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CompletedNCT04840329Updated Feb 21, 2023

Endocation: Trial of an Endometriosis Education Program

An interventional study of Education in Endometriosis, sponsored by BC Women's Hospital & Health Centre. Completed at 1 site in Canada. Per ClinicalTrials.gov, last updated 2023-02-21.

Sponsored by BC Women's Hospital & Health Centre · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
67
Allocation
Randomized
Sex
All
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Study summary

Endometriosis is a common condition that affects 10% of females, causing chronic pain and other health concerns. Currently, it takes 8-12 years to be diagnosed with endometriosis, in part because there is low awareness of this condition. This research is designed to test whether providing endometriosis education in schools can help increase early awareness of the condition.

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Conditions studied

  • Endometriosis

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03

In context

Endometriosis

920 studies on the registry are indexed under Endometriosis; 266 are open to participants now.

This study's enrollment of 67 is close to the median of 67 across 540 interventional studies indexed under Endometriosis.

Browse Endometriosis studies →

Lead sponsor

BC Women's Hospital & Health Centre is the lead sponsor of 11 studies on the registry; 2 are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 8-12 grade level class

Exclusion criteria

Exclusion Criteria:

  • Instruction offered in a language other than English
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
67 participants (actual)

Study arms

  • Experimental
    Education Arm

    Behavioral: Education

  • No intervention
    Waitlist Control Arm

Interventions

  • BehavioralEducation

    One-time educational session about menstrual health and endometriosis

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What researchers measure

Primary outcomes

  1. Change from baseline in menstrual health and endometriosis knowledge

    Assessed using a built for purpose questionnaire, possible scores range from 0 to 8

    Time frame: Baseline and 4 weeks

Secondary outcomes

  1. Change from baseline in prioritization of menstrual health

    Assessed using a built for purpose item, possible scores range from 0 to 4

    Time frame: Baseline and 4 weeks

  2. Change from baseline in confidence in endometriosis knowledge

    Assessed using a built for purpose item, possible scores range from 0 to 4

    Time frame: Baseline and 4 weeks

  3. Change from baseline in comfort with menstrual health

    Assessed using a built for purpose item, possible scores range from 0 to 4

    Time frame: Baseline and 4 weeks

  4. Acceptability of menstrual health and endometriosis education (quantitative)

    Assessed using a built for purpose questionnaire, possible scores range from 0 to 35

    Time frame: Immediately following education in intervention and waitlist control group

  5. Acceptability of menstrual health and endometriosis education (qualitative)

    Assessed using open-ended responses a built for purpose questionnaire

    Time frame: Immediately following education in intervention and waitlist control group

  6. Refusal of participants invited to participate

    Number of participants who refuse to participate divided by the number of participants invited to participate

    Time frame: Baseline

  7. Retention of participants

    Number of participants completing the study divided by the number of participants enrolled

    Time frame: 4 weeks

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Study locations

1 site
  • BC Women's Hospital
    Vancouver, British Columbia V6H 3N1, Canada
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2021 to primary completion in May 2021, 1 month.

Of 196 non-industry interventional studies with no phase under Endometriosis, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 44. This study's 1 month is below that.

Counting every sponsor, half of 211 studies reached it within 25 months; a quarter within 13 and three quarters within 44.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 7, 2021
First posted
Apr 12, 2021
StartActual
Apr 9, 2021
Primary completionActual
May 20, 2021
CompletionActual
May 20, 2021
Last update
Feb 21, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 21, 2023, 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
NCT04840329
Lead sponsor
BC Women's Hospital & Health Centre
Collaborators
BC Support Unit
Responsible party
Paul Yong (Associate Professor, BC Women's Hospital & Health Centre) — Principal investigator
First posted
Apr 12, 2021
Start date
Apr 9, 2021
Primary completion
May 20, 2021
Completion
May 20, 2021
Last update
Feb 21, 2023

Study contacts

Paul Yong
principal investigator · University of British Columbia

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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