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Breast Neoplasms clinical trials

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NCT ID: NCT04316156 Completed - Breast Cancer Clinical Trials

Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial

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

This study aims to examine the effect of hospital-home linkage short-term rehabilitation therapy using real-time interactive digital healthcare system (Uincare Homeplus) in post-operative patients with breast cancer. This is prospective study. 100 breast cancer patients who underwent axillary lymph node diessection or breast reconstruction following mastectomy will be examined, and those with limited range of motion (ROM) of affected shoulder will be enrolled in the study. Shoulder ROM, Quick-DASH, pain evaluation with NRS, quality of life evaluation with FACT-B and EQ-5D will be evaluated on enrollment, 4-week, 8-week, and 12-weeks after enrollment.

NCT ID: NCT04315012 Completed - Breast Cancer Clinical Trials

Training With Mobile Application in Breast Cancer

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Endocrine hormonal therapy (EHT) applied to avoid recurrence and metastasis of the breast cancer has also side effects which do not threaten life; however, it does negatively effects quality of life. The objective of this study was to determine the effects on quality of life of a mobile app-based (e-mobile) education for supportive care of patients with breast cancer receiving adjuvant endocrine hormonal therapy. The data were collected to with face to face and/or telephone interviews at 2 time points: prior to the initiation (T0) and after the completion (T1) of mobile app-based education. Patients were received education via mobile app for 12 weeks during which they were contacted in every 15 days; a mobile app-based (e-mobile) education was provided, including information about breast cancer definition, treatment process, symptoms management, adequate nutrition, regular physical activity and coping with stress. In this process, the control group patients were provided with standard care.

NCT ID: NCT04312347 Completed - ER+ Breast Cancer Clinical Trials

Tamoxifen Dose Adjustment on Indonesian Female ER+ Breast Cancer Patients Based on CYP2D6 Genotype and Endoxifen Levels

Start date: September 6, 2019
Phase: N/A
Study type: Interventional

The objectives of this study is to perform CYP2D6 genotyping and metabolite concentrations analysis on ER+ breast cancer patients who are taking tamoxifen and give dose recommendations based on the CYP2D6 genotypes and endoxifen levels.

NCT ID: NCT04307407 Completed - Breast Cancer Clinical Trials

Exercise in Breast Cancer Survivors

Start date: September 8, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of aerobic exercise to usual care in women treated with chemotherapy and radiation therapy for non-metastatic breast cancer

NCT ID: NCT04306003 Completed - Breast Cancer Clinical Trials

ERAS in Autologous Breast Reconstruction: A Pilot RCT

ERAS-ABR
Start date: November 5, 2019
Phase: N/A
Study type: Interventional

Over 26,000 Canadian women are diagnosed with breast cancer each year and 1 in 3 patients undergo mastectomy. With an upward of 40% of breast cancer patients seeking post-mastectomy breast reconstruction (PMBR), there is a significant opportunity to improve the quality of perioperative care for breast reconstruction patients. Enhanced Recovery After Surgery (ERAS) is a multidisciplinary, multimodal, and evidence-based approach to perioperative care that safely reduces hospital length of stay and opioid use following colorectal surgery. ERAS recommendations have been proposed for women undergoing autologous PMBR who typically stay in hospital 4 to 5 days after surgery. However, the evidence to support ERAS in breast reconstruction is limited to observational studies compared to the numerous clinical trials in colorectal surgery. The goal of this study is to address this knowledge gap by evaluating the feasibility of conducting a RCT comparing ERAS to standard perioperative care.

NCT ID: NCT04304404 Completed - Breast Cancer Clinical Trials

Risk Reduction Program for Women Having High Risk of Breast Cancer

BrCaRRP
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

An intervention program involving education, guidance, counseling, case management and surveillance based on the Health Belief Model will be implemented on women with high risk of breast cancer. The impact of the breast cancer risk reduction program on participation in breast cancer screenings, health beliefs (health motivation, sensitivity, fear of breast cancer) and behaviors (physical activity, nutrition, health responsibility, genetic counseling) will be evaluated in the study.

NCT ID: NCT04300478 Completed - Breast Cancer Clinical Trials

Appetite and Exercise in Breast Cancer Survivors

EARNESt
Start date: February 7, 2020
Phase: N/A
Study type: Interventional

The overall aim of this research is to investigate the acute effects of resistance exercise (REx) on the hormonal and behavioral indices of energy balance regulation in breast cancer survivors. This pilot study is designed to provide preliminary data to support future exercise interventions with more comprehensive energy balance profiling.

NCT ID: NCT04300283 Completed - Clinical trials for Breast Cancer Surgery

Pre-operative Hypnosis to Prevent Side Effects After Surgery

PREVENTpilot
Start date: May 1, 2018
Phase: N/A
Study type: Interventional

The aim of the pilot study is to translate and feasibility test a brief hypnosis intervention in 8-10 patients that are about to undergo thoracic surgery and in 4-5 patients about to undergo breast cancer surgery.

NCT ID: NCT04298333 Completed - Clinical trials for Metastatic Breast Cancer

Dose-finding Study of BP-C1 in Patients With Stage IV Breast Cancer

Start date: June 27, 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to estimate the cumulative Maximum Tolerated Dose (MTD) and Minimum Efficient Dose (MED) of BP-C1 in the short-term treatment of metastatic breast cancer patients.

NCT ID: NCT04297657 Completed - Breast Cancer Clinical Trials

Using BETTER Model Sexual Problems in Breast Cancer

Start date: April 28, 2016
Phase: N/A
Study type: Interventional

Breast cancer and its treatments such as mastectomy, chemotherapy, radiotherapy, hormonal therapy cause many side effects such as scar, problems with body perception and sexual problems. Sexual concerns lead to significant emotional distress, including sadness/depression, issues related to personal appearance, stigma, and negative impacts on personal relationships, intimacy and sexuality all of which reduce the quality of life. This experimental type of research is conducted within the framework of the BETTER model to evaluate the impact of counselling programme on sexuality issues that patients with breast cancer experience.