Developing Rectal USPE Measures

NCT ID: NCT02102867

Last Updated: 2026-02-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-04-30
• Study Completion Date: 2022-04-01

Brief Summary

The purpose of this study is to: (a) adapt existing vaginal USPE items/instruments for evaluation of similar elements of rectal compartment use; (b) develop these scales using 3 distinct semi-solid formulations that represent a range of physicochemical and rheological properties of microbicides that are currently being designed for dual compartment use; and (c) develop novel USPE instruments to capture the experience of product use in the context of receptive anal intercourse (RAI) in both male and female cohorts.

Detailed Description

HIV prevention is a global public health priority. Providing efficacious prevention methods that have the greatest likelihood of use will have a profound impact on the public's health. Critical to their use is "acceptability." However, current conceptualizations of adherence and acceptability fail to fully articulate and account for patterns of use and non-use. Formulation properties are critically important to both drug delivery and the user experience. Microbicide developers thus have the opportunity to directly control a formulation's impact on acceptability and adherence to product use, as well as biological product performance. Microbicide products can and should be developed such that they achieve performance standards for both these behavioral (user experience) and biological (efficacy) functions. By incorporating the user experience early on in the product development process, developers will have the greatest chance of providing at-risk individuals with the best prevention methods science can provide. Developing prevention products that can be used in the vagina and/or the rectum and that optimize the user experience in both compartments increases the likelihood that these products will be used consistently and correctly. The impact on global public health has the potential to be far-reaching, decreasing HIV and sexually transmitted infections (STI) incidence and prevalence in both women and men.

Methodology and Data Collection: This is a formative study in which volunteers (N~20-30; ~8-20 males; ~8-20 Females) will first be prescreened for basic study eligibility using a brief questionnaire. Those who are interested in the study and are eligible based on their responses to the prescreen will then complete a STI/HIV screening and pregnancy test (for females).

During the course of the study, participants will evaluate 3 study products (i.e., distinct semi-solid formulations that represent a range of physicochemical and rheological properties). Each participant will be randomly assigned to the order in which they will evaluate the 3 products. After a sexual encounter that includes RAI and study product use, participants will be required to complete a web survey about their experience with the study product.

Conditions

Microbicide Delivery System Perceptibility and Acceptability

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Formulations

Gel, Cream, Liquid

Group Type: OTHER

Gel

Intervention Type: OTHER

10mL

Cream

Intervention Type: OTHER

10mL

Liquid

Intervention Type: OTHER

10mL

Interventions

Gel

10mL

Intervention Type: OTHER

Cream

10mL

Intervention Type: OTHER

Liquid

10mL

Intervention Type: OTHER

Other Intervention Names

Orange; Green; Yellow

Eligibility Criteria

Inclusion Criteria

• Eligible male participants must be 18 years of age or older
• Eligible female participants must be 18-45 years of age

• Report receptive anal intercourse (RAI) at least twice in the past 6 months,
• Are willing to use each study product in conjunction with RAI on at least one occasion in each data collection period (resulting in a minimum of 3 RAI events during each product evaluation period; on average every 2 weeks, all 3 products across an average of 6 -12 weeks))
• Are willing and able to respond to study data collection systems via phone and internet, attend all study visits, and participate in in-depth qualitative interviews

Exclusion Criteria

• Male and female participants will be ineligible if they:

• Have a sensitivity or allergy to vaginal, anal, or rectal products,
• Have a sensitivity or allergy to any of the ingredients contained in the study products,
• Are HIV positive at baseline, or have a known HIV-positive sexual partner,
• Have an active rectal or reproductive tract infection requiring treatment per current Centers for Disease Control (CDC) guidelines or symptomatic urinary tract infection (UTI). Infections requiring treatment include Chlamydia (CT)*, gonorrhea (GC)*, syphilis, active herpes simplex virus (HSV) lesions (note: HSV seropositivity with no active genital lesions is not an exclusion criterion, since treatment is not required), chancroid, genital sores or ulcers, and, if clinically indicated, genital warts,
• Have current inflammatory bowel disease (IBD) or history of active IBD within last 3 months,
• Have any other significant colorectal symptom(s) as determined by medical history, participant self-report , or physical exam (including but not limited to presence of any unresolved injury, infectious or inflammatory condition of the local mucosa, presence of symptomatic external hemorrhoids, and presence of any painful anorectal conditions that would be tender to manipulation),
• Have a nontreatable sexually transmitted disease that could, in the opinion of the investigator/study clinician, make the patient unsuitable for the study or unable to comply with study requirements
• Have any other clinical condition or prior therapy that, in the opinion of the investigator/study clinician, would make the patient unsuitable for the study or unable to comply with the study requirements,
• Are unwilling to refrain from use of nonoxynol-9 (N9) for the duration of the study,
• Are unable or unwilling to communicate in English, or
• Are unable or unwilling to give written informed consent.

Additionally, female participants will be ineligible if they:

• Are pregnant or breastfeeding.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

ImQuest Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: collaborator

The Miriam Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kathleen Morrow, PhD

Role: PRINCIPAL_INVESTIGATOR

The Miriam Hospital: Centers for Behavioral & Preventive Medicine

Robert Buckheit, PhD

Role: PRINCIPAL_INVESTIGATOR

ImQuest Pharmaceuticals, Inc.

Locations

The Miriam Hospital: Centers for Behavioral & Preventive Medicine

Providence, Rhode Island, United States

Countries

United States

Other Identifiers

U19AI101961

Identifier Type: NIH

Identifier Source: secondary_id

View Link

11968

Identifier Type: -

Identifier Source: org_study_id