- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03442595
MedStar Diabetes Pathway Chart Reviews (MedstarBC2)
Expanded MedStar Diabetes Pathway Ongoing Chart Review Protocol
연구 개요
상세 설명
The MedStar Diabetes Pathway (MDP) early pilot program has generated evidence that an innovative technology-enabled "Boot Camp" approach to the delivery of diabetes survival skills education and medication management has a significant impact on glycemic control and healthcare utilization measures. The MDP is a 12 week Diabetes "Boot Camp" technology-enabled intervention which will offer learner-centered survival skills self-management education (DSSE) and algorithm-driven diabetes medications (DM) titration by Endocrinologist-supervised Certified Diabetes Educators (CDE), NPs and PharmDs. The program has been offered at 5 MedStar Medical Group (MMG) Primary Care Practices from November 2014 to February 2016 to high risk adults with uncontrolled type 2 diabetes who have a hemoglobin A1C (A1C) level -a marker of average blood glucose (BG) levels in the 2-3 months prior to the time the test is done- which is at or above 9% - considered to be poor control, and 1 or more additional risk factors for poor health outcomes. The program has been well received by MedStar Primary Care Providers and their diabetes patients. Patients that participated in the MDP achieved significantly higher A1C reduction and decreased risk risk for acute care utilization then matched controls that received standard of care. The pilot evidence demonstrated a significant impact on glycemic control and healthcare utilization measures as the result of a concise, focused DM education and medication management intervention. Building on the success of the MDP Phase 1.0 pilot, the next steps in expanding the program will be as follows:
- Transition of the Pathway from early feasibility pilot to the next phase as an expanded pilot program integrated within the MedStar Health System care delivery network and built upon a sustainable infrastructure across early adopter MMG practice sites.
- Expand recruitment to include high risk patients with uncontrolled type 2 diabetes, including those with a new diagnosis and A1C >9%, who have MedStar Emergency Department and/or Inpatient encounters
- Spread to additional targeted MedStar Primary Care Practices and/or to MedStar Managed Care Plan participants.
Chart reviews and data collection during the expansion phase will be essential to guide the process and allow rapid cycle adjustments to maximize the impact of the program and utilization of resources for the benefit of our patients.
연구 유형
등록 (실제)
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Diagnosis of Type 2 Diabetes, A1C equal or higher than 9%, active patient of medstar health provider, english speaking, willing and able to participate in the program
Exclusion Criteria:
- A1C less than 9%, severe illness that precludes participation such severe congestive heart failure or COPD, advanced kidney disease, recent acute illness such as heart attack or stroke in the past 30 days, active cancer, severe mental illness, high dose steroid, other types of diabetes, pregnant or lactating.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
Cases
patients with uncontrolled type 2 diabetes mellitus that participate in the MedStar Diabetes Pathway
|
Patients receive intensive knowledge based diabetes education and algorithm driven medication management over a period of 12 weeks.
|
|
Matched controls
patients with uncontrolled type 2 diabetes that match the cases on 5 criteria and received standard of care diabetes management with a MedStar provider
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Percent Change in A1C
기간: 12-16 weeks
|
Change in Hemoglobin A1C from baseline to 12-16 weeks for both cases and controls
|
12-16 weeks
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Risk for Emergency Room Visits at 30 Days From Baseline as Measured by Incidence Risk Ratio
기간: 30 days
|
Comparison of risk of incurring an emergency room visits at 30 days from baseline for cases and controls.
This was done by calculating and comparing the incidence risk ratio for an ER visit for each group and comparing them.
|
30 days
|
|
Risk for Hospitalizations at 30 Days From Baseline
기간: 30 days
|
Comparison of risk for experiencing a hospital visit within 30 days from baseline in both group.
This was done by calculating the incidence risk ratio for hospitalizations for cases and controls at 30 days from baseline and comparing them.
|
30 days
|
|
Risk for Composite of Emergency Room Visits and Hospitalizations at 30 Days From Baseline
기간: 30 days
|
Comparison for risk of experiencing a visit to the emergency room and/or the hospital at 30 days from baseline.
This was measured by calculating the Incidence risk ratio for acute care utilization at 30 days from baseline for both cases and controls and comparing them.
|
30 days
|
|
Risk for Emergency Room Visits at 90 Days From Baseline
기간: 90 days
|
Comparison of the risk of experiencing an emergency room visit at 90 days from baseline in both groups.
This was done by calculating the Incidence risk ratio for an emergency room visit at 90 days for both cases and controls and comparing them
|
90 days
|
|
Risk for Hospitalizations at 90 Days From Baseline
기간: 90 days
|
Comparison of the risk for experiencing a hospitalization within 90 days from baseline in both groups.
This was done by calculating the Incidence Risk Ratio for hospitalizations for cases and controls within 90 days of baseline and comparing them.
|
90 days
|
|
Composite of Risk for Hospitalizations and Emergency Room Visits Within 90 Days From Baseline
기간: 90 days
|
Comparison of the risk for experiencing a hospitalization and/or emergency room visit within 90 days from baseline for both groups.
This was done by calculating then comparing the incidence risk ratio for acute care utilization within 90 days from baseline for cases and controls.
|
90 days
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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