SiHLE - 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
Ralph DiClemente, Ph.D., Gina Wingood, Sc.D. M.P.H., Kathy Harrington, Delia Lang, Susan Davies, Edward Hook III, M. Kim Oh, Richard Crosby, Ph.D., Vicki Stover Hertzberg, Angelita Gordon, James Hardin, Ph.D., Shan Parker, and Alyssa Robillard.
Program Summary

SiHLE - Sisters, Informing, Healing, Living, Empowering - is a peer-led, group-level, social-skills training intervention designed to reduce sexual risk behaviors among African-American female teenagers who are at high risk of HIV. In addition to HIV prevention, the program addresses relationships, dating, and sexual health within the specific context of the female African-American teenage experience. The program draws upon both cultural and gender pride to give participants the skills and motivations to avoid HIV and other STDs.

Intended Population
The target population is heterosexual African-American females between the ages of 14 and 18 who have had sexual intercourse and are at risk for HIV. The program was evaluated with patients at community health agencies.
Program Setting

The program was designed for and evaluated in community-based organizations and health clinics.

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-sihle-health-workshops-for-young-black-women

Currently no formal training offered

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)

Sociometrics offers the evaluation instruments used in the original implementation of the program and the Prevention Minimum Evaluation Data Set, a generic questionnaire that can be adapted to suit most prevention programs.

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 dosage itself is described in the Notes when available.

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.

For more details about program components, refer to the FAQ page.

Category Component Core Component Component present Lesson number(s) / activities where present
Delivery mechanism Other
Dosage Frequency Yes Yes
Dosage Intensity Yes Yes
Dosage Duration Yes Yes
Dosage Other
Staffing Deliverer: Community health worker No
Staffing Deliverer: Faith-based individual No
Staffing Deliverer: Health educator No
Staffing Deliverer: Mental health provider No
Staffing Deliverer: Mentors No
Staffing Deliverer: Parents/family No
Staffing Deliverer: Peers Yes Yes (both versions) Sessions 1,2,3, and 4
Staffing Deliverer: Primary care provider No
Staffing Deliverer: Social worker and/or counselor Yes Yes (both versions) Session 1,2,3 and 4
Staffing Deliverer: Teachers No
Staffing Deliverer: Other No
Staffing Experience: Credentials No
Staffing Experience: Education No Yes (both versions)
Staffing Experience: Other No
Staffing Number of staff providing services No Yes (both versions)
Staffing Training: Additional training required No
Staffing Training: Developer-led training required No Yes (both versions)
Staffing Training: Other No
Staffing Other No
Format Group size: Full-group activity No
Format Group size: Independent/individual activity No
Format Group size: Small-group activity No
Format Group size: Other No Yes (both versions)
Format Mode: In-person No Yes (both versions)
Format Mode: Phone (audio) No
Format Mode: Phone (text) No
Format Mode: Phone (app) No
Format Mode: Online/computer (asynchronous) No
Format Mode: Online/computer (synchronous) No
Format Mode: Other No
Format Other No
Context Context: Environmental supports No Yes (both versions)
Context Context: Environmental constraints No
Context Context: Other No
Context Setting: After school No
Context Setting: Community based No Yes (both versions)
Context Setting: Correctional facility No
Context Setting: Faith based No
Context Setting: Health care clinic No Yes (both versions)
Context Setting: Home-based case management No
Context Setting: Home/housing No
Context Setting: In school (during the school day) No
Context Setting: Mental health clinic No
Context Setting: Residential facility No
Context Setting: School-based health clinic No
Program Objectives
The goal of the SiHLE program is to teach social skills to reduce risky sexual behaviors among participants. The program seeks to increase assertive communication skills, condom use skills, and self-efficacy.  
Program Content
The four SiHLE sessions focus on educating teens on HIV transmission and risk reduction strategies by: 
  • Developing assertive communication skills to demonstrate care for their partners and to negotiate abstinence or safer sex behaviors (particularly condom use and involvement of partners in decision-making)
  • Building proper condom use skills (including learning how to place a condom on a partner) and positive attitudes, norms and self-efficacy about consistent condom use
  • Understanding of characteristics of healthy and unhealthy relationships and the triggers that make negotiating safer sex challenging for teens, and
  • Empowerment and self-efficacy, based on cultural and gender pride
Program Methods
The program is delivered by one facilitator and two peer mentors through group discussion, role play, activities, and games. Review of previous information is built in throughout the sessions to reinforce knowledge and offer opportunities for questions to be answered.
Program Structure and Timeline

The program is delivered in four sessions that are each four hours long. The ideal group size is 10 to 12 participants with one adult and two peer facilitators.

The program must be delivered in community-based settings, not in school or during school hours.

Staffing

The program requires the use of one adult and two peer facilitators, all of whom should be African American and female. Peer facilitators should be between 18- and 21-years-old who, ideally, have gone through the SiHLE program. There are specific roles for the adult and peer facilitators described in the facilitator's manual.

Staff Training
There is no required training for this program. In the past several organizations have offered formal training, but none are currently specified.
Program Materials and Resources

The following program materials are available through the distributor:

  • User's Guide
  • SiHLE Facilitators Manual
  • Photocopy masters of posters
  • Participant Handbook
  • Photocopy masters of additional handouts, the SiHLE Jeopardy game, session evaluations
  • 50 Domestic violence brochures
  • Prevention Minimum Evaluation Data Set (PMEDS)
  • Local Evaluator Consultant Network Directory
  • Original Evaluation Instruments

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
Delivery of the program requires the use of condoms and penis models.
Fidelity
SiHLE has a fidelity toolkit/checklist and tools for monitoring program implementation. These may be accessed on the Sociometrics website: https://www.socio.com/products/pasha-sihle-health-workshops-for-young-black-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
All adaptations must be approved by the developer, in consultation with Sociometrics.
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

DiClemente et al. 2004

Wingood et al. 2006

Sales et al. 2010

DiClemente et al. 2010

Klein and Card 2011

Danielson et al. 2013

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

DiClemente et al. 2004

Wingood et al. 2006

Sales et al. 2010

After school 14 to 17 African American or Black Young female

522

DiClemente et al. 2010

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

Klein and Card 2011

After school 14 to 17 African American or Black Young female

178

Danielson et al. 2013

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

DiClemente et al. 2004

Wingood et al. 2006

Sales et al. 2010

n.a. Potentially favorable evidence Favorable evidence Potentially favorable evidence Potentially favorable evidence

DiClemente et al. 2010

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

Klein and Card 2011

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

Danielson et al. 2013

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

DiClemente et al. 2004

Wingood et al. 2006

Sales et al. 2010

The program's evidence of effectiveness was first established in a randomized controlled trial involving sexually active African American females recruited from four community health agencies in the southern United States. Study participants were randomly assigned to either a treatment group that received the intervention or a control group that received a general health promotion intervention on nutrition and exercise. Surveys were administered immediately before the intervention and at follow- ups conducted 6 and 12 months after the intervention. Biological testing for chlamydia, gonorrhea, and trichomonas was also conducted.

The study found that six months after the intervention, adolescents participating in the intervention were significantly less likely to report having a pregnancy and significantly more likely to report consistent condom use in the past 6 months. Adolescents participating in the intervention were significantly more likely to report having used a condom during last sex, reported a significantly higher percentage of condom-protected sexual intercourse acts during both the past 30 days and the past 6 months, were less likely to have had a new vaginal sex partner in the last 30 days, and reported significantly fewer episodes of unprotected sexual intercourse during both the past 30 days and the past 6 months. The study found no statistically significant impacts on self-reported condom use in the past 30 days.

The study found that twelve months after the intervention, adolescents participating in the intervention were significantly more likely to report consistent condom use in the both the past 30 days and the past 6 months. Adolescents participating in the intervention were significantly more likely to report using a condom during last sex, reported a significantly higher percentage of condom-protected sexual intercourse acts during both the past 30 days and the past 6 months, and reported significantly fewer episodes of unprotected sexual intercourse during both the past 30 days and the past 6 months. The study found no statistically significant program impacts on self-reported pregnancy in the past 6 months.

During the 12-month follow-up period, adolescents participating in the intervention were significantly less likely to have a chlamydia infection. The study found no statistically significant program impacts on gonorrhea or trichomonas infections.

DiClemente et al. 2010

Klein and Card 2011

This study evaluated an adapted version of the SiHLE program with a randomized controlled trial involving African American female adolescents in the San Francisco Bay Area. The adapted "Multimedia" version of the program comprised two one-hour sessions delivered individually by computer. Study participants were randomly assigned to either a treatment group that received the intervention or to a control group that received a general health education session. Surveys were administered immediately before random assignment (baseline) and three months after baseline.The study examined changes in rates of sexual risk behaviors between the baseline and three-month follow-up surveys. However, the study did not test for differences in these outcomes between the treatment and control groups. The study also examined measures of condom-use self-efficacy, knowledge, sexual-communication self-efficacy. Findings for these outcomes were not considered for the review because they fell outside the review of the review.

Danielson et al. 2013

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.

Language directly from the program model developer or authors.