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MyHealtheVet to Enable Shared Decision Making Regarding Menopausal in Postmenopausal Women Veterans (MEANS)

Not Applicable
Completed
Conditions
Menopause
Interventions
Other: Menopause educational secure messaging
Registration Number
NCT03109145
Lead Sponsor
Miami VA Healthcare System
Brief Summary

The purpose of this research study is to examine the impact of educational secure messages on menopause. In particular, the investigators will examine whether the secure messages increase menopause knowledge and communication between patients and their providers.

Detailed Description

The overall goal of this project is to determine the effectiveness of the MEANS (MyHealtheVet to Enable And Negotiate for Shared decision making) intervention in improving women's self-reported knowledge and rates of diagnosis and appropriate management of menopause symptoms. The proposed intervention is an educational and shared decision making platform for menopause symptoms to improve communication between patients and their providers regarding menopause symptoms. MEANS combines educational secure messages through the Veterans Affairs online Personal Health Record called MyHealtheVet, along with face-to-face and print interventions.

MEANS will be applied in target population consisting of postmenopausal women Veterans ages 45 to 60 who receive primary care at the Miami Veterans Affairs Healthcare System. This project will enroll women in MyHealtheVet, develop a library of menopause symptoms material for distribution, and evaluate how useful of MyHealtheVet use for educating and tracking women regarding menopause symptoms.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
859
Inclusion Criteria
  • Women Veterans, age 45-60
  • Receive primary care at the Miami Veterans Affairs Healthcare System
  • Able to communicate in English
  • Already or willing to register and become authenticated in the patient health portal, MyHealtheVet.
  • Able to use read, understand, and respond to secure messages using patient health portal.
Exclusion Criteria
  • Not willing to register and become authenticated for patient health portal.
  • Not willing to receive educational secure messages from patient health portal.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Menopause educational secure messagingMenopause educational secure messagingSecure messages that provide information about menopause and treatment option for menopause symptoms.
Primary Outcome Measures
NameTimeMethod
Feasibility of patient portal use for educating and tracking women regarding menopause and menopause related symptoms.6-months

The study will send weekly secure messages regarding menopause, and ask participants to report their menopause related symptoms by secure messaging. The research study will track the number of times participants read the weekly information sent via MyHealtheVet and the proportion of times they respond.

Menopause Knowledge6-months

Total menopause knowledge score (a) before and after the intervention, an average of 6-months and (b) compared to a control group of eligible women patients between 45-60 years who do not receive the intervention at the West Palm Beach and Orlando Veterans Healthcare System. Score is the percent of knowledge questions answered correctly (0 - 100%)

Secondary Outcome Measures
NameTimeMethod
Shared decision makingThrough study completion, an average of 3-years

Self-reported rate of shared decision making among women veteran and their providers.

Menopause related diagnosisThrough study completion, an average of 3-years

Rates of diagnosis and appropriate management of menopause related symptoms and use of hormone therapy.

Focus Group6-months

Qualitative assessment of the interventions through participant semi-structure focus group interviews.

Patient portal registration and authenticationThrough study completion, an average of 3-years

Measure the number of eligible women patients in the Miami Veterans Healthcare System who are enrolled and authenticated in the patient portal before and after the intervention.

Trial Locations

Locations (1)

Miami Veterans Affairs Healthcare System

🇺🇸

Miami, Florida, United States

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