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Intervention for Human Immunodeficiency Virus Infection
N/A
Waitlist Available
Led By Michael Wohlfeiler, MD
Research Sponsored by Epividian
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 9
Awards & highlights
Study Summary
This study is evaluating whether a system of alerts can help providers manage the scheduling of monthly cabotegravir + rilpivirine long-acting injections for the treatment of HIV.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9 month
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 month
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Acceptability and usefulness of the intervention
Adherence to treatment-window
Secondary outcome measures
Number of CAB+RPV LA patients managed through the app
Number of clinics that use the App for the management of CAB+RPV LA patients
Trial Design
2Treatment groups
Active Control
Group I: InterventionActive Control1 Intervention
Clinics randomized to the intervention. A notification will be sent to the provider when a patient on CAB+RPV LA needs to be scheduled for their injections or when an appointment needs to be confirmed. Alerts are sent out to the provider when a patient is due or overdue for their injections.
Group II: ControlActive Control1 Intervention
Clinics randomized to the control group. No alerts or notification will be sent. The providers will manage their CAB+RPV LA patients using standard of care in their clinic.
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Who is running the clinical trial?
EpividianLead Sponsor
7 Previous Clinical Trials
2,144,756 Total Patients Enrolled
AIDS Healthcare FoundationOTHER
17 Previous Clinical Trials
145,634 Total Patients Enrolled
ViiV HealthcareIndustry Sponsor
359 Previous Clinical Trials
468,506 Total Patients Enrolled
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