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CompletedNCT00488202ANOVA1Updated Jun 1, 2017

Advanced Ovarian Cancer and Sexuality Phase 1

An observational study in Ovarian Cancer and Sexual Function, sponsored by University of British Columbia. Completed at 2 sites in Canada. Open to female participants aged 19 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-06-01.

Sponsored by University of British Columbia · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
26
Ages
19 Years to 65 Years
Sex
Female
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Study summary

Women with Advanced Ovarian Cancer (AOC) suffer from severe sexual side effects from treatment. The prevalence of the sexual issues is not known.

The degree to which these sexual side effects is affected by treatment is also not known, as the literature in this area focuses on post-treatment analysis.

Specific Aim #1 (Quantitative Phase): To determine the prevalence and types of sexual difficulties using self-report questionnaires in women about to receive treatment for Stage III or IV Ovarian Cancer at the BCCA and over time, and to correlate these symptoms with degree of cancer symptoms, well-being, depressive symptoms, and relationship satisfaction

Read the detailed description

Hypothesis 1a: Compared to baseline pre-treatment data, and to existing data for women with early-stage gynaecologic cancer, rates of sexual difficulties will be significantly higher and frequency of sexual intercourse will be significantly lower in women with advanced ovarian cancer. We hypothesize that difficulties specifically in the domains of sexual desire, sexual distress, and genital pain will be the most common types of sexual dysfunction to characterize women with advanced ovarian cancer.

Hypothesis 1b: We hypothesize that the degree of sexual symptoms will be significantly greater at 3 months and 10 months post-treatment than compared to pre-treatment, and that sexual difficulties may be significantly greater at 3 months post-treatment than at 10-months post-treatment.

Hypothesis 1c: We hypothesize that degree of sexual difficulty and sexual distress will be significantly correlated with (a) overall well-being; (b) depressive symptoms; and (c) relationship satisfaction.

Hypothesis 1d: As an exploratory analysis, we will investigate the relationship of ovarian cancer-related variables (i.e., type of treatment, duration of treatment, number of medications), and demographic variables (i.e., age, relationship duration, education) on each of the hypotheses in 1a - 1c.

02

Conditions studied

  • Ovarian Cancer
  • Sexual Function

Keywords

  • Advanced Ovarian Cancer
  • Sexual Function
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In context

Ovarian Neoplasms

2,695 studies on the registry are indexed under Ovarian Neoplasms; 727 are open to participants now.

This study's enrollment of 26 is below the median of 200 across 527 observational studies indexed under Ovarian Neoplasms.

Browse Ovarian Neoplasms studies →

Lead sponsor

University of British Columbia is the lead sponsor of 1,309 studies on the registry; 253 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 1 (17%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

women diagnosed with advanced ovarian cancer

Inclusion criteria

  • Women with Advanced Ovarian Cancer (AOC) who have not received treatment yet, but who are seeking treatment at the BC Cancer Agency.
  • Women must be able to understand English enough to fill out the questionnaire packages.
  • Mastery of written English is required. No translation services will be available for this study.

Exclusion criteria

Exclusion Criteria:

  • Anyone without an AOC diagnosis, who are not seeking treatment at BCCA, or who cannot understand enough English to complete the questionnaires will be excluded.
  • Those who do not have a mastery of written English are excluded.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
26 participants (actual)
06

Study locations

2 sites
  • UBC Sexual Health Lab, Vancouver Hospital
    Vancouver, British Columbia V5M 1M9, Canada
  • UBC Sexual Health Lab
    Vancouver, British Columbia V5Z 1M9, Canada
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 1, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00488202
Lead sponsor
University of British Columbia
Responsible party
Lori Brotto (Principal Investigator, University of British Columbia) — Principal investigator
First posted
Jun 20, 2007
Start date
May 2007
Primary completion
Aug 2011
Completion
Aug 2011
Last update
Jun 1, 2017

Study contacts

Lori A Brotto, PhD
principal investigator · UBC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2017. You cannot join it, but the record below documents what was studied.

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