Opinion of Brazilian Gynecologists on Hormone Therapy for Menopause and Prescriptive Habits

September 28, 2021 updated by: Luciano de Melo Pompei', Faculdade de Medicina do ABC

Opinion of Brazilian Gynecologists on Hormone Therapy for Menopause and Prescriptive

To evaluate Brazilian gynecologists, through structured online questionnaires, with questions directed to their opinions and prescriptive habits about menopause hormone therapy. Research participants will complete the questionnaires in digital format online.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

There are few Brazilian population studies on the opinion of Brazilian gynecologists about the hormonal therapy of menopause in climacteric women, their prescriptive habits and their views on the availability of treatments offered, demanding better evaluation and justifying efforts to analyze the perception of professionals in this area in our country.

Methods: To assess gynecologists across the country, through structured online questionnaires, with questions aimed at knowing their opinions and prescriptive habits about menopause hormone therapy. Research participants will complete the questionnaires in digital format online. Doctors will be invited to participate by e-mail messages and by social media.

Study Type

Observational

Enrollment (Actual)

1339

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • SP
      • São Bernardo do Campo, SP, Brazil, 09760-280
        • Centro de Atenção Integral à Saúde da Mulher

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Active Brazilian licensed gynecologist doctors who see patients

Description

Inclusion Criteria:

  • Brazilian licensed gynecologist doctors

Exclusion Criteria:

  • Retired doctors
  • Health professionals other than medicine doctor
  • Medical specialties other than Gynecology
  • Medical employees of the pharmaceutical industry

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Gynecologists
Brazilian gynecologists who agreed to participate and answered the questionnaire
The participants have to answer a questionnaire addressing their opinion on menopausal hormone replacement therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prescription preference
Time Frame: At Day 1
Answer to the questionnaire addressing gynecologists' prescription habit for menopausal women
At Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge of window of opportunity for hormone replacement therapy
Time Frame: At Day 1
This is to see which proportion of gynecologists know the principle of window of opportunity for menopausal hormone replacement therapy
At Day 1
Knowledge of indications and contraindications of hormone replacement therapy
Time Frame: At Day 1
This is to see which proportion of gynecologists know the indications and contraindicationsv of menopausal hormone replacement therapy
At Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 28, 2021

Primary Completion (Actual)

September 4, 2021

Study Completion (Actual)

September 4, 2021

Study Registration Dates

First Submitted

September 17, 2021

First Submitted That Met QC Criteria

September 28, 2021

First Posted (Actual)

October 11, 2021

Study Record Updates

Last Update Posted (Actual)

October 11, 2021

Last Update Submitted That Met QC Criteria

September 28, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 40147120.8.0000.0082

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

This is not an interventional study, so, the researches understand that there is no reason to share individual participant data.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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