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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01829256
Other study ID # Pro00044811
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date November 7, 2018

Study information

Verified date February 2019
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diabetic kidney disease (DKD) is associated with high rates of cardiovascular events and death. In addition, DKD is the major cause of end-stage renal disease (ESRD) in the United States. The purpose of this study is to prevent progression of kidney disease among patients with DKD and uncontrolled hypertension (HTN) using a tailored, telehealth intervention that simultaneously address medication management and modifies multiple risk factors through a combination of patient self-monitoring, behavioral therapies and education to optimize adherence and self-efficacy. Additional goals are to improve control of cardiovascular disease risk factors and reduce cardiovascular events and death.

We hypothesize that patients with DKD and uncontrolled HTN who receive this intervention will have less progression, or a smaller decrease in kidney function, after 3 years when compared to the education control group.


Description:

A randomized, controlled trial to slow DKD progression:

1. Using an innovative telehealth approach that is potentially scalable with demonstrable efficacy in reducing antecedents of kidney disease, including poor blood pressure, glucose, and lipid control

2. Enrolling demographically diverse patients from local primary care clinics to allow applicability of our results to the general US population within existing delivery systems; and

3. Targeting patients with moderate DKD (estimated glomerular filtration rate between 45-90 ml/min/1.73m2 with evidence of diabetic nephropathy) and uncontrolled HTN (blood pressure ≥140/90 mm Hg), accounting for about 20% of all patients with diabetes who disproportionately suffer from end-stage renal disease (ESRD), cardiovascular events, and death.


Recruitment information / eligibility

Status Completed
Enrollment 285
Est. completion date November 7, 2018
Est. primary completion date November 7, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- age =18 and less than75 years

- regular use of the Duke University Health System (=2 primary care visits in 3 prior yrs)

- diagnosis of type 2 diabetes

- have at least 2 serum creatinine values available in the 3 prior years, separated by at least 3 months;

- preserved kidney function (eGFR between 45-90 ml/min/1.73m2 on most recent creatinine)

- evidence of diabetic nephropathy

- uncontrolled HTN (1y mean clinic SBP=140 and/or DBP=90).

Exclusion Criteria:

- no access to telephone

- not proficient in English

- nursing home/long-term care facility resident or receiving home health care

- impaired hearing/ speech/ vision

- participating in another trial (pharmaceutical or behavioral)

- planning to leave the area in the next 3 years

- pancreatic insufficiency or diabetes secondary to pancreatitis

- alcohol abuse (>14 alcoholic beverages/ wk)

- diagnosis of non-diabetic kidney disease

- active malignancy (other than non-melanomatous skin cancer)

- life-threatening disease with death probable within 4 years

- Secondary hypertension (renovascular disease, Cushing's syndrome, primary aldosteronism, pheochromocytoma, hypo-/hyperthyroidism, hyperparathyroidism, coarctation of the aorta)

- Pregnancy, Breastfeeding

- Long-term or chronic dialysis

- Dementia

- Renal Transplant

Study Design


Intervention

Behavioral:
Pharmacist telehealth intervention
A tailored intervention with medication management and behavioral components. The behavioral modules may include, diet, exercise, weight, tobacco use, medication management, side effects, diabetes education, DKD/ HTN/ CVD risk and knowledge.Based on the patient's responses to a series of questions, there will be a provision of tailored feedback to reinforce evidence-based behavior for disease and lifestyle management.

Locations

Country Name City State
United States Duke University Health System Clinics Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in kidney function as measured by estimated glomerular filtration rate based on cystatin C(eGFRcys) Measured at Baseline and again at 36 months
Secondary Change in blood pressure, glucose/HbA1c and urine albumin Measured at baseline and again at 36 months
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