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Clinical Trials/NCT00345072
NCT00345072
Unknown
Not Applicable

A Menopause Interactive Decision Aid System

Rhode Island Hospital2 sites in 1 country296 target enrollmentJuly 2003
ConditionsMenopause

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Menopause
Sponsor
Rhode Island Hospital
Enrollment
296
Locations
2
Primary Endpoint
Decisional conflict
Last Updated
19 years ago

Overview

Brief Summary

The purpose of this study is to develop and test a web-based system intended to help women going through menopause make more informed choices regarding menopause treatments. The system will do this by giving women personalized feedback on the risks and benefits of these treatments.

Detailed Description

Most women are not satisfied with the counseling they receive about menopause. To improve menopause counseling and help menopausal women more actively participate in the decision making process, we have developed a novel prototype web-based decision aid. Our immediate goal is to develop this prototype technology into a comprehensive Menopause Interactive Decision Aid System (MIDAS) that provides personalized feedback about menopausal symptoms, risks for common conditions, and the effects of different treatment options on the short- and long-term consequences of menopause. Our main study hypotheses are that MIDAS can: 1) lead to better decisions and improve the quality of menopausal counseling; 2) improve compliance with a chosen menopausal plan; and 3) reduce medical errors associated with the use of menopausal therapies. We propose a 2-phase study conducted over 3 years. Phase I will transform the prototype application into a comprehensive MIDAS, completing its content and risk assessment instruments, and exploring its optimal design. This will be accomplished through conduct of focus groups and usability tests. Phase II will formally evaluate the impact of MIDAS in a randomized, controlled, multi-center clinical trial involving diverse patient populations and clinician settings. We will measure the impact of MIDAS on the decision-making process as well as its effect on providers and outcome measures related to menopause, including compliance, quality of life, and medical errors related to menopausal therapy. Analyses will evaluate the extent to which the impact of MIDAS on these outcomes varies according to patient, practice, and physician characteristics.

Registry
clinicaltrials.gov
Start Date
July 2003
End Date
TBD
Last Updated
19 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • English-speaking
  • Between 45 and 65 years of age
  • Patient at participating clinics
  • Experience menopausal symptoms or being 6 months or more past last menstrual period
  • Have an upcoming appointment for menopausal counseling or annual physical exam (only applicable for clinical trial participants)

Exclusion Criteria

  • Inability to give informed consent
  • Age over 65 years
  • Pre-existing terminal illness that limits life expectancy to less than 2 years
  • History of breast cancer or cardiovascular disease

Outcomes

Primary Outcomes

Decisional conflict

Knowledge of the benefits, risks and side effects of menopausal treatments

Risk perception for breast cancer, CHD, and hip fracture

Patient-physician communication

Satisfaction with decision

Anxiety

Depression

Quality of menopausal counseling

Adherence to medication and lifestyle changes

Health-related quality of life

Menopause-specific quality of life

Study Sites (2)

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