Speculum Insertion Study

Sponsor
Unity Health Toronto (Other)
Overall Status
Unknown status
CT.gov ID
NCT02708615
Collaborator
(none)
304
1
2
74
4.1

Study Details

Study Description

Brief Summary

This study compares two different types of speculum insertion to determine the level of discomfort they might cause. This study compares the straight horizontal insertion (SHI) of the speculum and the vertical insertion and rotation (VIR).

Participants are randomly assigned to one of the two insertion groups and are not told which group they are in until the examination is over. Participants rate their level of discomfort immediately after insertion of the speculum.

Basic demographic information (e.g., age, ethnicity, number of vaginal deliveries, menopausal status, etc.) and clinical information are also collected to determine if other factors influence the level of discomfort experienced.

NOTE This is NOT a paid study.

Condition or Disease Intervention/Treatment Phase
  • Other: Type of speculum vaginal insertion method
N/A

Detailed Description

In most medical schools around the world, speculum examination is taught using a bivalved speculum, since this is the type of speculum most commonly used in clinical practice. Due to the oval shape of the vulva, and the alignment of the labia majora and minora, the aperture of vaginal introitus is commonly perceived to have a vertical orientation. In reality however, the vaginal introitus is round and the vagina itself has more of a horizontal orientation: the anterior and posterior vaginal walls are opposed, and the sidewalls only become apparent once the anterior and posterior walls are separated. Nevertheless, the most common way of teaching the speculum examination worldwide is to introduce the speculum in a vertical orientation and then once it is successfully inserted into the vagina to rotate it 90° into a horizontal position. Once it is correctly positioned, it is slowly opened to visualize the vaginal epithelium and the cervix. However, in clinical practice, the rotation of the speculum in the vagina may cause pain and discomfort. Introduction of the speculum initially in a horizontal orientation, without rotation in the vagina, seems more appropriate and could potentially be associated with less discomfort or pain for women undergoing this exam. In practice, a minority of clinicians separate the labia first, introduce the speculum in a direct horizontal fashion, and thus avoid the potentially uncomfortable twisting part of the procedure.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
304 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
A Randomized Controlled Trial of Gynecological Speculum Examination: Straight Horizontal Insertion vs. Vertical Insertion and Rotation
Actual Study Start Date :
Nov 1, 2015
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Vertical rotation

Vertical insertion and 90 degree rotation of speculum in vagina

Other: Type of speculum vaginal insertion method
Speculum insertion type will either be vertical rotation (as per common practice in Canada) or straight horizontal insertion

Other: Straight horizontal insertion

Straight horizontal insertion of speculum with no rotation in vagina

Other: Type of speculum vaginal insertion method
Speculum insertion type will either be vertical rotation (as per common practice in Canada) or straight horizontal insertion

Outcome Measures

Primary Outcome Measures

  1. Pain/discomfort ratings of women receiving straight horizontal speculum insertion vs. those receiving vertical speculum insertion and rotation, as measured by a visual analog scale [Measured immediately after speculum insertion]

    The primary objective of this study is to quantify the amount of pain/discomfort women experience with two different types of speculum insertion: straight horizontal insertion (SHI) and vertical insertion and rotation (VIR). Participants will rate their pain/discomfort by placing a mark on a visual analog scale measuring 10 cm in length. Pain/discomfort ratings on this scale range from "no pain" to "pain as bad as it possibly could be".

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Women who are 18 years of age or older

  • Undergoing a speculum examination as part of their regular clinical care

  • Proficient knowledge of the English language and able to sign the informed consent form

Exclusion Criteria:
  • Younger than 18 years of age

  • Women with a history of vulvodynia, vaginismus, or dyspareunia

  • No prior sexual activity or intercourse

  • Active vaginal, cervical, uterine or adnexal infection

  • Active pregnancy or within 6 weeks postpartum

  • Vulvar or vaginal surgery within three months

  • Psychiatric conditions

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Michael's Hospital Toronto Ontario Canada M5B 1W8

Sponsors and Collaborators

  • Unity Health Toronto

Investigators

  • Principal Investigator: Michael Geary, MD, Unity Health Toronto

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Unity Health Toronto
ClinicalTrials.gov Identifier:
NCT02708615
Other Study ID Numbers:
  • 15-082
First Posted:
Mar 15, 2016
Last Update Posted:
Apr 29, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No

Study Results

No Results Posted as of Apr 29, 2020