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Digital Star: HIV Prevention for Youth in Mental Health Treatment (DSTAR)

Primary Purpose

Human Immunodeficiency Virus, Mental Health

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
D*STAR
D*HEALTH
Sponsored by
Rhode Island Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Human Immunodeficiency Virus focused on measuring Adolescents, HIV prevention, computerized intervention, mental health treatment

Eligibility Criteria

13 Years - 20 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Adolescent males and females ages 13 to 20 years who are in mental health treatment will be eligible for enrollment in each phase of study according to the following criteria:

  1. English speaking,
  2. adolescent assent given to participate in the study,
  3. consent of a parent/legal guardian and HIPAA research authorization permission and
  4. attending an alternative / therapeutic school, mental health day treatment program, partial hospital program, or therapeutic group homes.

Exclusion Criteria:

  1. self-report of HIV infection (STAR is not designed to address disclosure, stigma, and medical adherence issues),
  2. recent or current pregnancy,
  3. cognitive limitation that impairs consent capacity by judgment of clinical staff and
  4. current participation in another psychosocial intervention that is addressing STI/HIV prevention.

Sites / Locations

  • Rhode Island Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

DSTAR

DHEALTH

Arm Description

Digital HIV Prevention intervention developed to specifically address the needs of youth in mental health treatment. Sessions introduce affect regulation and cognitive monitoring in sexual situations, and provide basic sexual health skills and education.

Digital general health promotion intervention. Time and attention matched intervention that targets health behaviors relevant to youth including exercise, nutrition, sleep, and smoking. Basic information about HIV and sexuality is also included.

Outcomes

Primary Outcome Measures

HIV Knowledge
HIV Knowledge Questionnaire. A 18-item (true, false, uncertain) scale surveys routes of transmission, casual contact misconceptions, general information and course of illness. Scores range from 0-18 with higher scores indicating greater HIV knowledge.
Self-efficacy for HIV Prevention
The scale contains 13 items that reflect the context of condom use, such as "could use a condom when I'm very upset". Scores range from 13 to 52 with higher scores indicated lower self-efficacy for HIV prevention.
Lifetime Sexual Intercourse
Lifetime oral, vaginal, and/or anal sex
Recent Oral, Vaginal, and/or Anal Sex
Oral, vaginal, and/or anal sex in the past 3 months
Frequency of Sexual Intercourse
Number of oral, vaginal, and/or anal sexual occurrences in the past 3 months.
Number of Sexual Partners
Number of sexual partners in the past 3 months.
Frequency of Condom Use
Number of times a condom was used during oral, vaginal, and/or anal sex
Condom Use Intention
On a scale of 0 to 100, participants report how likely it is that they will use a condom when they have sex in the next 3 months. Zero represented "I will not use a condom", "50" represented "I will use a condom half the time.", and "100" represented "I will use a condom all the time.".
Recent Alcohol Use
Alcohol use in the past 30 days (yes/no)
Frequency of Recent Alcohol Use
Number of days alcohol was used in the past 30 days
Quantity of Recent Alcohol Use
Number of drinks reported on days that a participant drank alcohol in the past 30 days
Recent Marijuana Use
Marijuana use in the past 30 days (yes/no)
Frequency of Recent Marijuana Use
Number of days marijuana was used in the past 30 days

Secondary Outcome Measures

Affect Dysregulation Scale
A six-item scale assessing adolescents' perceived abilities to manage emotional upset (e.g., "In the past three months, I have had trouble controlling my feelings.") in sexual situations. Scores range from 6 to 24 with higher scores indicated poorer perceived ability to manage emotional upset in sexual situations.

Full Information

First Posted
September 29, 2016
Last Updated
January 15, 2020
Sponsor
Rhode Island Hospital
Collaborators
Virtually Better, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02921841
Brief Title
Digital Star: HIV Prevention for Youth in Mental Health Treatment
Acronym
DSTAR
Official Title
Digital Star: HIV Prevention for Youth in Mental Health Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
November 2016 (undefined)
Primary Completion Date
March 2019 (Actual)
Study Completion Date
July 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rhode Island Hospital
Collaborators
Virtually Better, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Teenagers in mental health treatment are at greater risk for HIV and other sexually transmitted infections. This greater risk comes from many factors, some of which are related to poor emotion regulation and low self-confidence. There is a need for an HIV prevention program specifically for these at-risk teens. The goal of this study is to develop a computerized HIV prevention study tailored to adolescents in mental health treatment. The first part of the study will develop core sessions of D*STAR. It will do this by using focus group feedback from approximately 15 adolescents in mental health treatment, and approximately 10 parents of youth in mental health treatment and mental health treatment center staff. Feedback on D*STAR prototype sessions will also be collected from two individual interviews with approximately 15 youth in mental health treatment. Core sessions will then be reviewed in an open trial with approximately 30 adolescents. The second part of the study will develop and refine digital versions of the remaining sessions of STAR and a digital general health promotion intervention. It will do this by using focus group feedback from approximately 20 adolescents in mental health treatment, and approximately 10 community advisory board members which include variety of staff from mental health treatment settings such as administrators, supervisors, therapists, health teachers at therapeutic schools, clinicians at day hospitals and day treatment programs, parents of youth in mental health treatment and from relevant community organizations, such as those serving lesbian, gay, bisexual, transgender, and questioning youth. Feedback on D*STAR prototype sessions will also be collected from two individual interviews with approximately 20 youth in mental health treatment. All developed sessions (from both Phase I and Phase II) will then be reviewed in an open trial with approximately 20 adolescents. A randomized control trial (RCT) will then be conducted to compare D*STAR to a time matched digital general health promotion intervention among approximately 120 adolescents. For the pilot and RCT phases, assessments will be administered prior to randomization, immediately following the last intervention session, and at one month post-intervention (pilot study) or at three month post-intervention (RCT).
Detailed Description
Adolescents in mental health treatment are at greater risk for HIV and other STIs than their peers due to an earlier age of onset of sex, less protected sex, more sexual partners, and more frequent substance use. The numerous adolescents who receive mental health treatment do so in a variety of settings such as day hospital programs, therapeutic schools and residential centers. These programs offer a variety of health services but there is no efficacious HIV prevention program specifically tailored for the issues of youth in mental health treatment, other than the one described in this project. STAR ("Safe Thinking and Affect Regulation"). The goal of this SBIR (Small Business Innovation Research) Fast-Track project is to transform STAR into an engaging digital, multimedia format, Digital STAR (D*STAR), for easy and reliable use by care agencies that serve adolescents in mental health treatment. To transform this intervention, Virtually Better, a company with a successful history of production and distribution of cutting-edge technological interventions, has teamed with the research developers of STAR at Rhode Island Hospital and Brown University. During the two phases of this Fast-Track project, digital session development will be accomplished by an iterative process of feedback and refinement between Virtually Better, the developers of STAR, adolescents in mental health treatment, and a Community Advisory Board. Phase 1: Specific Aims A. To develop and refine digital versions of core sessions of STAR that introduce affect regulation and cognitive monitoring in sexual situations, and provide basic sexual health skills and education. These sessions represent essential content areas and modalities of the D*STAR intervention. B. To conduct focus groups of the feasibility, utility, and acceptability of the planned sessions. There will be focus groups with approximately 10 Community Advisory Board (CAB) members comprised of parents of youth in mental health treatment and mental health treatment staff. There will also be focus groups with approximately 15 adolescents in mental health treatment (13-18 years old) . C. To conduct two qualitative interview sessions of approximately 15 youth with mental health treatment to determine the acceptability of the session's prototypes and revise based on feedback. D. To conduct an open trial of D*STAR sessions with approximately 30 adolescents to determine its preliminary impact with self-report assessments at baseline and then 1 month post intervention. Phase 2: Specific Aims A. To develop and refine digital versions the remaining sessions of STAR and a digital general health promotion (HP) intervention, building upon the essential content areas and refinements developed in Phase I. B. To conduct qualitative evaluations of the feasibility, utility, and acceptability of D*STAR and the digital HP intervention with adolescents in mental health treatment, our Community Advisory Board (CAB), and mental health treatment center staff. Hypothesis: Both digital interventions (HP and D*STAR) will be rated by youth, our CAB, and mental health treatment center staff as enjoyable, useful and easy to implement. C. To conduct a randomized control trial of D*STAR compared to the time matched digital HP intervention among 120 adolescents ages 13 to 18 in mental health treatment. Hypothesis: Participants in D*STAR will report safer sexual behaviors, greater HIV knowledge and greater self-efficacy for HIV prevention skills than participants in digital HP at three months follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Immunodeficiency Virus, Mental Health
Keywords
Adolescents, HIV prevention, computerized intervention, mental health treatment

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
125 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DSTAR
Arm Type
Experimental
Arm Description
Digital HIV Prevention intervention developed to specifically address the needs of youth in mental health treatment. Sessions introduce affect regulation and cognitive monitoring in sexual situations, and provide basic sexual health skills and education.
Arm Title
DHEALTH
Arm Type
Active Comparator
Arm Description
Digital general health promotion intervention. Time and attention matched intervention that targets health behaviors relevant to youth including exercise, nutrition, sleep, and smoking. Basic information about HIV and sexuality is also included.
Intervention Type
Behavioral
Intervention Name(s)
D*STAR
Intervention Type
Behavioral
Intervention Name(s)
D*HEALTH
Intervention Description
Digital general health promotion intervention. Time and attention matched intervention that targets health behaviors relevant to youth including exercise, nutrition, sleep, and smoking. Basic information about HIV and sexuality is also included.
Primary Outcome Measure Information:
Title
HIV Knowledge
Description
HIV Knowledge Questionnaire. A 18-item (true, false, uncertain) scale surveys routes of transmission, casual contact misconceptions, general information and course of illness. Scores range from 0-18 with higher scores indicating greater HIV knowledge.
Time Frame
3 months post-intervention
Title
Self-efficacy for HIV Prevention
Description
The scale contains 13 items that reflect the context of condom use, such as "could use a condom when I'm very upset". Scores range from 13 to 52 with higher scores indicated lower self-efficacy for HIV prevention.
Time Frame
3 months post-intervention
Title
Lifetime Sexual Intercourse
Description
Lifetime oral, vaginal, and/or anal sex
Time Frame
3-months post-intervention
Title
Recent Oral, Vaginal, and/or Anal Sex
Description
Oral, vaginal, and/or anal sex in the past 3 months
Time Frame
3-months post-intervention
Title
Frequency of Sexual Intercourse
Description
Number of oral, vaginal, and/or anal sexual occurrences in the past 3 months.
Time Frame
3-months post-intervention
Title
Number of Sexual Partners
Description
Number of sexual partners in the past 3 months.
Time Frame
3-months post-intervention
Title
Frequency of Condom Use
Description
Number of times a condom was used during oral, vaginal, and/or anal sex
Time Frame
3-months post-intervention
Title
Condom Use Intention
Description
On a scale of 0 to 100, participants report how likely it is that they will use a condom when they have sex in the next 3 months. Zero represented "I will not use a condom", "50" represented "I will use a condom half the time.", and "100" represented "I will use a condom all the time.".
Time Frame
3-months post-intervention
Title
Recent Alcohol Use
Description
Alcohol use in the past 30 days (yes/no)
Time Frame
3-months post-intervention
Title
Frequency of Recent Alcohol Use
Description
Number of days alcohol was used in the past 30 days
Time Frame
3-months post-intervention
Title
Quantity of Recent Alcohol Use
Description
Number of drinks reported on days that a participant drank alcohol in the past 30 days
Time Frame
3-months post-intervention
Title
Recent Marijuana Use
Description
Marijuana use in the past 30 days (yes/no)
Time Frame
3-months post-intervention
Title
Frequency of Recent Marijuana Use
Description
Number of days marijuana was used in the past 30 days
Time Frame
3-months post-intervention
Secondary Outcome Measure Information:
Title
Affect Dysregulation Scale
Description
A six-item scale assessing adolescents' perceived abilities to manage emotional upset (e.g., "In the past three months, I have had trouble controlling my feelings.") in sexual situations. Scores range from 6 to 24 with higher scores indicated poorer perceived ability to manage emotional upset in sexual situations.
Time Frame
3 months post-intervention (average 6 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adolescent males and females ages 13 to 20 years who are in mental health treatment will be eligible for enrollment in each phase of study according to the following criteria: English speaking, adolescent assent given to participate in the study, consent of a parent/legal guardian and HIPAA research authorization permission and attending an alternative / therapeutic school, mental health day treatment program, partial hospital program, or therapeutic group homes. Exclusion Criteria: self-report of HIV infection (STAR is not designed to address disclosure, stigma, and medical adherence issues), recent or current pregnancy, cognitive limitation that impairs consent capacity by judgment of clinical staff and current participation in another psychosocial intervention that is addressing STI/HIV prevention.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margo Adams Larsen, PhD
Organizational Affiliation
Virtually Better, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rhode Island Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States

12. IPD Sharing Statement

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