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临床试验/NCT03334370
NCT03334370已完成不适用

Evaluation of Quality of Care - Shared-Care Programme, HA

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 620 人开始时间: 2010年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
620
试验地点
1
主要终点
Change of the proportion of patients who have achieved a HbA1c <7.5%.

研究概览

简要总结

Diabetes mellitus (DM) and hypertension (HT) are major causes of morbidity and among the top 10 causes of deaths in Hong Kong in 2008 (Department of Health 2009). The Hospital Authority (HA) has initiated service improvement through introducing the shared-care (SC) programme to improve the quality of care (QOC) for DM and HT patients. The evaluation on the QOC is an essential part of the programme in order to inform future policy. The Family Medicine Unit (FMU) of the University of Hong Kong (HKU) has been appointed by the HA to carry out the evaluation of the QOC of the programme.

The Action Learning and Audit Spiral methodologies to measure whether the target standard of care intended by the SC programme is achieved. Each SC participating clinic and private medical practitioner (PMP) will be invited to complete a structured evaluation questionnaire. The data of all patients who have enrolled into the programme will be included in the evaluation on the process and outcomes of care. A hundred and thirty participants will be followed up by telephone to evaluate the effect of the programme in quality of life (QOL), patient enablement, and global rating of change in health condition at baseline and 6 months after enrolment. Data on the process of care will be retrieved from the HA medical records.

Main Outcome Measures: The primary outcomes are the proportion of participants who received the criterion process of care and achieved a HbA1c level <7.5%.

Data Analysis: Descriptive statistics on proportions of clinics or subjects meeting the quality of care criteria will be calculated. The outcomes of SC patients will be compared at 6, 12, 24, 36 and 48 months by paired sample t-test. The outcomes between SC patients and control group will be compared by independent sample t-test or Chi-square test.

Hypothesis: The QOC of the SC programme will be determined. Areas of deficiency and possible areas for quality enhancement will be identified. The results of this study will provide empirical evidence on whether the HA's SC programme can achieve equivalent QOC as the usual HA care for diabetes mellitus (DM) patients. The information will be used to guide service planning and policy decision making.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with diabetes mellitus who have received care at the specialist outpatient clinic (SOPC)for at least 2 years, stratified to be of low risk and have normal renal function as defined by the plasma creatinine level.

排除标准

  • Patients will be excluded if they are stratified to be at high cardiovascular risk or are suffering end stage renal failure, on dialysis or after transplantation, or on insulin, or do not give consent to be transferred.

结局指标

主要结局

Change of the proportion of patients who have achieved a HbA1c <7.5%.

时间窗: June, 2011; December, 2011; December, 2012; December, 2013; December, 2014

Change of the proportion of clinics that have satisfied each of the structure criteria.

时间窗: December, 2010; December, 2011; December, 2012; December, 2013; December, 2014

Change of the proportion of patients who have received with the SC criterion process of care.

时间窗: June, 2011; December, 2011; December, 2012; December, 2013; December, 2014

次要结局

  • Blood pressure (BP)(Baseline, 6, 12, 24, 36 and 48 months after enrollment.)
  • Patient reported outcomes (PRO) measured by the change in the Global Rating Scale (GRS) at 6 months.(Baseline and 6 months after the first administration of questionnaire.)
  • Service utilization outcomes measured by hospital attendance rates at baseline and 12, 24, 36 and 48 months after enrollment.(Baseline, 12, 24, 36 and 48 months after enrollment)
  • Low-density lipoprotein (LDL)(Baseline, 6, 12, 24, 36 and 48 months after enrollment.)
  • Patient reported outcomes (PRO) measured by the change in Short Form-12 version 2 (SF-12v2) scores at 6 months.(Baseline and 6 months after the first administration of questionnaire.)
  • Service utilization outcomes measured by accident & emergency (A&E) attendance rates at baseline and 12, 24, 36 and 48 months after enrollment.(Baseline, 12, 24, 36 and 48 months after enrollment)
  • Cardiovascular complications(Baseline, 6, 12, 24, 36 and 48 months after enrollment.)
  • Service utilization outcomes measured by General Outpatient Clinics (GOPC) attendance rates at baseline and 12, 24, 36 and 48 months after enrollment.(Baseline, 12, 24, 36 and 48 months after enrollment)
  • Patient reported outcomes (PRO) measured by the change in the Patient Enablement Instrument (PEI) scores at 6 months.(Baseline and 6 months after the first administration of questionnaire.)
  • Body mass index (BMI)(Baseline, 6, 12, 24, 36 and 48 months after enrollment.)
  • Service utilization outcomes measured by specialist outpatient clinic (SOPC) attendance rates at baseline and 12, 24, 36 and 48 months after enrollment.(Baseline, 12, 24, 36 and 48 months after enrollment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Cindy L.K. Lam

Clinical Professor

The University of Hong Kong

研究点 (1)

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