Program to help women manage menopausal symptoms
Effectiveness of a Combined Education and Exercise Program on the Physical, Functional and Psychological Status of Climacteric Women.
NA · University of Valencia · NCT06419972
This study tests a program that helps women manage their menopausal symptoms through exercise and education to improve their overall well-being.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 115 (estimated) |
| Ages | 45 Years to 85 Years |
| Sex | Female |
| Sponsor | University of Valencia (other) |
| Locations | 2 sites (Valencia and 1 other locations) |
| Trial ID | NCT06419972 on ClinicalTrials.gov |
What this trial studies
This program focuses on non-pharmacological and non-hormonal approaches to manage menopausal symptoms in climacteric women. It emphasizes muscle training and education to improve physical well-being and psychological support during the menopausal transition. The program recognizes that each woman's experience is unique and aims to provide tailored interventions to enhance quality of life. Participants will engage in a multimodal physiotherapy program designed to address various symptoms associated with menopause.
Who should consider this trial
Good fit: Ideal candidates for this program are women aged 45 and older who are in the climacteric period.
Not a fit: Patients with significant musculoskeletal, cognitive, infectious, neurological, or cardiorespiratory issues may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly improve the quality of life for women experiencing menopausal symptoms.
How similar studies have performed: Other studies have shown success with non-pharmacological approaches to managing menopausal symptoms, indicating potential for this program.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women aged ≥45 years * Women in climacteric period Exclusion Criteria: * Musculoskeletal, cognitive, infectious, neurological, or cardiorespiratory pathology impairing assessment or program completion. * Surgical intervention in lumbopelvic or gynecological region within the last 6 months. Undergoing oncological treatment. \* Also included women with stable hormone replacement therapy for at least the last 6 months.
Where this trial is running
Valencia and 1 other locations
- Department of Physiotherapy. University of Valencia — Valencia, Spain (RECRUITING)
- Laura Fuentes Aparicio — Valencia, Spain (NOT_YET_RECRUITING)
Study contacts
- Study coordinator: Laura Fuentes-Aparicio, PhD
- Email: laura.fuentes@uv.es
- Phone: 669682391
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Climacteric Syndrome, Postmenopausal Symptoms, Menopause, Perimenopausal Disorder, perimenopause, climacteric, Postmenopause, women's health