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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03839394
Other study ID # Pro00085562
Secondary ID K23HL137611-01A1
Status Completed
Phase N/A
First received
Last updated
Start date October 12, 2020
Est. completion date September 14, 2023

Study information

Verified date November 2023
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to assess the efficacy of a case manager/social worker administered, telephone-based educational curriculum in improving cardiovascular disease related outcomes among HIV-infected clinic patients.


Description:

Fifty high Cardiovascular Disease Risk (CVD) risk clinic patients will be randomized 1:1 to receive either a series of educational pamphlets on CVD risk reduction plus a telephone-based CVD risk reduction curriculum delivered over 24 weeks [intervention arm], or the educational pamphlets alone [control arm]. Anthropomorphic data, blood pressure and lipid profiles will be obtained from patients to assess the efficacy of the intervention in reducing blood pressure and serum low-density lipoprotein levels (LDL).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 14, 2023
Est. primary completion date September 14, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria: - In care at the Duke Infectious Diseases Clinic for HIV and for at least 24 months - On antiretroviral therapy - 2013 American Heart Association 10-year ASCVD risk score = 15%, with a diagnosis of either hypertension or hyperlipidemia - English literate (able to speak and read at a 6th grade level) - Subjects must have the capacity to give legally effective consent. Exclusion Criteria: - Patients with prior diagnosis of acute coronary syndrome, stroke, peripheral vascular disease, and end stage renal disease

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Telephone
A series of educational pamphlets on CVD risk reduction plus a telephone-based CVD risk reduction curriculum will be administered by Clinic-Based Case Managers (CCMs). Six modules will be given over 24 weeks in a rotating fashion on topics relevant to CVD risk. Subjects will be given the pamphlets every 2 weeks corresponding with the first time they receive the telephone - based module.
Other:
Educational pamphlets
A series of 6 handouts will be given to controls once monthly over 6 months on the same topics presented in the telephone modules. Educational packets will be primarily drawn from free printed material available at www.learningaboutdiabetes.org and the American Heart Association website.

Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Duke University National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in ambulatory systolic blood pressure Change of systolic blood pressure will be assessed as an absolute continuous variable, and as a proportion or persons who achieve >5mmHg reduction in systolic blood pressure from baseline baseline, 24 weeks, 48 weeks, 72 weeks
Primary Change in fasting LDL-c levels Assessment of the absolute change in fasting calculated low density lipoprotein cholesterol over the study period. baseline, 24 weeks, 48 weeks, 72 weeks
Secondary Total weight loss Total weight loss from baseline over the study period. baseline, 24 weeks, 48 weeks, 72 weeks
Secondary Change in 10-year atherosclerotic cardiovascular disease (ASCVD) risk score The global cardiovascular disease risk as calculated by the American College of Cardiology/American Heart Association's 10-year risk calculator. baseline, 24 weeks, 48 weeks, 72 weeks
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