FOCUS - INACTIVE

Inactive Reason
This program is inactive because it has evidence of favorable impacts that is more than 20 years old. It no longer meets the inclusion criteria for the TPPER.
Developers
Cherrie Boyer, Ph.D., Mary-Ann Shafer, M.D., and Richard Shaffer, Ph.D.
Program Summary
FOCUS is an eight-hour cognitive-behavioral group intervention that promotes healthy behavior and responsible decision-making among young women. The program covers topics such as responsible behavior, relationships, pregnancy prevention, and STI prevention.
Intended Population
The suggested target population is youth who are at least 17 years old. It was evaluated with female United States Marine Corps recruits, ages 17 and older.
Program Setting

FOCUS was designed to be delivered in diverse program settings. It was evaluated in a classroom-based setting during the first 13-week period of Marine recruit training.

Contact and Availability Information
Sociometrics Corporation
1580 W. El Camino Real, Suite 8
Mountain View, CA 94040
Ph: 650-949-3282
Email: socio@socio.com
Website: https://www.socio.com/products/pasha-focus-preventing-sexually-transmitted-infections-and-unwanted-pregnancies-among-young-women
Sample of Curriculum Available for Review Prior to Purchase
No
Languages Available
English
Monitoring and Evaluation Tools
Monitoring and evaluation tools available
Yes
Monitoring and evaluation tool usage required
No
Information about available monitoring and evaluation tools (if applicable)

FOCUS has a fidelity toolkit and checklist, tools for monitoring program implementation, and evaluation instruments. Telephone technical support on implementation and evaluation is also provided by Sociometrics for one year with purchase of the program materials. 

Program Components and Core Components

Last updated in 2024

The data presented on this page reflect responses from the program’s developer or distributor to a program component checklist that asked them to report on the individual components within their TPP program. The same program component checklist was sent to the developer or distributor of every active TPP program with evidence of effectiveness. The program component table provides information on seven types of program components including content, delivery mechanism, dosage, staffing, format, context, and intended population characteristics; whether the component was present or optional in the program; whether the component is considered to be core to the program; and the lesson number or activity where the component can be found in the program. In the drop-down menu below, under “Has component,” there are four options that indicate a component as present in the program: (1) “Yes” indicates that the component is present in at least one version of the program (whether that be the program version that was evaluated, the current version, or both versions); (2) “Yes (both versions)” indicates that the component is present in both the evaluated version of the program and the current version of the program; (3) “Yes (current version)” indicates that the component is present in the current, but not the evaluated, version of the program; and (4) “Yes (evaluated version)” indicates that the component is present in the evaluated version of the program, only. Note that for dosage components, the only possible response option was “Yes”, and the dosage is described in the Notes when available. For more details, refer to the FAQ. Some of the components identified are noted as core components of the evidence-based program, but this does not necessarily mean that these components have been rigorously tested and show evidence of effectiveness. Most often developers denoted components as core based on theory or experience in the field. Click here for the list of evidence-based components.

Category Component Core Component Component present Notes Lesson number(s) / activities where present
Content Substance use cessation No
Content Boundary setting/refusal skills No Yes (evaluated version)
Content Child development No
Content Communication skills Yes Yes (evaluated version)
Content Conflict resolution/social problem solving No
Content Cultural values No Yes (evaluated version)
Content Gender identity No
Content Gender roles Yes Yes (evaluated version)
Content Leadership No
Content Normative beliefs Yes Yes (evaluated version)
Content Parenting skills No
Content Social competence
Content Social influence/actual vs. perceived social norms No Yes (evaluated version)
Content Social support/capital No
Content Identity development No
Content Morals/values No Yes (evaluated version)
Content Spirituality No
Content Volunteering/civic engagement No
Content Other
Delivery mechanism Method: Anonymous question box No
Delivery mechanism Method: Artistic expression No
Delivery mechanism Method: Assessment/survey Yes Yes (evaluated version)
Delivery mechanism Method: Booster session No
Delivery mechanism Method: Case management No
Delivery mechanism Method: Cognitive behavioral therapy (CBT) No
Delivery mechanism Method: Demonstration Yes Yes (evaluated version)
Delivery mechanism Method: Discussion/debrief Yes (evaluated version)
Delivery mechanism Method: Family session No
Delivery mechanism Method: Game No
Delivery mechanism Method: Home visiting No
Delivery mechanism Method: Homework assignment No
Delivery mechanism Method: In-session assignment No Yes (evaluated version)
Delivery mechanism Method: Introduction Yes Yes (evaluated version)
Delivery mechanism Method: Lecture Yes Yes (evaluated version)
Delivery mechanism Method: Motivational interviewing No
Delivery mechanism Method: Music No
Delivery mechanism Method: Parent-focused activity No
Delivery mechanism Method: Peer-to-peer Yes Yes (evaluated version)
Delivery mechanism Method: Public service announcement No Yes (evaluated version)
Delivery mechanism Method: Reading No Yes (evaluated version)
Delivery mechanism Method: Role play/Practice Yes Yes (evaluated version)
Delivery mechanism Method: Self-guided activity No
Delivery mechanism Method: Service learning No
Delivery mechanism Method: Slide show Yes Yes (evaluated version)
Delivery mechanism Method: Social media No
Delivery mechanism Method: Spiral learning No
Delivery mechanism Method: Storytelling Yes (evaluated version)
Delivery mechanism Method: Text message No
Delivery mechanism Method: Video
Delivery mechanism Method: Other
Program Objectives
FOCUS seeks to prevent unintended pregnancy and STIs among young women, ages 17 and older. It is designed to change attitudes about sexual behavior, improve knowledge about pregnancy and STIs, and build communications skills including contraceptive use and refusal skills.
Program Content

The core content includes four 2-hour sessions. The sessions are broken into modules, which can be delivered separately.

  • Session 1: Increase knowledge about unintended pregnancies and STDs including HIV/AIDS. Goal: Modify values, beliefs, and attitudes that impact sexual behavior.
  • Session 2: Increase knowledge about hormonal and barrier contraceptives. Goal: Build communication skills to prevent risky sexual behaviors and increase condom use.
  • Session 3: Increase knowledge about the signs, symptoms, and consequences of STDs/HIV/AIDS. Goals: Increase knowledge about the transmission and prevention of STDs/HIV; Build communication skills to prevent STDs/HIV.
  • Session 4: Modify attitudes about the effects of alcohol and its relationship to sexual risk behaviors. Goals: Build refusal communication skills; Build condom use skills; Increase awareness about how life choices can impact decision-making and health.
Program Methods
The program is primarily delivered through lectures using PowerPoint slide presentations. Presentations are augmented by group discussions, interactive activities including a condom demonstration, role play, and videos.
Program Structure and Timeline

The eight-hour curriculum is designed to be delivered in four 2-hour sessions. Groups should be 20 to 25 participants.

Staffing

FOCUS facilitators are preferably female health educators or facilitators comfortable with sexual health subject matter.

Staff Training
There is no required training for this program. Providers interested in training should contact Sociometrics.
Program Materials and Resources
The following program materials are available through the distributor:
  • User's Guide
  • Program Manual
  • 1 Flash Drive Containing 11 Power Point Slide Sets
  • 1 copy of each of these 4 DVDs: (1) Birth Control: Understanding the Options, (2) My First Pelvic Exam, (3) In Our Own Words: Teens and AIDS, (4) Good to Go.
  • Video list
  • 50 copies of two brochures (STD Facts and Birth Control Facts)
  • Photocopy masters of all handouts
  • Fidelity toolkit
  • Original Evaluation Instruments booklet
  • Prevention Minimum Evaluation Data Set (PMEDS)
  • Local Evaluator Consultant Network Directory

While a free sample curriculum is not available, providers may purchase an automatic digital download of the user’s guide to review program components, core competencies for facilitators, and scientific evidence of effectiveness. If providers decide to purchase the program, the price of the download is deducted.

Additional Needs for Implementation

The program requires the use of a television and DVD player, a computer with PowerPoint capabilities, and a screen for showing PowerPoint presentations. Other materials needed for implementation include condoms, a penis proxy, and hard candies.

Fidelity
FOCUS has a fidelity toolkit/checklist and tools for monitoring program implementation. It may be accessed on the Sociometrics website: https://www.socio.com/products/pasha-focus-preventing-sexually-transmitted-infections-and-unwanted-pregnancies-among-young-women
 
Technical Assistance and Ongoing Support
Sociometrics provides telephone technical support on implementation and evaluation for one year with purchase of the program materials.
Allowable Adaptations

There are three allowable adaptations, however, all adaptations must be approved by the developer and Sociometrics. Potential adaptations include: 

  • The program can be implemented in different settings, such as clinics, community-based organizations, or schools/colleges.
  • The program can be adapted for use with non-military women. This program cannot be adapted for men.
  • It may be possible to deliver the sessions in longer or shorter segments.
Adaptation Guidelines or Kit
No
Reviewed Studies
Citation High-Quality Randomized Trial Moderate-Quality Randomized Trial Moderate-Quality Quasi-Experiment Low Study Rating Did Not Meet Eligibility Criteria

Flinders n.d.

Boyer et al. 2005

Flinders 2013a

Flinders 2013b

Flinders 2013c

Flinders 2013d

Flinders et al. 2014

Bernstein and Flinders 2017

Flinders 2017

Flinders and Zehler 2022

Study Characteristics
Citation Setting Majority Age Group Majority Racial/Ethnic Group Gender Sample Size

Flinders n.d.

n.a. n.a. n.a. n.a. n.a.

Boyer et al. 2005

Specialized setting 18 or 19 White Young women

2157

Flinders 2013a

n.a. n.a. n.a. n.a. n.a.

Flinders 2013b

n.a. n.a. n.a. n.a. n.a.

Flinders 2013c

n.a. n.a. n.a. n.a. n.a.

Flinders 2013d

n.a. n.a. n.a. n.a. n.a.

Flinders et al. 2014

n.a. n.a. n.a. n.a. n.a.

Bernstein and Flinders 2017

n.a. n.a. n.a. n.a. n.a.

Flinders 2017

n.a. n.a. n.a. n.a. n.a.

Flinders and Zehler 2022

n.a. n.a. n.a. n.a. n.a.
Study Findings

Evidence by Outcome Domain and Study

Citation Sexual Activity Number of Sexual Partners Contraceptive Use STIs or HIV Pregnancy

Flinders n.d.

n.a. n.a. n.a. n.a. n.a.

Boyer et al. 2005

n.a. Potentially favorable evidence Indeterminate evidence n.a. n.a.

Flinders 2013a

n.a. n.a. n.a. n.a. n.a.

Flinders 2013b

n.a. n.a. n.a. n.a. n.a.

Flinders 2013c

n.a. n.a. n.a. n.a. n.a.

Flinders 2013d

n.a. n.a. n.a. n.a. n.a.

Flinders et al. 2014

n.a. n.a. n.a. n.a. n.a.

Bernstein and Flinders 2017

n.a. n.a. n.a. n.a. n.a.

Flinders 2017

n.a. n.a. n.a. n.a. n.a.

Flinders and Zehler 2022

n.a. n.a. n.a. n.a. n.a.
KEY
Evidence Indication
Favorable findings
Two or more favorable impacts and no unfavorable impacts, regardless of null findings
Potentially favorable findings
At least one favorable impact and no unfavorable impacts, regardless of null findings
Indeterminate findings
Uniformly null findings
Conflicting findings
At least one favorable and at least one unfavorable impact, regardless of null findings
Potentially unfavorable findings
At least one unfavorable impact and no favorable impacts, regardless of null findings
Unfavorable findings
Two or more unfavorable impacts and no favorable impacts, regardless of null findings
Note: n.a. indicates the study did not examine any outcome measures within that particular outcome domain, or the study examined outcome measures within that domain but the findings did not meet the review evidence standards.
Detailed Findings
Citation Details

Flinders n.d.

This study did not meet the review's eligibility criteria

Boyer et al. 2005

The program was evaluated in a cluster randomized controlled trial involving female Marine recruits who participated in the study during their first 13-week training period. Study participants were randomly assigned by platoon to either a treatment group that received the FOCUS intervention or a control group that received a health-promotion intervention on diet, physical activity, and cancer prevention. Surveys were administered immediately before the program (baseline) and at approximately one and eleven months after the program ended. Biological screening was conducted for pregnancy, chlamydia, gonorrhea, and trichomonas.

The study found that 11 months after the program ended, participants in the intervention who were sexually inexperienced at baseline were significantly less likely to report having had multiple sexual partners since graduating from Marine recruit training. The study found no statistically significant program impacts on the number of sexual partners for participants who were sexually experienced at baseline, or on consistency of condom use for any group of study participants.

The study also examined program impacts on measures of sexually transmitted infections and unintended pregnancies. Findings for these outcomes were not considered for this review because they did not meet the review evidence standards. Specifically, findings were reported only for certain subgroups of study participants, depending on where they were deployed after completing Marine recruit training. Those findings may be biased if deployment decisions were nonrandom.

Flinders 2013a

This study did not meet the review's eligibility criteria

Flinders 2013b

This study did not meet the review's screening criteria

Flinders 2013c

This study did not meet the review's eligibility criteria

Flinders 2013d

This study did not meet the review's screening criteria

Flinders et al. 2014

This study did not meet the review's screening criteria

Bernstein and Flinders 2017

This study did not meet the review's screening criteria

Flinders 2017

This study did not meet the review's eligibility criteria

Flinders and Zehler 2022

This study did not meet the review's screening criteria

Notes

Some study entries may include more than one citation because each citation examines a different follow-up period from the same study sample, or because each citation examines a different set of outcome measures on the same study sample. A blank cell indicates the study did not examine any outcome measures within the particular outcome domain or the findings for the outcome measures within that domain did not meet the review evidence standards.

Information on evidence of effectiveness is available only for studies that received a high or moderate rating. Read the description of the review process for more information on how these programs are identified.