Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:28 PM
Ignite Modification Date:
2025-12-24 @ 5:28 PM
NCT ID:
NCT01049568
Eligibility Criteria:
Inclusion Criteria:
Documented HIV-positive infected either behaviorally or perinatally as determined by medical record review or verbal verification from referring professional.
Age 15 and 0 days to 24 years and 364 days. Enrolled in care at an AMTU or affiliated site.
History of non-adherence to one or more components of antiretroviral therapy, defined as meeting one of the following criteria:
* Currently prescribed HAART and reports to care provider less than 90% adherence in previous month and has viral load greater than 1000 copies/ml when last evaluated (within the last four weeks);
* Discontinued HAART in the past while documented to be less than 90% adherent during the most recent antiretroviral treatment; and
* Agreed to initiate antiretroviral treatment in the past, but never initiated. Able to speak and understand English. Willing to provide informed consent or assent.
Exclusion Criteria:
Evidence of cognitive impairment or other mental condition (including substance abuse) that limits his/her ability to complete intervention and assessments (per PI or designee discretion). Participants with stable and treated mental health/substance abuse disorders are acceptable for inclusion with protocol team approval.
Any condition, including active substance abuse that is expected to limit the likelihood that the participant may maintain involvement for the entire year on-study (per PI or designee discretion with protocol team approval).
No participant consent, parental permission or youth assent (as appropriate). Minors unable to acquire parental/guardian consent, even if not living at home, will not be able to participate as a change in housing status during the study might require premature discontinuation.
Current participation in another behavioral interventional trial.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
15 Years
Maximum Age:
24 Years
Study:
NCT01049568
Study Brief:
Protocol Section:
NCT01049568