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Postmenopausal clinical trials

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NCT ID: NCT06228768 Recruiting - Breast Cancer Clinical Trials

Acupressure for Aromatase Inhibitor-Associated Musculoskeletal Symptoms in Patients With Breast Cancer

Start date: March 2024
Phase: N/A
Study type: Interventional

This is a randomized, double-blinded trial of self-acupressure to examine the effect of treatment on aromatase inhibitor (AI)-associated musculoskeletal symptoms (AIMSS) in postmenopausal women with breast cancer. Acupressure is similar to acupuncture, but uses pressure rather than needles to stimulate specific points on the body. Acupressure involves applying mild to moderate physical pressure using your fingers, or an assistive device, to these points to try to bring about a physiological change in your body, in this case relief from joint pain and stiffness. The investigators will also examine effects of acupressure on other symptoms that commonly develop in AI-treated patients. In addition, changes in stool microbiome with acupressure treatment will be examined in an exploratory way to obtain preliminary information about the effect of acupressure on the gut microbiome in this condition.

NCT ID: NCT05998460 Not yet recruiting - Prediabetes Clinical Trials

Glucose-Guided Eating Pilot

GET CHARGED
Start date: January 2, 2024
Phase: N/A
Study type: Interventional

This is a single center, parallel-arm randomized controlled pilot study that aims to examine the feasibility and acceptability of the glucose-guided eating (GGE) mobile app and intervention in two populations at risk of chronic disease (postmenopausal women with prediabetes and AYA cancer survivors).

NCT ID: NCT05590507 Completed - Postmenopausal Clinical Trials

Remote Mindfulness-Based Physical Activity Intervention for Postmenopausal Women

Start date: December 28, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to figure out if postmenopausal women find a mindfulness audio recording acceptable for use along with physical activity, and to find out if this tool is helpful in increasing daily physical activity.

NCT ID: NCT05544357 Active, not recruiting - Hypertension Clinical Trials

Cardiovascular Adaptations to Resistance Exercise: Effect of Set Configuration on Postmenopausal Women

CARE
Start date: February 3, 2023
Phase: N/A
Study type: Interventional

The main purpose of this project is to analyze the effect of set configuration of resistance exercise on cardiovascular responses and adaptations of postmenopausal women. Additionally, since previous studies have shown that individual´s blood pressure level can influence on the impact of resistance training programs on cardiovascular changes, we aim to contrast acute and chronic changes to resistance training programs in normotensive and hypertensive postmenopausal women.

NCT ID: NCT05352516 Active, not recruiting - Postmenopausal Clinical Trials

A Study to Evaluate the Efficacy and Safety of HLX14 vs. Denosumab Prolia® in Postmenopausal Women With Osteoporosis at High Risk of Fracture

Start date: June 17, 2022
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, international multicentre, parallel-controlled phase III clinical study. The study plans to enroll 478 postmenopausal women with osteoporosis at high risk of fracture, whom will be randomized at 1:1 to either the experiment group (HLX14) or the control group (Prolia®) based on stratification factors (BMI (< 25, 25-30, > 30) and geographic region (Asian or non-Asian)). The study includes screening period (28 days), treatment period (total 546 days, contain treatment period 1: D1-D364, treatment period 2: D365-D546), and an end-of-study visit (D547).

NCT ID: NCT05009238 Not yet recruiting - Postmenopausal Clinical Trials

Effect of l S Exercises on Balance and Spatiotemporal Gait Parameters in P M Women

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Menopause is a natural process in women's life with hormonal fluctuations that cause physical and emotional symptoms such as(Hot flashes, insomnia, physical in activity, unstable mood, difficulties in memory and concentration, anxiety, stress, irritability, unstable body mass, sexual dysfunction, feelings of sadness, infertility, and depression). Balance disturbances are common in the community as a whole and increase in frequency with age. The risk of falling increases from age 45 in women and peaks in the 55-59-year age group. Around the time of the menopause, estrogen production decreases dramatically and bone loss accelerates, which predisposes for fractures if a fall occurs.

NCT ID: NCT04705623 Recruiting - Postmenopausal Clinical Trials

Influence of Iyengar Yoga on the Bio-functional Age of Postmenopausal Women

IIYBFAPW
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this Study is to find out if Iyengar-Yoga has a rejuvenating effect on women after menopause. The biofunctional status of the study participants will be assessed before and after a 12-week yoga program.

NCT ID: NCT04364061 Completed - Overweight Clinical Trials

Post Exercise Substrate Oxidation, Appetite and Energy Intakes in Overweight/Obese Postmenopausal Women (EScAPE)

EScAPE
Start date: November 1, 2019
Phase: N/A
Study type: Interventional

High-intensity interval exercise (HIIT), as compared to moderate intensity continuous training (MICT), is a time-efficient strategy to decrease total and abdominal fat mass (FM). However, the mechanisms underlying such adaptations are not yet elucidated and research are still needed to establish the optimal HIIT according to subject characteristics. The aim of this study was to compare acute HIIE and MICE cycling exercises on enjoyment, post-exercise substrate oxidation, appetite and energy intakes over 24h in postmenopausal women with overweight or obesity. It is hypothesized that compared with the traditional MICE, HIIE could favor greater enjoyment, higher 2h-post-exercise fat oxidation and a similar energy intakes over 24h despite different post-exercise appetite perceptions.

NCT ID: NCT04015544 Completed - Clinical trials for Overweight and Obesity

Markers of Atherosclerosis in Overweight, Postmenopausal Women Following Daily Watermelon Consumption

Start date: April 2014
Phase: N/A
Study type: Interventional

The primary purpose of this study is to determine the effectiveness of six weeks of watermelon puree supplementation, compared to control (no treatment), on blood antioxidant capacity, inflammation markers in the blood, biomarkers of metabolism in the blood, and cardiovascular disease markers in the blood, and biomarkers in the blood related to watermelon ingestion in overweight post-menopausal women. The secondary purpose is to compare body composition and body mass between the watermelon supplement group and the control group.

NCT ID: NCT03953157 Recruiting - Clinical trials for Anatomic Stage II Breast Cancer AJCC v8

Dietary and Exercise Interventions in Reducing Side Effects in Patients With Stage I-IIIa Breast Cancer Receiving Aromatase Inhibitors

Start date: October 7, 2019
Phase: N/A
Study type: Interventional

This phase I/II trial studies how well dietary and exercise interventions work in reducing side effects in patients with stage I-IIIa breast cancer taking aromatase inhibitors. Anti-inflammatory Mediterranean dietary and bone strengthening exercise interventions may alleviate medication side effects such as joint and bone pain and protectively influence bone mineral density, improve heart functioning, and reduce risk of breast cancer recurrence in breast cancer patients taking aromatase inhibitors.