Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID07524764

Female Reproductive Health in Canadian Armed Forces: Experience, Access to Care, and Support

Led by Université de Sherbrooke · Updated on 2026-05-22

1121

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

Université de Sherbrooke

Lead Sponsor

V

Veterans Affairs Canada

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying reproductive health among female members and Veterans of the Canadian Armed Forces (CAF). The study explores four main areas: contraception, undesired reproductive outcomes like unintended pregnancy and infertility, assisted reproductive care, and pelvic floor dysfunctions. It also examines related factors such as gynecological health, including menstrual health and sexually transmitted infections, as well as physical and psychological health conditions like depression and post-traumatic stress disorder. The findings aim to guide improvements in reproductive health care within the CAF. The project consists of three parts. First, an online survey will collect data from at least 1067 female CAF members and Veterans. Second, individual interviews will be conducted with about 30 female participants who have experienced reproductive health issues. Third, group discussions will involve 24 healthcare providers, stakeholders, and policymakers who work with or support female CAF members and Veterans. Recruitment efforts will ensure diverse representation across military roles, minority groups, and languages (English and French). Participants will provide information about their reproductive health experiences, risk factors, care access, and career impacts. Researchers will analyze service use and identify barriers and facilitators to care. The study will also gather recommendations to improve support services. Data collection includes surveys, interviews, and group discussions, focusing on lived experiences and care challenges. The study is observational, with participation lasting according to each part's design, starting in May 2026 and ending in December 2026.

CONDITIONS

Brief Title

Female Reproductive Health in Canadian Armed Forces

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female (biological sex)
  • At least 18 years old
  • Completed Basic Military Qualification, including Regular Forces, Reserve Forces, Canadian Rangers, COATS instructors, and survivors of the LGBT Purge
  • For interviews: Must have experienced a reproductive health issue while serving in the Canadian Armed Forces
  • For group discussions: Healthcare providers, stakeholders, or policymakers involved in female reproductive health care for Canadian Armed Forces members or Veterans
Not Eligible

You will not qualify if you...

  • Male biological sex
  • Under 18 years old
  • Not completed Basic Military Qualification in the Canadian Armed Forces or related groups
  • For interviews: No experience of reproductive health issues while serving in the Canadian Armed Forces
  • For group discussions: Not a healthcare provider, stakeholder, or policymaker involved in female reproductive health care for Canadian Armed Forces members or Veterans

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Diagnostic Evaluation

Duration - Single session during baseline assessment

Participants share their experiences and information regarding female reproductive health issues and related factors.

1 visit (in-person or remote)

Long-term Monitoring

Duration - Up to study completion in December 2026

Participants' reproductive health and access to care are observed over time to understand ongoing impacts and support needs.

Periodic follow-up contacts as scheduled by the study team

Trial Site Locations

Total: 1 location

1

Centre hospitalier universitaire de Sherbrooke

Sherbrooke, Quebec, Canada, J1H 5N4

Actively Recruiting

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Research Team

C

Chris M Edwards, PhD

C

Camille Simard, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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