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Improving Antiretroviral Medication Adherence Among HIV-infected Youth: Phase I

This study has been completed.
Sponsor:
Collaborators:
Massachusetts General Hospital
Boston Children’s Hospital
Harvard Medical School
Information provided by (Responsible Party):
Matthew Mimiaga, Fenway Community Health
ClinicalTrials.gov Identifier:
NCT01253850
First received: December 2, 2010
Last updated: April 13, 2017
Last verified: April 2017
December 2, 2010
April 13, 2017
August 2010
July 2011   (Final data collection date for primary outcome measure)
perceived barriers and facilitators to adherence [ Time Frame: One-time qualitative interview ]
We will code the qualitative interview data for key themes that emerge with respect to adherence and intervention needs. The information obtained from the qualitative interviews is used to adapt the Life-Steps intervention (designed by our group for HIV-infected adults) to be responsive to the needs of HIV-infected adolescents, with acceptability of topics and content, and feasibility of intervention delivery to be tested in an open pilot trial.
HIV antiretroviral medication adherence [ Time Frame: 3 months ]
Complete list of historical versions of study NCT01253850 on ClinicalTrials.gov Archive Site
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Improving Antiretroviral Medication Adherence Among HIV-infected Youth: Phase I
Improving Antiretroviral Medication Adherence Among HIV-infected Youth: Phase I

HIV is increasing among adolescents and young adults in the US. Antiretroviral medications, when taken correctly (≥90% of prescribed doses taken), can vastly improve life expectancy. However, adherence among HIV-infected young people is suboptimal, and few interventions are available to help adolescents adhere to treatment.

The first phase of the study is an intervention development phase, which includes conducting interviews with 40 HIV-infected youth for input on the adaptation of the approach. The information obtained from the qualitative interviews is used to adapt the Life-Steps intervention (designed by our group for HIV-infected adults) to be responsive to the needs of HIV-infected adolescents, with acceptability of topics and content, and feasibility of intervention delivery to be tested in an open pilot trial.

This phase of the protocol focuses on setting up the infrastructure necessary for conducting the study, including hiring and training activities with study staff. This time will be spent conducting interviews and using these data to inform the development of the intervention protocol and adaptation of all Life-Steps intervention materials, including study assessment instruments, for HIV-infected youth.

The interview is a one-time event and will last for 1.5-2 hours. It has two components: a quantitative assessment and a qualitative discussion. After all participants have completed the informed consent and assent (if under the age of 18) processes, the research staff will administer a brief quantitative assessment that will ask questions related to demographics, medication adherence, sexual risk, substance use, and psychosocial condition. The second part of the interview will be an open discussion. The interviews will be conducted by a trained member of the research staff. The interviews will be informed by a pre-determined qualitative topic guide.

Observational
Observational Model: Cohort
Time Perspective: Other
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Non-Probability Sample
HIV-infected youth between the ages of 13 and 24
HIV Infection
Not Provided
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Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
31
March 6, 2013
July 2011   (Final data collection date for primary outcome measure)

Phase I

Inclusion Criteria:

  • Age 13 to 24 years
  • HIV-infected and aware of HIV-infection status
  • Currently taking antiretroviral therapy, has been prescribed antiretroviral therapy in the past 6 months, or a medical provider has recommended antiretroviral medications within the last 6 months
  • Willing and able to provide informed consent or assent (if under the age of 18)

Exclusion Criteria:

  • Not willing or able to provide informed consent or assent (if under the age of 18)
  • Is dealing with a severe mental illness requiring immediate treatment (e.g. active psychotic episode) or a mental illness that would limit a participant's ability to engage with study protocol (e.g. dementia)
  • Has severe cognitive limitations that would limit a participant's ability to comprehend the informed consent or assent.

Phase II

Inclusion Criteria:

  • Age 13-24 years
  • HIV-infected and aware of HIV-infection status
  • Currently taking antiretroviral therapy
  • Self-reported difficulties adhering to HIV medications in the past 3 months
  • Self-identify as heterosexual or LGB
  • Willing and able to provide informed consent/consent of parent/guardian if under the age of 18

Exclusion Criteria:

  • Not willing or able to provide informed consent or assent (if under the age of 18)
  • Is dealing with a severe mental illness requiring immediate treatment (e.g. active psychotic episode) or a mental illness that would limit a participant's ability to engage with study protocol (e.g. dementia)
  • Has severe cognitive limitations that would limit a participant's ability to comprehend the informed consent or assent.
Sexes Eligible for Study: All
13 Years to 24 Years   (Child, Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01253850
CFAR Adherence HIV Youth:1
Yes
Not Provided
Plan to Share IPD: No
Matthew Mimiaga, Fenway Community Health
Fenway Community Health
  • Massachusetts General Hospital
  • Boston Children’s Hospital
  • Harvard Medical School
Principal Investigator: Matthew J. Mimiaga, ScD MPH Fenway Health and Massachusetts General Hospital
Fenway Community Health
April 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP