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The Experience of Living With Polycystic Ovary Syndrome in the Military

The Experience of Living With Polycystic Ovary Syndrome in the Military

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03876665
Acronym
PCOS
Enrollment
24
Registered
2019-03-15
Start date
2019-08-15
Completion date
2020-12-30
Last updated
2021-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome

Keywords

Polycystic Ovary Syndrome, Military, Service Women, Active Duty

Brief summary

The purpose of this study is to understand the experience of living with polycystic ovary syndrome (PCOS) as an active duty Service Woman. As part of a budding research program, this proposed study will lay the groundwork for future intervention studies targeting the management of PCOS in a military population.

Detailed description

Using a qualitative descriptive approach with focus groups (FG) and individual interviews (II), the investigators will seek to describe the experience of living with PCOS as an active duty service woman (ADSW). This method will allow the investigators to obtain a comprehensive summary of living with PCOS in the every day terms of ADSW. The discussion in the (FG) meetings will be an effective way to supply information about what people think, or how they feel, or on the way they act. Advantages of this method include: (a) it can cover a large number of people in one session, (b) it is an efficient way of gaining a large amount of information in a short time, (c) it is comparatively easier to drive or conduct, and (d) it generates an opportunity to collect data from the group interaction, which concentrates on the topic of the researcher's interest \[64, 65\]. This proposed study will focus on six primary areas of inquiry: (a) experience of receiving PCOS diagnosis (b) symptoms experienced and methods of coping with them, (c) military-specific experience of managing and living with PCOS, (d) access to/availability of information related to PCOS and how they have applied it, (e) experience of support, and (f) present and future concerns about having PCOS.

Interventions

OTHERNo intervention

No intervention

Sponsors

Madigan Army Medical Center
CollaboratorFED
United States Naval Medical Center, San Diego
CollaboratorFED
Malcolm Grow Medical Clinics and Surgery Center
CollaboratorFED
David Grant U.S. Air Force Medical Center
Lead SponsorFED

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women, active duty or prior (within 5 years) in the Army, Navy, Air Force or Marine Corps * Diagnosed with PCOS * 18 years of age or over

Exclusion criteria

* Reservist, Coast Guard, women who have separated or retired \> 5 years ago

Design outcomes

Primary

MeasureTime frameDescription
Describe the PCOS experience of active duty service membersthrough study completion, up to 18 monthsInformation from focused groups (FG) discussions and individual interviews (II) will be transcribed, categorized and then organized into themes that describe the experiences of active duty service members
Describe the PCOS experience by branch of servicethrough study completion, up to 18 monthsInformation from focused groups (FG) discussions and individual interviews (II) will be transcribed, categorized and then organized into themes that describe the experiences by branch of service

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026