Evaluating the Human Papillomavirus Self-Collection Experience in Individuals Who Have Experienced Sexual Trauma

Sponsor
OHSU Knight Cancer Institute (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05458869
Collaborator
Oregon Health and Science University (Other), Robert Wood Johnson Foundation (Other)
15
1
13
1.2

Study Details

Study Description

Brief Summary

This study explores the human papillomavirus (HPV) self-collection experience among individuals with a history of sexual trauma. Cervical cancer is the fourth most common cancer in women worldwide and is the second leading cause of cancer-related death in women ages 29-39. Despite programs to improve accessibility of cervical cancer screening and overall high screening rates, disparities in routine surveillance have been demonstrated in certain populations, such as victims of intimate partner violence and sexual trauma. One barrier to participating in cervical cancer screening for this population is the office-based visit which necessitates the individual to undress, sit with their legs in stirrups, and undergo speculum examination for specimen collection. This type of visit may cause distress for participants who have experienced sexual violence. HPV self-collection has been studied with favorable outcomes in effectiveness and ease of use. This study evaluates the experience of HPV self-collection among individuals who have experienced sexual trauma.

Condition or Disease Intervention/Treatment Phase
  • Procedure: HPV Self-Collection
  • Other: Interview
  • Other: Survey Administration

Detailed Description

PRIMARY OBJECTIVE:
  1. To explore the HPV self-collection experience among individuals with a history of sexual trauma.
OUTLINE:

Participants complete a survey, use an HPV self-collection kit, and attend an interview over 30 minutes.

Study Design

Study Type:
Observational
Anticipated Enrollment :
15 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Qualitative Study of HPV Self-Collection Experience and Cervical Cancer Screening in Patients With a History of Sexual Trauma
Anticipated Study Start Date :
Aug 31, 2022
Anticipated Primary Completion Date :
Aug 31, 2023
Anticipated Study Completion Date :
Sep 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Observational (survey, HPV self-collection, interview)

Participants complete a survey, use an HPV self-collection kit, and attend an interview over 30 minutes.

Procedure: HPV Self-Collection
Use HPV self-collection kit
Other Names:
  • At-home HPV Self Collection
  • HPV Self Collection
  • Human Papillomavirus Self-Collection
  • Other: Interview
    Attend interview

    Other: Survey Administration
    Complete surveys

    Outcome Measures

    Primary Outcome Measures

    1. Experience of cervical cancer screening in patients with a history of sexual trauma [Up to 12 months]

      Data analysis of interview transcripts will occur concurrent with data collection. The transcripts will be analyzed using Taguette, a qualitative software program. The coding scheme to analyze interview transcripts will be developed through an iterative and reflective process using grounded theory. A comparative, iterative, and interactive method, grounded theory follows a cyclical research process of collecting, analyzing and coding data, memo-writing and theoretical sampling to the point of saturation, where no new ideas, theories or constructs emerge. The research team will thoroughly explore the data and develop a comprehensive list of categories. The categories will be used to identify themes and make connections both between and across interview subjects. Thematic analysis will be basis of the study's findings.

    2. Utility of HPV self-collection among patients with a history of sexual trauma [Up to 12 months]

      Data analysis of interview transcripts will occur concurrent with data collection. The transcripts will be analyzed using Taguette, a qualitative software program. The coding scheme to analyze interview transcripts will be developed through an iterative and reflective process using grounded theory. A comparative, iterative, and interactive method, grounded theory follows a cyclical research process of collecting, analyzing and coding data, memo-writing and theoretical sampling to the point of saturation, where no new ideas, theories or constructs emerge. The research team will thoroughly explore the data and develop a comprehensive list of categories. The categories will be used to identify themes and make connections both between and across interview subjects. Thematic analysis will be basis of the study's findings.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Individuals with a cervix who are eligible for primary HPV testing (age 25 and older) according to national cervical cancer screening guidelines

    • Identify themselves as having a history of IPV, sexual abuse, or sexual trauma

    • Participants will also need to have access to a smartphone, tablet, or computer with video capability

    • English speaking

    • Reside in the State of Oregon

    • Patients who have participated in prior HPV self-collection study (reference Institutional Review Board [IRB] number- IRB# 23478) will also be eligible to participate in the interview if they meet the remaining eligibility requirements (i.e. history of IPV, sexual abuse, sexual trauma)

    Exclusion Criteria:
    • Individuals who are not English speaking

    • Individuals < 25 years old or no longer eligible/recommended to undergo cervical cancer screening

    • Resides outside the state of Oregon

    • Adults who are unable to consent or are decisionally impaired

    • Individuals without a cervix (i.e. prior hysterectomy)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 OHSU Knight Cancer Institute Portland Oregon United States 97239

    Sponsors and Collaborators

    • OHSU Knight Cancer Institute
    • Oregon Health and Science University
    • Robert Wood Johnson Foundation

    Investigators

    • Principal Investigator: Amanda S Bruegl, OHSU Knight Cancer Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Amanda Bruegl, MD, Principal Investigator, OHSU Knight Cancer Institute
    ClinicalTrials.gov Identifier:
    NCT05458869
    Other Study ID Numbers:
    • STUDY00024429
    • NCI-2022-05454
    • STUDY00024429
    First Posted:
    Jul 14, 2022
    Last Update Posted:
    Jul 14, 2022
    Last Verified:
    Jul 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 14, 2022