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临床试验/NCT03149757
NCT03149757已完成不适用

Connecting Youth and Young Adults to Optimize ART Adherence: Testing the Efficacy of the Youth Thrive Intervention

University of Minnesota7 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2017年5月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
208
试验地点
7
主要终点
Visual Analog Scale (VAS) of Self-Reported Antiretroviral Adherence

研究概览

简要总结

YouTHrive (YT) is a two-arm randomized control trial (RCT) to test the efficacy of an adapted version of the Thrive With Me (TWM) intervention for youth living with HIV (YLWH). In the RCT, intervention participants will have access to the full YouTHrive (YT) website- a mobile-enhanced private social networking website aimed at improving medication adherence for YLWH. The investigators will enroll up to 60 YLWH for formative work on YT, and 300 YLWH (15-24 years old) of all genders living in eight cities and randomize them to either the intervention condition or control condition. Assessments will be collected at baseline and 5-month follow-up.

详细描述

Youth between the ages of 13 and 24 accounted for 22% of all new HIV infections in 2015. Less than half (44%) of youth living with HIV (YLWH) in the US are estimated to be virally suppressed, which is a well recognized critical factor in individual health and non-infectiousness. Given the high demands of social identity development during adolescence and early adulthood, as well as the increasing use of social media as important and influential communication channels, there is an ongoing need for innovative programs that leverage current communication channels to foster social support for ART adherence behaviors.

The investigators developed a program first called Thrive With Me (TWM) as an intervention that leverages enhanced peer-to-peer interaction, ART adherence reminders and self-monitoring, and ART and HIV informational content to improve ART adherence. Given youth's broad acceptance and adoption of many of the components of the TWM intervention, and the critical need for novel and scalable ART adherence interventions for this population, we have adapted TWM for a younger audience and all genders in a program called YouTHrive (YT).

Focus groups will provide insights into what features and functions of the current TWM study youth like and dislike to assist intervention adaptation. The investigators will conduct focus groups in three cities (Houston, Bronx, and Chicago) and will recruit up to 16 YLWH per city, and use the results to develop the YT intervention. Ahead of the RCT, the investigators will conduct usability testing on YT to gain feedback about the developed intervention. The investigators will recruit 12 YLWH in six cities to use the intervention for a two-week period for usability testing.

The randomized controlled efficacy trial will compare YT (N=150) to a control group (N=150). YLWH in the control arm will receive weekly static information-only emails, compared to daily use of the dynamic YT social network site for the intervention group. Participants will be recruited from eight cities: Atlanta, New York, Chapel Hill, Charlotte, Chicago, Houston, Philadelphia, and Tampa. Assessments will be collected at baseline and 5-month follow-up.

Specific Aims include:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Care Provider, Investigator)

入排标准

年龄范围
15 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •15-24 years of age at the enrollment visit;
  • •HIV-positive status;
  • •Residing in Chicago, Houston, NYC, Philadelphia, Atlanta, Tampa, or Raleigh/Durham/Chapel Hill areas and available to meet in-person or virtually with SRV staff for visits at baseline and 5-month follow-up assessment;
  • •English-speaking (since the intervention will be in English);
  • •Anticipated continuous internet access and SMS messaging for the intervention period (approximately 5 months);
  • •Not enrolled in another ART adherence intervention research study at the time of screening;
  • •Has or is willing to create an e-mail address to use during the study period;
  • •Did not attend an iTech Youth Advisory Board (YAB) or Youth Advisory Council (YAC) meeting where the YouTHrive study was presented or YouTHrive study materials were discussed.

排除标准

  • •Is younger than 15 years old or older than 24 years old at the enrollment visit;
  • •does not have an HIV-positive status;
  • •Does not reside in Chicago, Houston, NYC, Philadelphia, Atlanta, Tampa, or Raleigh/Durham/Chapel Hill areas and not available to meet with SRV staff for visits at baseline, and 5-month follow-up assessment;
  • •Does not speak English;
  • •Does not anticipate having continuous internet access and SMS messaging for the intervention period (approximately 5 months);
  • •Is enrolled in another ART adherence intervention research study at the time of screening;
  • •Does not have or is not willing to create an e-mail address to use during the study period;
  • •Is a member of an iTech Youth Advisory Board (YAB) or Youth Advisory Council (YAC).
  • •Participants who are or become pregnant during the study period will not be excluded.

研究组 & 干预措施

YouTHrive

Experimental

YouTHrive is a five-month technology-based intervention that uses peer-to-peer interaction, daily self-monitoring, and tailored content to address barriers to HIV medication adherence.

干预措施: YouTHrive (Behavioral)

Thrive Tips

Active Comparator

Participants randomized to the control condition will receive a weekly email with static informational content about living with HIV and general well being.

干预措施: Information-only Control (Behavioral)

结局指标

主要结局

Visual Analog Scale (VAS) of Self-Reported Antiretroviral Adherence

时间窗: 5-month follow-up

Participants were presented with a visual analog scale (VAS) of the percentage of antiretroviral therapy (ART) adherence in the past 30 days on a scale from 0% to 100% (with 10% increments as response options) and asked to choose the level of ART adherence they achieved in the past 30 days. The mean percentage of ART adherence across all participants was calculated.

次要结局

  • Percentage of Participants With Undetectable HIV Viral Load(5-month follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

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