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OpenTrials
Completed

NCT Number: NCT00883545

Study of Adherence to Colonoscopy in Women

The purpose of this study is to determine whether women who are offered screening colonoscopy will be more likely to schedule and complete this procedure if they are given the option of a woman endoscopist.

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Key information

Conditions

Age range

50 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Colorado Denver Health Sciences Center

Aurora, Colorado, 80045, United States

About this study

Colorectal cancer (CRC) is the third leading cause of cancer death in women. Although there are a variety of options for colon cancer screening, colonoscopy is thought to be the best modality for women. Despite recommendations by multiple societies, adherence to CRC screening among women is suboptimal. One possible barrier to adherence may be the gender of the endoscopist. Recent studies have shown that a large proportion of surveyed women would prefer a woman endoscopist. These studies suggest that having the option of a woman endoscopist would increase adherence to colonoscopy; however, there is no published literature that addresses this question.

Hypothesis

Women who are offered screening colonoscopy will be more likely to schedule and complete this procedure if they are given the option of a woman endoscopist.

Specific Aims

Primary

  • Determine whether the option of a woman endoscopist is associated with increased woman patient adherence to screening colonoscopy.
  • Assess the proportion of women who request a woman endoscopist when this option is made available to them.

Secondary

  • Identify socio-demographic predictors of (a) completing a screening colonoscopy and (b) requesting a woman endoscopist (e.g. race/ethnicity, age, health insurance, marital status).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female gender
  • Age between 50 and 70
  • Receiving primary care at a University Medicine clinic

Exclusion criteria

  • No visit to a University Medicine clinic in 18 months or more
  • Deceased
  • Pregnant
  • Terminal or cancer diagnosis
  • No longer receiving primary care at a University Medicine clinic

Treatment and study plan

Woman endoscopist

Other

This group will receive an invitation to schedule a screening colonoscopy with a woman endoscopist.

Usual Care

Other

This group will receive an invitation to schedule a screening colonoscopy with any available endoscopist.

Primary outcomes

  1. Determine whether the option of a woman endoscopist is associated with increased woman patient willingness to schedule and complete screening colonoscopy.

    Time frame: 6 months

Secondary outcomes

  1. Identify socio-demographic predictors of (a) completing a screening colonoscopy and (b) requesting a woman endoscopist (e.g. race/ethnicity, age, health insurance, marital status).

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Registry information

Official study title

The Effect of a Woman Endoscopist on Adherence to Screening Colonoscopy in Women

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Apr 17, 2009
Registry last updated
Jan 7, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.