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Enhancing Communication and HIV Outcomes

Enhancing Communication and HIV Outcomes

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00675610
Acronym
ECHO
Enrollment
186
Registered
2008-05-09
Start date
2008-05-31
Completion date
2010-05-31
Last updated
2015-04-01

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

Conditions

HIV Infections

Keywords

communication, HIV/AIDS, Treatment Experienced

Brief summary

The goal of this research is to improve communication between the patients with HIV and their health care providers. The overall purpose of doing so is to reduce disparities in medication self-efficacy, adherence to therapy, and HIV viral load suppression. The investigators will conduct a randomized controlled trial to test the effectiveness of a combined provider and patient communication intervention conducted at two separate visits compared to usual care in improving the quality of patient-provider communication, patients' medication self-efficacy, patient adherence to therapy, and HIV RNA suppression.

Detailed description

The goal of this research is to improve communication between the patients with HIV and their health care providers. The overall purpose of doing so is to reduce disparities in medication self-efficacy, adherence to therapy, and HIV viral load suppression. We will conduct a randomized controlled trial to test the effectiveness of a combined provider and patient communication intervention conducted at two separate visits compared to usual care in improving the quality of patient-provider communication, patients' medication self-efficacy, patient adherence to therapy, and HIV RNA suppression. The following primary and secondary hypotheses will be addressed. Primary Hypothesis. 1\) There will be more and higher quality patient-provider communication about antiretroviral medication adherence in the intervention compared to control arm at both visit 1 (V1) and visit 2 (V2). Secondary Hypotheses 1. Higher quality patient-provider communication in the intervention arm will be associated with * higher patient ratings of communication (overall, HIV-specific, adherence-specific, and interpersonal style of provider) at V1 and V2; * increased patient preference for a shared decision-making role at V1 and V2; * more positive health beliefs at V1 and V2; * higher patient medication self-efficacy at V1 and V2; * better adherence to antiretroviral medication (assessed by 3-day recall) at V2; and * a greater percentage of patients with HIV-1 RNA suppression at V2. 2. The intervention will reduce disparities in medication self-efficacy, adherence, and HIV-1 RNA suppression.

Interventions

providers are trained to communicate with patients about adherence and patients are coached to discuss adherence with providers

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

(Providers): 1. Currently providing primary care to at least 10 HIV-infected patients in the clinic 2. Physician, Nurse-Practitioner, or Physician-Assistant 3. Agree to give written informed consent. Inclusion Criteria (Patients): 1. HIV-infected patient of one of the participating providers 2. Has had at least one prior visit with that provider 3. Currently taking antiretroviral therapy 4. Capable of understanding and giving written informed consent 5. Age \> 20 years old 6. English-speaking 7. African-American (or people of African descent living in the United States), Hispanic, or non-Hispanic White race/ethnicity

Design outcomes

Primary

MeasureTime frame
patient-provider communication1 day- 3 months

Countries

United States

Outcome results

None listed

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