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"Menopause Experiences in Cultural and Intercultural Contexts"

NCT07648680 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2026-06-15

No results posted yet for this study

Summary

The climacteric period involves physical, hormonal, and emotional changes that can impact a woman's quality of life. This mixed-methods study aims to explore the perceptions and experiences of women during menopause and the influence of cultural ethnicity on their quality of life in Primary Care centers in Tarragona. The research includes a quantitative phase to assess healthcare professionals' knowledge via electronic surveys and a qualitative phase using individual interviews with women from diverse backgrounds. The goal is to identify specific needs to adapt community nursing interventions and improve health promotion and equity during the climacteric stage.

Conditions

  • Valid MeSH Conditions

Interventions

BEHAVIORAL

Survey and Semi-structured Interview

For Professionals: An electronic questionnaire to assess knowledge and attitudes toward menopause. For Women: A qualitative semi-structured interview to explore their perceptions and lived experiences during the climacteric stage.

Sponsors & Collaborators

  • Institut Investigacio Sanitaria Pere Virgili

    lead OTHER

Principal Investigators

  • Rosa Raventós Torner, RN, MSN, PhD · Universidad Rovira i Virgili

  • Cristina Rey Reñones, RN, MSN, PhD · Universidad Rovira Y Virgili

  • Rocío Legaz Pagán, PhD Student, RN, MSc · Universidad Rovira Y Virgili

  • Marina Gómez de Quero Cordoba, RN, MSN, PhD · Universidad Rovira Y Virgili

Eligibility

Min Age
40 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-27
Primary Completion
2028-04-22
Completion
2030-04-22

Countries

  • Spain

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07648680 on ClinicalTrials.gov