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Nurse Case Management to Improve Hepatitis C Care in HIV Co-infection

Nurse Case Management to Improve Linkage to Hepatitis C Care and Treatment Initiation in HIV Co-infection: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02707991
Acronym
Care2Cure
Enrollment
68
Registered
2016-03-15
Start date
2016-07-31
Completion date
2018-08-31
Last updated
2019-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis C, Chronic, HIV

Keywords

Continuity of Patient Care, Treatment Cascade

Brief summary

Effective all-oral medications are finally available to cure hepatitis C virus, which affects more than 4 million Americans and one-in-four people living with HIV. However, many barriers exist that prevent people with HIV/HCV co-infection from getting this curative treatment, including low knowledge, competing demands, and drug interactions with HIV medications. This study evaluates if a hepatitis C nurse case management intervention in an HIV primary care clinic will improve patient attendance to hepatitis C care and help people start hepatitis C treatment earlier. Half of the participants will receive brief case management with a nurse, while the other half will receive usual clinic care.

Detailed description

Hepatitis C virus (HCV) is a leading cause of liver cancer and HCV-related liver disease is among the most common causes of non-AIDS related death among people living with HIV (PLWH). One quarter of PLWH in the U.S. are co-infected with HCV, which leads to a 3-fold increase in progression to end stage liver disease and liver cancer. HCV can be cured, but less than half of PLWH with chronic HCV in the U.S. have linked to HCV care, and about 7% initiated treatment. Poor treatment initiation rates historically have been due to low efficacy among PLWH, but HCV care now is at a turning point. The investigators have the ability to substantially decrease HCV-related morbidity and mortality in PLWH with the availability of effective all-oral treatment. As patients are funneled into HCV care, improving the process of linkage to care and treatment preparation related to HIV medication modifications necessary for current HCV regimens is essential to maximize the lifesaving potential of available therapies among PLWH. There are several barriers to linkage to HCV care and treatment. HCV is a silent epidemic often presenting no symptoms for 20 years. Knowledge about HCV and its available therapies is also low and lags behind new advancements in HCV treatment. Competing work, school and caregiving demands has also historically led to low motivation to engage in HCV care. For PLWH who are linked to HCV care, drug interactions between new HCV therapies and HIV treatment regimens introduce a new barrier to HCV treatment initiation. Up to 88% of PLWH will need to switch their HIV treatment regimen to avoid contraindicated drug interactions. The April 8, 2015 Guidelines for the Use of Antiretroviral Agents in HIV-1-infected Adults and Adolescents emphasize the need to modify HIV regimens to treat HCV in many PLWH. But modifying HIV treatment regimens can have severe negative consequences, including decreased quality of life, increased symptom burden, and loss of viral suppression. Interventions that both increase HCV knowledge and support HIV treatment modifications in the setting of drug interactions are needed to improve linkage to HCV care and decrease time to treatment initiation. In similar settings and populations, nurse case management interventions have been shown to improve these outcomes. However, few of these interventions have been rigorously tested in the context of HCV. This study is a randomized, single-blinded controlled trial to test whether a nurse case management intervention will improve the HCV treatment cascade among PLWH in an HIV primary care setting compared to usual care. Specifically, this study aims to: 1. Test whether a nurse case management intervention will increase linkage to the Viral Hepatitis Clinic among persons with HIV/HCV co-infection compared to usual care; Hypothesis: A higher proportion of those who are randomized to the intervention arm will attend the Viral Hepatitis Clinic within 60 days of randomization compared to those who receive usual care. 2. Determine if a nurse case management intervention will decrease time to HCV treatment initiation among persons with HIV/HCV co-infection compared to usual care; Hypothesis: Those who are randomized to the intervention arm will have a decreased time to HCV treatment initiation from the point of randomization compared to those who receive usual care. 3. Describe the characteristics associated with uptake of HCV care among people living with HIV, controlling for covariates; Research question 2.1: What patient-level characteristics are associated with increased uptake of HCV care?; Research question 2.2: Compared to the known historical barriers to engaging in HCV care, what factors continue to be associated with uptake of HCV care in the new paradigm of HCV treatment for people living with HIV?

Interventions

Participants will receive one baseline nurse case management study visit in addition to appointment reminders one week and one day before the scheduled hepatitis clinic appointment. Those who link to the Viral Hepatitis Clinic and are identified as eligible to start hepatitis C therapy by their health care provider will have one additional study visit with the nurse case manager to coordinate drug-drug interaction prevention.

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* HIV infection * Chronic hepatitis C infection * Did not attend a hepatitis C specialty appointment in the past year * Able to speak English * Current patient at the John G. Bartlett Specialty Practice at Johns Hopkins Hospital (at least 1 visit in the past year)

Exclusion criteria

* Pregnancy * Emergency medical care needed * Unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Linked to Care60 daysThis will be assessed based on the number of participants who attend an appointment at the Viral Hepatitis Clinic within 60 days of enrolling in the study. A participant is considered linked to care if he/she attends an appointment at the clinic. A participant is considered not linked to care if he/she does not attend an appointment at the clinic. Whether a participant linked to care will be determined by looking at the medical record, where all attended appointments are documented. If no attended appointment is documented, this will be considered non-attendance/not linked to care.

Secondary

MeasureTime frameDescription
Time to Hepatitis C Treatment Initiation6 monthsNumber of days from study enrollment to receipt of the first dose of hepatitis C treatment

Countries

United States

Participant flow

Recruitment details

Recruitment took place from July 2016 to February 2018 in an outpatient infectious disease clinic in Baltimore, Maryland

Participants by arm

ArmCount
Enhanced Usual Care
Usual clinic appointment process plus receipt of the Centers for Disease Control and Prevention (CDC) Hepatitis C Fact Sheet
33
Nurse Case Management
Nurse-initiated hepatitis C clinic referral, strengths-based education, patient navigation, appointment reminders, and care coordination of HIV/hepatitis C drug-drug interaction prevention Nurse Case Management: Participants will receive one baseline nurse case management study visit in addition to appointment reminders one week and one day before the scheduled hepatitis clinic appointment. Those who link to the Viral Hepatitis Clinic and are identified as eligible to start hepatitis C therapy by their health care provider will have one additional study visit with the nurse case manager to coordinate drug-drug interaction prevention.
35
Total68

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyBecame ineligible01
Overall StudyProtocol Violation10

Baseline characteristics

CharacteristicEnhanced Usual CareNurse Case ManagementTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
3 Participants2 Participants5 Participants
Age, Categorical
Between 18 and 65 years
30 Participants33 Participants63 Participants
Age, Continuous55.32 years
STANDARD_DEVIATION 7.73
54.76 years
STANDARD_DEVIATION 7.68
55.03 years
STANDARD_DEVIATION 7.65
Alcohol use10 Participants18 Participants28 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants0 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
31 Participants35 Participants66 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Health insurance33 Participants34 Participants67 Participants
Hepatitis C knowledge15.39 units on a scale
STANDARD_DEVIATION 2.01
14.83 units on a scale
STANDARD_DEVIATION 2.12
15.10 units on a scale
STANDARD_DEVIATION 2.07
HIV viral load15 Participants14 Participants29 Participants
Injection drug use9 Participants7 Participants16 Participants
Liver fibrosis level
Greater than or equal to F2
13 Participants11 Participants24 Participants
Liver fibrosis level
Less than F2
7 Participants7 Participants14 Participants
Liver fibrosis level
Unknown
13 Participants17 Participants30 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants0 Participants1 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
26 Participants29 Participants55 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
2 Participants0 Participants2 Participants
Race (NIH/OMB)
White
4 Participants6 Participants10 Participants
Region of Enrollment
United States
33 Participants35 Participants68 Participants
Sex: Female, Male
Female
13 Participants13 Participants26 Participants
Sex: Female, Male
Male
20 Participants22 Participants42 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 332 / 35
other
Total, other adverse events
0 / 330 / 35
serious
Total, serious adverse events
0 / 330 / 35

Outcome results

Primary

Number of Participants Linked to Care

This will be assessed based on the number of participants who attend an appointment at the Viral Hepatitis Clinic within 60 days of enrolling in the study. A participant is considered linked to care if he/she attends an appointment at the clinic. A participant is considered not linked to care if he/she does not attend an appointment at the clinic. Whether a participant linked to care will be determined by looking at the medical record, where all attended appointments are documented. If no attended appointment is documented, this will be considered non-attendance/not linked to care.

Time frame: 60 days

Population: All eligible participants who were randomized are included. Two participants were excluded (one in each arm) because they were found to be ineligible for study participation after they were randomized.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Enhanced Usual CareNumber of Participants Linked to Care8 Participants
Nurse Case ManagementNumber of Participants Linked to Care16 Participants
p-value: 0.036z-test for difference in proportions
Secondary

Time to Hepatitis C Treatment Initiation

Number of days from study enrollment to receipt of the first dose of hepatitis C treatment

Time frame: 6 months

Population: ll eligible participants who were randomized are included. Two participants were excluded (one in each arm) because they were found to be ineligible for study participation after they were randomized.

ArmMeasureValue (MEAN)Dispersion
Enhanced Usual CareTime to Hepatitis C Treatment Initiation103 daysStandard Deviation 48.5
Nurse Case ManagementTime to Hepatitis C Treatment Initiation79.3 daysStandard Deviation 26.8

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026