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The Feasibility of Self or Partner-assisted Digital Anal Exam Screening

Primary Purpose

Anus Neoplasms

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-anal exam arm
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Anus Neoplasms

Eligibility Criteria

27 Years - 80 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Men who are aged 27-80 years
  • Acknowledge sex with men in their lifetime
  • Reside in Harris County, Texas
  • Understand and speak English.

Exclusion Criteria:

  • Current doctor's diagnosis of anal condyloma, hemorrhoids, fissures, or anal cancer

Sites / Locations

  • University of Texas School of Public Health

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Self-anal exam arm

Arm Description

Study only has one arm.

Outcomes

Primary Outcome Measures

Kappa agreement will be calculated between lay person and nurse practitioner on the anal exam results.

Secondary Outcome Measures

Odds ratios will be calculated for the association between partnership status and concordance between participant and clinician.
Odds ratios will be calculated for the association between age and concordance between participant and clinician.
Odds ratios will be calculated for the association between waist circumference and concordance between participant and clinician.
Odds ratios will be calculated for the association between race and concordance between participant and clinician.
Odds ratios will be calculated for the association between ethnicity and concordance between participant and clinician.
Number of persons who state that a self-DAE is an acceptable procedure.
Number of persons with adverse events after conducting a self-DAE.
Number of persons who state they have the ability to conduct a self-DAE.
Number of persons who state they intend to seek subsequent care in the event of an abnormal result to a self-DAE.

Full Information

First Posted
March 3, 2015
Last Updated
May 10, 2016
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Cancer Institute (NCI), Baylor College of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02384005
Brief Title
The Feasibility of Self or Partner-assisted Digital Anal Exam Screening
Official Title
The Feasibility of Self or Partner-assisted Digital Anal Exam Screening
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
February 2015 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Cancer Institute (NCI), Baylor College of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is no standard screening protocol for anal cancer even as disease incidence increases. This single-visit study will clarify if single persons can do a self-digital anal exam, or perhaps the exam requires a partner, or if, in fact, the exam requires a clinician for reasons of safety, accuracy, or acceptability. The investigators hypothesize that men having sex with men's digital anal exam (DAE) findings will have moderate or substantial agreement with a nurse practitioner DAE for detecting an anal abnormality (defined as condylomas, hemorrhoids, fissures, and malignant tumors). As a secondary hypothesis the investigator believe a partner-assisted DAE conducted within a couple will have better agreement with the nurse practitioner DAE than will a self-DAE conducted by a single person.
Detailed Description
There is no standard screening protocol for anal cancer even as disease incidence and mortality increases; however, a digital anorectal exam (also called a digital rectal exam) will play a role in any recommended protocol. Critically, fewer digital anorectal exams are being performed by physicians even though it is a simple and quick procedure. If men who have sex with men (MSM) can learn to examine the anal canal, then detection and treatment of early cancers among this population may increase. This single-visit Phase II feasibility study will investigate increasing digital anal exam (DAE) use to enhance screening for anal cancer among MSM aged 27-80 years. The investigators hypothesize that MSM's DAE findings will have moderate or substantial agreement with a nurse practitioner DAE for detecting an anal abnormality (defined as condylomas, hemorrhoids, fissures, and malignant tumors). As a secondary hypothesis the investigators believe a partner-assisted DAE conducted within a couple will have better agreement with the nurse practitioner DAE than will a self-DAE conducted by a single person. It is not proposed that lay persons recognize specific conditions but, rather, that any abnormality should trigger a doctor visit. The specific aims are: Estimate the agreement between the digital anal exams of 200 MSM and the gold standard of a highly experienced nurse practitioner during a single clinical visit. This aim will answer the question: under optimal circumstances, will MSM report accurate findings after performing their own DAE? Determine factors independently associated with concordance of MSM and nurse practitioner DAEs including age, single men vs. men in couples, race, ethnicity and waist circumference. This aim will provide insight into which MSM are more likely to perform accurate DAEs. Assess DAE acceptability, self-efficacy, safety, and intentions-to-seek subsequent care. This aim will answer the question: will lay-performed DAEs have sufficient acceptability and safety and trigger appropriate follow-up care? The goal is to advance knowledge of how to increase use of digital anal exams to reduce anal cancer morbidity and mortality. The study will clarify if single persons can do a self-digital anal exam, or perhaps the exam requires a partner, or if, in fact, the exam requires a clinician for reasons of safety, accuracy, or acceptability.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anus Neoplasms

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
201 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-anal exam arm
Arm Type
Other
Arm Description
Study only has one arm.
Intervention Type
Other
Intervention Name(s)
Self-anal exam arm
Intervention Description
After a short pre-test the clinician will use a model to show a normal and diseased anal canal and then use pictures to show a self-DAE. The clinician will describe how to do a self-DAE for single men and partners. Next, the clinician will ask the participant to lower his pants for collection of anal human papillomavirus (HPV) DNA and cytology. The clinician will conduct a DAE and then participants will do self-DAE done in private. Then the research assistant will demonstrate the computer-assisted self-interview. When participants return to the clinician to receive the DAE results, the clinician will conduct a safety-related interview. The clinician will treat external anal disease, triage internal anal disease, and ask to be notified if a participant has any anus-related concerns in the following week. A complete appointment will require 70 minutes for singles and 105 minutes for couples. The PI will later conduct 3 focus groups.
Primary Outcome Measure Information:
Title
Kappa agreement will be calculated between lay person and nurse practitioner on the anal exam results.
Time Frame
This cross-sectional design measures agreement on Day 1.
Secondary Outcome Measure Information:
Title
Odds ratios will be calculated for the association between partnership status and concordance between participant and clinician.
Time Frame
This cross-sectional design collects data for the odds ratios on Day 1
Title
Odds ratios will be calculated for the association between age and concordance between participant and clinician.
Time Frame
This cross-sectional design collects data for the odds ratios on Day 1
Title
Odds ratios will be calculated for the association between waist circumference and concordance between participant and clinician.
Time Frame
This cross-sectional design collects data for the odds ratios on Day 1
Title
Odds ratios will be calculated for the association between race and concordance between participant and clinician.
Time Frame
This cross-sectional design collects data for the odds ratios on Day 1
Title
Odds ratios will be calculated for the association between ethnicity and concordance between participant and clinician.
Time Frame
This cross-sectional design collects data for the odds ratios on Day 1
Title
Number of persons who state that a self-DAE is an acceptable procedure.
Time Frame
This cross-sectional design collects these data on Day 1
Title
Number of persons with adverse events after conducting a self-DAE.
Time Frame
This cross-sectional design collects these data on Day 1
Title
Number of persons who state they have the ability to conduct a self-DAE.
Time Frame
This cross-sectional design collects these data on Day 1
Title
Number of persons who state they intend to seek subsequent care in the event of an abnormal result to a self-DAE.
Time Frame
This cross-sectional design collects these data on Day 1

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
27 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men who are aged 27-80 years Acknowledge sex with men in their lifetime Reside in Harris County, Texas Understand and speak English. Exclusion Criteria: Current doctor's diagnosis of anal condyloma, hemorrhoids, fissures, or anal cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan G. Nyitray, PhD
Organizational Affiliation
University of Texas School of Public Health at Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas School of Public Health
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
28835533
Citation
Nyitray AG, Hicks JT, Hwang LY, Baraniuk S, White M, Millas S, Onwuka N, Zhang X, Brown EL, Ross MW, Chiao EY. A phase II clinical study to assess the feasibility of self and partner anal examinations to detect anal canal abnormalities including anal cancer. Sex Transm Infect. 2018 Mar;94(2):124-130. doi: 10.1136/sextrans-2017-053283. Epub 2017 Aug 23.
Results Reference
derived

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The Feasibility of Self or Partner-assisted Digital Anal Exam Screening

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