Medication Adherence in Human Immunodeficiency Virus (HIV)

NACompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

April 30, 2014

Primary Completion Date

July 31, 2016

Study Completion Date

July 31, 2016

Conditions
Human Immunodeficiency Virus
Interventions
BEHAVIORAL

Staff-delivered intervention sessions

In addition to standard clinical care, participants in the Pill Trial+ arm will receive staff-delivered intervention sessions individualized for each participant at HAART initiation, 1-month, and 3-month follow-up. Two booster sessions will also be provided at two weeks following intervention session 1 (in clinic) and intervention session 2 (by phone) to assess any difficulties using the created adherence plans.

OTHER

Demographic Questionnaire

Participants will complete a questionnaire developed for the purposes of the current study assessing basic background information.

OTHER

Questionnaires

Self-reported adherence, health-related quality of life and other questionnaire measures will be administered using a password protected laptop the same day as participants' regularly scheduled outpatient clinic appointments.

Trial Locations (1)

38105

St. Jude Children's Research Hospital, Memphis

All Listed Sponsors
lead

St. Jude Children's Research Hospital

OTHER

NCT02119390 - Medication Adherence in Human Immunodeficiency Virus (HIV) | Biotech Hunter | Biotech Hunter