NCT07524764

Brief Summary

This is a mixed-method study aimed at gathering new evidence on reproductive health among female service members in the Canadian Armed Forces (CAF). Reproductive health includes four primary domains: contraception; undesired reproductive outcomes (including unintended pregnancy, adverse pregnancy outcomes, and infertility); assisted reproductive care; and pelvic floor dysfunctions. Additional factors that may influence reproductive outcomes will also be explored, including gynecological health (including but not limited to menstrual health, menopause, breast injury, sexually transmitted and blood-borne infections) as well as physical and psychological health (including but not limited to repetitive strain injuries, depression, and post-traumatic stress disorder). Evidence gathered on reproductive health issues will include, but not limited to, the lived experiences (occurrence), associated risk factors, access to care, including barriers and facilitators, service utilization, and career-related impacts among actively serving members and Veterans of the CAF. These will inform the development of recommendations and support services aimed at improving reproductive health care within the CAF. This project is divided into 3 convergent parts: Part 1: An online pan-Canadian survey that will achieve a minimum total sample of 1067 participants. Part 2: Semi-structured individual interviews (open-ended questions) will be conducted with female CAF members and Veterans who have experienced at least one reproductive health issues. A total of 30 participants are estimated to be required to achieve data saturation across the four primary domains. Part 3: Semi-structured group discussion (open-ended questions) will be conducted with healthcare providers, who have experience with treating female reproductive health issues in CAF members, as well as stakeholders and policymakers involved in supporting female members of the CAF/Veterans. A total of 24 healthcare providers/stakeholders/policymakers will form 3 group discussion (8 participants/group). For all 3 parts, efforts in recruitment will be made to ensure representation across CAF elements, minority groups, and native language (French and English).

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,121

participants targeted

Target at P75+ for all trials

Timeline
8mo left

Started Apr 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Apr 2026Dec 2026

First Submitted

Initial submission to the registry

April 1, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

April 15, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2026

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

8 months

First QC Date

April 1, 2026

Last Update Submit

April 8, 2026

Conditions

Keywords

Reproductive health issueWomen's healthPregnancyInfertilityPelvic floor dysfunctionContraceptionCanadian Armed ForcesMilitary personnel

Outcome Measures

Primary Outcomes (8)

  • Occurrence of female reproductive health issues

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options

    Baseline

  • Lived experiences of female reproductive health issues

    Assessed using semi-structured individual interviews with open-ended questions

    Baseline

  • Risk factors of reproductive health issues

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions

    Baseline

  • Barriers to access to care for reproductive health issues

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions and group discussion (open-ended questions) with healthcare providers, stakeholders and policymakers

    Baseline

  • Facilitators to access to care for reproductive health issues

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions and group discussion (open-ended questions) with healthcare providers, stakeholders and policymakers

    Baseline

  • Service utilization for reproductive health issues

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions and group discussion (open-ended questions) with healthcare providers, stakeholders and policymakers

    Baseline

  • Career-related impact of reproductive health issues of female serving in the CAF

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions

    Baseline

  • Recommendations and support services for improving female reproductive care within the CAF

    Assessed using a self-administered, pan-Canadian online questionnaire with multiple-choice response options and semi-structured individual interviews with open-ended questions and group discussion (open-ended questions) with healthcare providers, stakeholders and policymakers

    Baseline

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All female individuals serving in the CAF and Veterans will be included in part 1. Part 2 will include female individuals having experienced a reproductive health issue while serving in the CAF. Part 3 will include clinicians, stakeholders and policymakers who care for or support reproductive health of female CAF members (active duty and Veterans).

You may qualify if:

  • Female (biological sex)
  • Aged at least 18 years old
  • Completed Basic Military Qualification (including Regular Forces, Reserve Forces (Class A, B, or C), Canadian Rangers, COATS instructors, and survivors of the LGBT Purge whose official records of service have been changed to reflect the nature of their discharge)
  • Female (biological sex)
  • Aged at least 18 years old
  • Completed Basic Military Qualification (including Regular Forces, Reserve Forces (Class A, B, or C), Canadian Rangers, COATS instructors, and survivors of the LGBT Purge whose official records of service have been changed to reflect the nature of their discharge)
  • Have experienced a reproductive health issue while serving in the CAF
  • Healthcare providers (CAF Health Services, public servant, civilian) who has treated female patients who are actively serving and/or Veterans of the CAF in the past 5 years.
  • Stakeholders who are involved in supporting reproductive health of female members of the CAF and/or Veterans.
  • Policymakers who are involved in supporting reproductive health of female members of the CAF and/or Veterans.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre hospitalier universitaire de Sherbrooke

Sherbrooke, Quebec, J1H 5N4, Canada

Location

Related Links

MeSH Terms

Conditions

Infertility

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Study Officials

  • Mélanie Morin, PhD

    PT, PhD, Full professor, Researcher, Director of the Pelvic Health Research Laboratory, Canada Research Chair in Women's pelvic health, Faculty of Medicine and Health Sciences, University of Sherbrooke and Research Centre of the CHUS

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PT, PhD, Full professor, Researcher, Director of the Pelvic Health Research Laboratory, Canada Research Chair in Women's pelvic health, Faculty of Medicine and Health Sciences, University of Sherbrooke and Research Centre of the CHUS

Study Record Dates

First Submitted

April 1, 2026

First Posted

April 13, 2026

Study Start

April 15, 2026

Primary Completion (Estimated)

December 15, 2026

Study Completion (Estimated)

December 15, 2026

Last Updated

April 13, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Due to the nature of the participant population (active-duty military personnel and Veterans) and confidential information, individual data will not be shared. Only deanonymized and aggregated data will be shared with the scientific population and/or other organizations, upon request.

Locations