and BP will be measured at the physician's office and researchers will have an access to participants' EMR.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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hemoglobin A1c
Tidsramme: Change between baseline and 6 months
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Finger prick for HgA1c at baseline and at 6 months.
Goal < 7% normal above 7% is abnormal
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Change between baseline and 6 months
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blood pressure
Tidsramme: Change between baseline and 6 months
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Blood pressure will be checked at baseline and at 6 months.
Goal BP is 130/80 mmHg and above 130/80 mmHg is abnormal.
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Change between baseline and 6 months
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Medication adherence
Tidsramme: Change between baseline and 6 months
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Adherence of medication will be determined by patients picking up their medications.
Patient profile will track every insurance claims for the medications.
The proportion of days covered indicates the medication adherence, and it will be calculated at the end of 6 months.
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Change between baseline and 6 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Forventet)
1. oktober 2020
Primær færdiggørelse (Faktiske)
1. januar 2021
Studieafslutning (Faktiske)
1. januar 2021
Datoer for studieregistrering
Først indsendt
23. september 2019
Først indsendt, der opfyldte QC-kriterier
4. maj 2020
Først opslået (Faktiske)
6. maj 2020
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. april 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. april 2022
Sidst verificeret
1. april 2022
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 5190360
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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